Federal Food, Drug, and Cosmetic Act As amended through December 31, 2004 (See note below)
Chapter I--Short Title Chapter II--Definitions Chapter III--Prohibited Acts and Penalties Chapter IV--Food Chapter V--Drugs and Devices:
Subchapter A--Drugs and Devices: Sections 501-510: Drugs and Devices Section 512: New Animal Drugs Sections 513-523: Medical Devices Subchapter B--Drugs for Rare Diseases and Conditions Subchapter C--Electronic Product Radiation Control Subchapter D--Dissemination of Treatment Information Subchapter E--General Provisions Relating to Drugs and Devices Subchapter F—New Animal Drugs for Minor Use and Minor Species
Chapter VI--Cosmetics Chapter VII--General Authority: Subchapter A--General Administrative Provisions Subchapter B--Colors Subchapter C--Fees Subchapter D--Information and Education Subchapter E--Environmental Impact Review Subchapter F--National Uniformity for Nonprescription Drugs and Preemption for Labeling or Packaging of Cosmetics Subchapter G--Safety Reports
Chapter VIII--Imports and Exports Chapter IX--Miscellaneous
Appendix: Section 107(c) of Drug Amendments of 1962 Public Law 88-136; Revolving Fund Section 108 of Animal Drug Amendments of 1968
Section 5 of Orphan Drug Act
Cross-reference of FD&C Act and U.S. Code section numbers
The FDA's online reference edition of the Federal Food, Drug and Cosmetic Act is based on the publication Compilation of Selected Acts Within the Jurisdiction of the Committee on Energy and Commerce; Food, Drug, and Related Law, As Amended Through December 31, 2004, prepared for the use of the Committee on Energy and Commerce, U.S. House of Representatives, March 2005. Some updates to the Act were incorporated in November 2007.
CHAPTER I— SHORT TITLE
Section 1 . [21 U.S.C. 301] This Act may be cited as the Federal Food, Drug, and Cosmetic
Act.
CHAPTER II—DEFINITIONS1
SEC. 201. [21 U.S.C. 321] For the purposes of this Act— 2
(a)(1) The term "State", except as used in the last sentence of section 702(a), means any
State or Territory of the United States , the District of Columbia , and the Commonwealth of
Puerto Rico .
(2) The term "Territory" means any Territory or possession of the United States , including the
District of Columbia , and excluding the Commonwealth of Puerto Rico and the Canal Zone.
(b) The term "interstate commerce" means (1) commerce between any State or Territory and
any place outside thereof, and (2) commerce within the District of Columbia or within any other
Territory not organized with a legislative body.
(c) The term "Department" means the Department of Health and Human Services.
(d) The term "Secretary" means the Secretary of Health and Human Services.
(e) The term "person" includes individual, partnership, corporation, and association.
(f) 1 The term "food" means (1) articles used for food or drink for man or other animals, (2)
chewing gum, and (3) articles used for components of any such article.
(g)(1) The term "drug" means (A) articles recognized in the official United States
Pharmacopeia, official Homeopathic Pharmacopeia of the United States, or official National
Formulary, or any supplement to any of them; and (B) articles intended for use in the diagnosis,
cure, mitigation, treatment, or prevention of disease in man or other animals; and (C) articles
(other than food) intended to affect the structure or any function of the body of man or other
animals; and (D) articles intended for use as a component of any articles specified in clause
(A), (B), or (C). A food or dietary supplement for which a claim, subject to sections 403(r)(1)(B)
and 403(r)(3) or sections 403(r)(1)(B) and 403(r)(5)(D), is made in accordance with the
requirements of section 403(r) is not a drug solely because the label or the labeling contains
such a claim. A food, dietary ingredient, or dietary supplement for which a truthful and not
misleading statement is made in accordance with section 403(r)(6) is not a drug under clause
(C) solely because the label or the labeling contains such a statement.
(2) The term "counterfeit drug" means a drug which, or the container or labeling of which,
without authorization, bears the trademark, trade name, or other identifying mark, imprint, or
device, or any likeness thereof, of a drug manufacturer, processor, packer, or distributor other
than the person or persons who in fact manufactured, processed, packed, or distributed such
drug and which thereby falsely purports or is represented to be the product of, or to have been
packed or distributed by, such other drug manufacturer, processor, packer, or distributor.
(h) The term "device" (except when used in paragraph (n) of this section and in sections 301(i),
403(f), 502(c), and 602(c)) means an instrument, apparatus, implement, machine, contrivance,
implant, in vitro reagent, or other similar or related article, including any component, part, or
accessory, which is—
(1) recognized in the official National Formulary, or the United States Pharmacopeia, or any
supplement to them,
(2) intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation,
treatment, or prevention of disease, in man or other animals, or
(3) intended to affect the structure or any function of the body of man or other animals, and
which does not achieve its primary intended purposes through chemical action within or on the
body of man or other animals and which is not dependent upon being metabolized for the
achievement of its primary intended purposes.
(i) The term "cosmetic" means (1) articles intended to be rubbed, poured, sprinkled, or sprayed
on, introduced into, or otherwise applied to the human body or any part thereof for cleansing,
beautifying, promoting attractiveness, or altering the appearance, and (2) articles intended for
use as a component of any such articles; except that such term shall not include soap.
(j) The term "official compendium" means the official United States Pharmacopeia, official
Homeopathic Pharmacopeia of the United States , official National Formulary, or any
supplement to any of them.
(k) The term "label" means a display of written, printed, or graphic matter upon the immediate
container of any article; and a requirement made by or under authority of this Act that any word,
statement, or other information appear on the label shall not be considered to be complied with
unless such word, statement, or other information also appears on the outside container or
wrapper, if any there be, of the retail package of such article, or is easily legible through the
outside container or wrapper.
(l) The term "immediate container" does not include package liners.
(m) The term "labeling" means all labels and other written, printed, or graphic matter (1) upon
any article or any of its containers or wrappers, or (2) accompanying such article.
(n) If an article is alleged to be misbranded because the labeling or advertising is misleading,
then in determining whether the labeling or advertising is misleading there shall be taken into
account (among other things) not only representations made or suggested by statement, word,
design, device, or any combination thereof, but also the extent to which the labeling or
advertising fails to reveal facts material in the light of such representations or material with
respect to consequences which may result from the use of the article to which the labeling or
advertising relates under the conditions of use prescribed in the labeling or advertising thereof
or under such conditions of use as are customary or usual.
(o) The representation of a drug, in its labeling, as an antiseptic shall be considered to be a
representation that it is a germicide, except in the case of a drug purporting to be, or
represented as, an antiseptic for inhibitory use as a wet dressing, ointment, dusting powder, or
such other use as involves prolonged contact with the body.
(p) 3 The term "new drug" means—
(1) Any drug (except a new animal drug or an animal feed bearing or containing a new animal
drug) the composition of which is such that such drug is not generally recognized, among
experts qualified by scientific training and experience to evaluate the safety and effectiveness
of drugs, as safe and effective for use under the conditions prescribed, recommended, or
suggested in the labeling thereof, except that such a drug not so recognized shall not be
deemed to be a "new drug" if at any time prior to the enactment of this Act it was subject to the
Food and Drugs Act of June 30, 1906, as amended, and if at such time its labeling contained
the same representations concerning the conditions of its use; or
(2) Any drug (except a new animal drug or an animal feed bearing or containing a new animal
drug) the composition of which is such that such drug, as a result of investigations to
determine its safety and effectiveness for use under such conditions, has become so
recognized, but which has not, otherwise than in such investigations, been used to a material
extent or for a material time under such conditions.
(q)(1)(A) Except as provided in clause (B), the term "pesticide chemical" means any substance
that is a pesticide within the meaning of the Federal Insecticide, Fungicide, and Rodenticide
Act, including all active and inert ingredients of such pesticide. Notwithstanding any other
provision of law, the term 'pesticide' within such meaning includes ethylene oxide and
propylene oxide when such substances are applied on food.
(B) In the case of the use, with respect to food, of a substance described in clause (A) to
prevent, destroy, repel, or mitigate microorganisms (including bacteria, viruses, fungi, protozoa,
algae, and slime), the following applies for purposes of clause (A):
(i) The definition in such clause for the term "pesticide chemical" does not include the
substance if the substance is applied for such use on food, or the substance is included for
such use in water that comes into contact with the food, in the preparing, packing, or holding of
the food for commercial purposes. The substance is not excluded under this subclause from
such definition if the substance is ethylene oxide or propylene oxide, and is applied for such
use on food. The substance is not so excluded if the substance is applied for such use on a
raw agricultural commodity, or the substance is included for such use in water that comes into
contact with the commodity, as follows:
(I) The substance is applied in the field.
(II) The substance is applied at a treatment facility where raw agricultural commodities are the
only food treated, and the treatment is in a manner that does not change the status of the food
as a raw agricultural commodity (including treatment through washing, waxing, fumigating, and
packing such commodities in such manner).
(III) The substance is applied during the transportation of such commodity between the field
and such a treatment facility.
(ii) The definition in such clause for the term "pesticide chemical" does not include the
substance if the substance is a food contact substance as defined in section 409(h)(6), and
any of the following circumstances exist: The substance is included for such use in an object
that has a food contact surface but is not intended to have an ongoing effect on any portion of
the object; the substance is included for such use in an object that has a food contact surface
and is intended to have an ongoing effect on a portion of the object but not on the food contact
surface; or the substance is included for such use in or is applied for such use on food
packaging (without regard to whether the substance is intended to have an ongoing effect on
any portion of the packaging). The food contact substance is not excluded under this
subclause from such definition if any of the following circumstances exist: The substance is
applied for such use on a semipermanent or permanent food contact surface (other than being
applied on food packaging); or the substance is included for such use in an object that has a
semipermanent or permanent food contact surface (other than being included in food
packaging) and the substance is intended to have an ongoing effect on the food contact
surface.
With respect to the definition of the term "pesticide" that is applicable to the Federal Insecticide,
Fungicide, and Rodenticide Act, this clause does not exclude any substance from such
definition.
(2) The term "pesticide chemical residue" means a residue in or on raw agricultural commodity
or processed food of—
(A) a pesticide chemical; or
(B) any other added substance that is present on or in the commodity or food primarily as a
result of the metabolism or other degradation of a pesticide chemical.
(3) Notwithstanding subparagraphs (1) and (2), the Administrator may by regulation except a
substance from the definition of "pesticide chemical" or "pesticide chemical residue" if—
(A) its occurrence as a residue on or in a raw agricultural commodity or processed food is
attributable primarily to natural causes or to human activities not involving the use of any
substances for a pesticidal purpose in the production, storage, processing, or transportation of
any raw agricultural commodity or processed food; and
(B) the Administrator, after consultation with the Secretary, determines that the substance
more appropriately should be regulated under one or more provisions of this Act other than
sections 402(a)(2)(B) and 408.
(r) The term "raw agricultural commodity" means any food in its raw or natural state, including
all fruits that are washed, colored, or otherwise treated in their unpeeled natural form prior to
marketing.
(s) The term "food additive" means any substance the intended use of which results or may
reasonably be expected to result, directly or indirectly, in its becoming a component or
otherwise affecting the characteristics of any food (including any substance intended for use in
producing, manufacturing, packing, processing, preparing, treating, packaging, transporting, or
holding food; and including any source of radiation intended for any such use), if such
substance is not generally recognized, among experts qualified by scientific training and
experience to evaluate its safety, as having been adequately shown through scientific
procedures (or, in the case of a substance used in food prior to January 1, 1958, through either
scientific procedures or experience based on common use in food) to be safe under the
conditions of its intended use; except that such term does not include—
(1) a pesticide chemical residue in or on a raw agricultural commodity or processed food; or
(2) a pesticide chemical; or
(3) a color additive; or
(4) any substance used in accordance with a sanction or approval granted prior to the
enactment of this paragraph 4 pursuant to this Act, the Poultry Products Inspection Act (21
U.S.C. 451 and the following) or the Meat Inspection Act of March 4, 1907 (34 Stat. 1260), as
amended and extended (21 U.S.C. 71 and the following);
(5) a new animal drug; or
(6) an ingredient described in paragraph (ff) in, or intended for use in, a dietary supplement.
(t)(1) The term "color additive" means a material which—
(A) is a dye, pigment, or other substance made by a process of synthesis or similar artifice, or
extracted, isolated, or otherwise derived, with or without intermediate or final change of identity,
from a vegetable, animal, mineral, or other source, and
(B) when added or applied to a food, drug, or cosmetic, or to the human body or any part
thereof, is capable (alone or through reaction with other substance) of imparting color thereto;
except that such term does not include any material which the Secretary, by regulation,
determines is used (or intended to be used) solely for a purpose or purposes other than
coloring.
(2) The term "color" includes black, white, and intermediate grays.
(3) Nothing in subparagraph (1) of this paragraph shall be construed to apply to any pesticide
chemical, soil or plant nutrient, or other agricultural chemical solely because of its effect in
aiding, re other natural physiological processes of produce of the soil and thereby affecting its
color, whether before or after harvest.
(u) The term "safe," as used in paragraph (s) of this section and in sections 409, 512, 571, and
721, has reference to the health of man or animal.
(v) The term "new animal drug" means any drug intended for use for animals other than man,
including any drug intended for use in animal feed but not including such animal feed—
(1) the composition of which is such that such drug is not generally recognized, among experts
qualified by scientific training and experience to evaluate the safety and effectiveness of
animal drugs, as safe and effective for use under the conditions prescribed, recommended, or
suggested in the labeling thereof; except that such a drug not so recognized shall not be
deemed to be a "new animal drug" if at any time prior to June 25, 1938, it was subject to the
Food and Drug Act of June 30, 1906, as amended, and if at such time its labeling contained
the same representations concerning the conditions of its use; or
(2) the composition of which is such that such drug, as a result of investigations to determine
its safety and effectiveness for use under such conditions, has become so recognized but
which has not, otherwise than in such investigations, been used to a material extent or for a
material time under such conditions.
Provided that 5 any drug intended for minor use or use in a minor species that is not the
subject of a final regulation published by the Secretary through notice and comment
rulemaking finding that the criteria of paragraphs (1) and (2) have not been met (or that the
exception to the criterion in paragraph (1) has been met) is a new animal drug.
(w) The term "animal feed", as used in paragraph (w) 6 of this section, in section 512, and in
provisions of this Act referring to such paragraph or section, means an article which is
intended for use for food for animals other than man and which is intended for use as a
substantial source of nutrients in the diet of the animal, and is not limited to a mixture intended
to be the sole ration of the animal.
(x) The term "informal hearing" means a hearing which is not subject to section 554, 556, or
557 of title 5 of the United States Code and which provides for the following:
(1) The presiding officer in the hearing shall be designated by the Secretary from officers and
employees of the Department who have not participated in any action of the Secretary which is
the subject of the hearing and who are not directly responsible to an officer or employee of the
Department who has participated in any such action.
(2) Each party to the hearing shall have the right at all times to be advised and accompanied
by an attorney.
(3) Before the hearing, each party to the hearing shall be given reasonable notice of the
matters to be considered at the hearing, including a comprehensive statement of the basis for
the action taken or proposed by the Secretary which is the subject of the hearing and a general
summary of the information which will be presented by the Secretary at the hearing in support
of such action.
(4) At the hearing the parties to the hearing shall have the right to hear a full and complete
statement of the action of the Secretary which is the subject of the hearing together with the
information and reasons supporting such action, to conduct reasonable questioning, and to
present any oral or written information relevant to such action.
(5) The presiding officer in such hearing shall prepare a written report of the hearing to which
shall be attached all written material presented at the hearing. The participants in the hearing
shall be given the opportunity to review and correct or supplement the presiding officer's report
of the hearing.
(6) The Secretary may require the hearing to be transcribed. A party to the hearing shall have
the right to have the hearing transcribed at his expense. Any transcription of a hearing shall be
included in the presiding officer's report of the hearing.
(y) The term "saccharin" includes calcium saccharin, sodium saccharin, and ammonium
saccharin.
(z) The term "infant formula" means a food which purports to be or is represented for special
dietary use solely as a food for infants by reason of its simulation of human milk or its suitability
as a complete or partial substitute for human milk.
(aa) The term "abbreviated drug application" means an application submitted under section
505(j) for the approval of a drug that relies on the approved application of another drug with the
same active ingredient to establish safety and efficacy, and—
(1) in the case of section 306, includes a supplement to such an application for a different or
additional use of the drug but does not include a supplement to such an application for other
than a different or additional use of the drug, and
(2) in the case of sections 307 and 308, includes any supplement to such an application.
(bb) The term "knowingly" or "knew" means that a person, with respect to information—
(1) has actual knowledge of the information, or
(2) acts in deliberate ignorance or reckless disregard of the truth or falsity of the information.
(cc) For purposes of section 306, the term "high managerial agent"—
(1) means—
(A) an officer or director of a corporation or an association,
(B) a partner of a partnership, or
(C) any employee or other agent of a corporation, association, or partnership, having duties
such that the conduct of such officer, director, partner, employee, or agent may fairly be
assumed to represent the policy of the corporation, association, or partnership, and
(2) includes persons having management responsibility for—
(A) submissions to the Food and Drug Administration regarding the development or approval
of any drug product, any drug product, or
(B) production, quality assurance, or quality control of any drug product, or
(C) research and development of any drug product.
(dd) For purposes of sections 306 and 307, the term "drug product" means a drug subject to
regulation under section 505, 512, or 802 of this Act or under section 351 of the Public Health
Service Act.
(ee) The term "Commissioner" means the Commissioner of Food and Drugs.
(ff) The term "dietary supplement"—
(1) means a product (other than tobacco) intended to supplement the diet that bears or
contains one or more of the following dietary ingredients:
(A) a vitamin;
(B) a mineral;
(C) an herb or other botanical;
(D) an amino acid;
(E) a dietary substance for use by man to supplement the diet by increasing the total dietary
intake; or
(F) a concentrate, metabolite, constituent, extract, or combination of any ingredient described
in clause (A), (B), (C), (D), or (E);
(2) means a product that—
(A)(i) is intended for ingestion in a form described in section 411(c)(1)(B)(i); or
(ii) complies with section 411(c)(1)(B)(ii);
(B) is not represented for use as a conventional food or as a sole item of a meal or the diet;
and
(C) is labeled as a dietary supplement; and
(3) does—
(A) include an article that is approved as a new drug under section 505 or licensed as a
biologic under section 351 of the Public Health Service Act (42 U.S.C. 262) and was, prior to
such approval, certification, or license, marketed as a dietary supplement or as a food unless
the Secretary has issued a regulation, after notice and comment, finding that the article, when
used as or in a dietary supplement under the conditions of use and dosages set forth in the
labeling for such dietary supplement, is unlawful under section 402(f); and
(B) not include—
(i) an article that is approved as a new drug under section 505, certified as an antibiotic under
section 507 7, or licensed as a biologic under section 351 of the Public Health Service Act (42
U.S.C. 262), or
(ii) an article authorized for investigation as a new drug, antibiotic, or biological for which
substantial clinical investigations have been instituted and for which the existence of such
investigations has been made public, which was not before such approval, certification,
licensing, or authorization marketed as a dietary supplement or as a food unless the Secretary,
in the Secretary's discretion, has issued would be lawful under this Act.
Except for purposes of section 201(g), a dietary supplement shall be deemed to be a food
within the meaning of this Act.
(gg) The term "processed food" means any food other than a raw agricultural commodity and
includes any raw agricultural commodity that has been subject to processing, such as canning,
cooking, freezing, dehydration, or milling.
(hh) The term "Administrator" means the Administrator of the United States Environmental
Protection Agency.
(ii) The term "compounded positron emission tomography drug"—
(1) means a drug that—
(A) exhibits spontaneous disintegration of unstable nuclei by the emission of positrons and is
used for the purpose of providing dual photon positron emission tomographic diagnostic
images; and
(B) has been compounded by or on the order of a practitioner who is licensed by a State to
compound or order compounding for a drug described in subparagraph (A), and is
compounded in accordance with that State's law, for a patient or for research, teaching, or
quality control; and
(2) includes any nonradioactive reagent, reagent kit, ingredient, nuclide generator, accelerator,
target material, electronic synthesizer, or other apparatus or computer program to be used in
the preparation of such a drug.
(jj) The term "antibiotic drug" means any drug (except drugs for use in animals other than
humans) composed wholly or partly of any kind of penicillin, streptomycin, chlortetracycline,
chloramphenicol, bacitracin, or any other drug intended for human use containing any quantity
of any chemical substance which is produced by a micro-organism and which has the capacity
to inhibit or destroy micro-organisms in dilute solution (including a chemically synthesized
equivalent of any such substance) or any derivative thereof.
(kk) 8 Priority Supplement- The term "priority supplement" means a drug application referred
to in section 101(4) of the Food and Drug Administration Modernization Act of 1997 (111 Stat.
2298).
(ll)(1) The term "single-use device" means a device that is intended for one use, or on a single
patient during a single procedure.
(2)(A) The term "reprocessed", with respect to a single-use device, means an original device
that has previously been used on a patient and has been subjected to additional processing
and manufacturing for the purpose of an additional single use on a patient. The subsequent
processing and manufacture of a reprocessed single-use device shall result in a device that is
reprocessed within the meaning of this definition.
(B) A single-use device that meets the definition under clause (A) shall be considered a
reprocessed device without regard to any description of the device used by the manufacturer
of the device or other persons, including a description that uses the term "recycled" rather than
the term "reprocessed".
(3) The term "original device" means a new, unused single-use device.
(mm)(1) The term "critical reprocessed single-use device" means a reprocessed single-use
device that is intended to contact normally sterile tissue or body spaces during use.
(2) The term "semi-critical reprocessed single-use device" means a reprocessed single-use
device that is intended to contact intact mucous membranes and not penetrate normally sterile
areas of the body.
(nn) The term "major species" means cattle, horses, swine, chickens, turkeys, dogs, and cats,
except that the Secretary may add species to this definition by regulation.
(oo) The term "minor species" means animals other than humans that are not major species.
(pp) The term "minor use" means the intended use of a drug in a major species for an
indication that occurs infrequently and in only a small number of animals or in limited
geographical areas and in only a small number of animals annually.
(qq) The term "major food allergen" means any of the following:
(1) Milk, egg, fish (e.g., bass, flounder, or cod), Crustacean shellfish (e.g., crab, lobster, or
shrimp), tree nuts (e.g., almonds, pecans, or walnuts), wheat, peanuts, and soybeans.
(2) A food ingredient that contains protein derived from a food specified in paragraph 9 (1),
except the following:
(A) Any highly refined oil derived from a food specified in paragraph (1) and any ingredient
derived from such highly refined oil.
(B) A food ingredient that is exempt under paragraph (6) or (7) of section 403(w).
Footnotes: Chapter II
1. The following additional definitions applicable to this Act are provided for in other Acts:
Butter. The Act of March 4, 1923 (21 U.S.C. 321a), defines butter as "the food product usually
known as butter, and which is made exclusively from milk or cream, or both, with or without
common salt, and with or without additional coloring matter, and containing not less than 80
per centum by weight of milk fat, all tolerances having been allowed for."
Package. The Act of July 24, 1919 (21 U.S.C. 321b), states "The word 'package' shall include
and shall be construed to include wrapped meats inclosed in papers or other materials as
prepared by the manufacturers thereof for sale."
Nonfat Dry Milk, Milk. The Act of July 2, 1956 (21 U.S.C. 321c), defines nonfat dry milk as "the
product resulting from the removal of fat and water from milk, and contains the lactose, milk
proteins, and milk minerals in the same relative proportions as in the fresh milk from which
made. It contains not over 5 per centum by weight of moisture. The fat content is not over 11⁄2
per centum by weight unless otherwise indicated.", and defines milk to mean sweet milk of
cows.
2. See footnote for section 403(h)(3) regarding the stylistic use of a list consisting of "(a)",
"(b)", etc.
3. The amendments made to this Act by the Drug Amendments of 1962 included amendments
establishing the requirement that new drugs be effective. Section 107(c) of such Public Law
concerned the applicability of the amendments, and is included in the appendix to this
compilation.
4. Paragraph (s) was added by Public Law 85–929, which was enacted September 6, 1958.
5. The proviso appears so as to reflect the probable intent of the Congress. See section
102(b)(5)(B) of Public Law 108–282, which in amending section 201(v) above referred to
"paragraph (2)" of the section. The reference probably should have been to "subparagraph (2)".
(See
footnote for section 403(h)(3) regarding the stylistic use of a list consisting of "(a)", "(b)", etc.)
With respect to the placement of the proviso, section 102(b)(5)(B) of such Public Law provided
for placement "after" paragraph (2) (not at the end of paragraph (2)), yet did not indicate
separate
indentation. The proviso has been placed after and below subparagraph (2), with separate
indentation, to indicate the probable intent of the Congress, although such placement of matter
that is not a complete sentence calls for striking the period at the end of subparagraph (2) and
inserting a semicolon, which section 102(b)(5)(B) of such Public Law did not do. (Compare
with
matter after and below section 201(t)(1)(B), for example.)
6. So in law. Probably should be paragraph "(v)".
7. So in law. Section 507 was repealed by section 125(b)(1) of Public Law 105–115 (111 Stat.
2325).
8. Indentation is so in law. See section 5(b)(1) of Public Law 107–109 (115 Stat. 1413).
9. So in law. See section 203(c)(1) of Public Law 108–282. Probably should be
"subparagraph". See footnote for section 403(h)(3).
CHAPTER III—PROHIBITED ACTS AND PENALTIES
PROHIBITED ACTS
SEC. 301. [ 21 U.S.C. 331] [Caution: See prospective amendment note below.] The
following acts and the causing thereof are hereby prohibited: 1
(a) The introduction or delivery for introduction into interstate commerce of any food, drug,
device, or cosmetic that is adulterated or misbranded.
(b) The adulteration or misbranding of any food, drug, device, or cosmetic in interstate
commerce.
(c) The receipt in interstate commerce of any food, drug, device, or cosmetic that is
adulterated or misbranded, and the delivery or proffered delivery thereof for pay or otherwise.
(d) The introduction or delivery for introduction into interstate commerce of any article in
violation of section 404, 505 or 564.
(e) The refusal to permit access to or copying of any record as required by section 412, 414,
416, 504, 564, 703 or 704(a); or the failure to establish or maintain any record, or make any
report, required under section 412, 414(b), 416, 504, 505(i) or (k), 512(a)(4)(C), 512 (j), (l) or
(m), 572(i), 2 515(f), 519, or 564, or the refusal to permit access to or verification or copying of
any such required record.
(f) The refusal to permit entry or inspection as authorized by section 704.
(g) The manufacture, within any Territory of any food, drug, device, or cosmetic that is
adulterated or misbranded.
(h) The giving of a guaranty or undertaking referred to in section 333(c)(2), which guaranty or
undertaking is false, except by a person who relied upon a guaranty or undertaking to the
same effect signed by, containing the name and address of, the person residing in the United
States from whom he received in good faith the food, drug, device, or cosmetic; or the giving of
a guaranty or undertaking referred to in section 333(c)(3), which guaranty or undertaking is
false.
(i) (1) Forging, counterfeiting, simulating, or falsely representing, or without proper authority
using any mark, stamp, tag, label, or other identification device authorized or required by
regulations promulgated under the provisions of section 404, or 721.
(2) Making, selling, disposing of, or keeping in possession, control, or custody, or concealing
any punch, die, plate, stone, or other thing designed to print, imprint, or reproduce the
trademark, trade name, or other identifying mark, imprint, or device of another or any likeness
of any of the foregoing upon any drug or container or labeling thereof so as to render such
drug a counterfeit drug.
(3) The doing of any act which causes a drug to be a counterfeit drug, or the sale or dispensing,
or the holding for sale or dispensing, of a counterfeit drug.
(j) The using by any person to his own advantage, or revealing, other than to the Secretary or
officers or employees of the Department, or to the courts when relevant in any judicial
proceeding under this Act, any information acquired under authority of section 404, 409, 412,
414, 505, 510, 512, 513, 514, 515, 516, 518, 519, 520, 571, 572, 573 , 3 704, 708, or 721
concerning any method or process which as a trade secret is entitled to protection; or the
violating of section 408(i)(2) or any regulation issued under that section. 4 This paragraph
does not authorize the withholding of information from either House of Congress or from, to the
extent of matter within its jurisdiction, any committee or subcommittee of such committee or
any joint committee of Congress or any subcommittee of such joint committee.
(k) The alteration, mutilation, destruction, obliteration, or removal of the whole or any part of
the labeling of, or the doing of any other act with respect to, a food, drug, device, or cosmetic, if
such act is done while such article is held for sale (whether or not the first sale) after shipment
in interstate commerce and results in such article being adulterated or misbranded.
(l) [Deleted] 5
(m) The sale or offering for sale of colored oleomargarine or colored margarine, or the
possession or serving of colored oleomargarine or colored margarine in violation of sections
407(b) or 407(c).
(n) The using, in labeling, advertising or other sales promotion of any reference to any report or
analysis furnished in compliance with section 704.
(o) In the case of a prescription drug distributed or offered for sale in interstate commerce, the
failure of the manufacturer, packer, or distributor thereof to maintain for transmittal, or to
transmit, to any practitioner licensed by applicable State law to administer such drug who
makes written request for information as to such drug, true and correct copies of all printed
matter which is required to be included in any package in which that drug is distributed or sold,
or such other printed matter as is approved by the Secretary. Nothing in this paragraph shall
be construed to exempt any person from any labeling requirement imposed by or under other
provisions of this Act .
(p) The failure to register in accordance with section 510, the failure to provide any information
required by section 510(j) or 510(k), 21 USC § 360(j) or (k)] or the failure to provide a notice
required by section 510(j)(2).
(q)(1) The failure or refusal to (A) comply with any requirement prescribed under section 518
or 520(g), (B) furnish any notification or other material or information required by or under
section 519 or 520(g), or (C) comply with a requirement under section 522.
(2) With respect to any device, the submission of any report that is required by or under this
Act that is false or misleading in any material respect.
(r) The movement of a device in violation of an order under section 304(g) or the removal or
alteration of any mark or label required by the order to identify the device as detained.
(s) The failure to provide the notice required by section 412(c) or 412(e), the failure to make
the reports required by section 412(f)(1)(B), the failure to retain the records required by section
412(b)(4), or the failure to meet the requirements prescribed under section 412(f)(3).
(t) The importation of a drug in violation of section 801(d)(1) , the sale, purchase, or trade of a
drug or drug sample or the offer to sell, purchase, or trade a drug or drug sample in violation of
section 503(c), the sale, purchase, or trade of a coupon, the offer to sell, purchase, or trade
such a coupon, or the counterfeiting of such a coupon in violation of section 503(c)(2), the
distribution of a drug sample in violation of section 503(d) or the failure to otherwise comply
with the requirements of section 503(d), or the distribution of drugs in violation of section 503(e)
or the failure to otherwise comply with the requirements of section 503(e).
(u) The failure to comply with any requirements of the provisions of, or any regulations or
orders of the Secretary, under section 512(a)(4)(A), 512(a)(4)(D), or 512(a)(5).
(v) The introduction or delivery for introduction into interstate commerce of a dietary
supplement that is unsafe under section 413.
(w) The making of a knowingly false statement in any statement, certificate of analysis, record,
or report required or requested under section 801(d)(3); the failure to submit a certificate of
analysis as required under such section; the failure to maintain records or to submit records or
reports as required by such section; the release into interstate commerce of any article or
portion thereof imported into the United States under such section or any finished product
made from such article or portion, except for export in accordance with section 801(e) or 802,
or with section 351(h) of the Public Health Service Act [42 USC § 262(h)]; or the failure to so
export or to destroy such an article or portions thereof, or such a finished product.
(x) The falsification of a declaration of conformity submitted under section 514(c) or the failure
or refusal to provide data or information requested by the Secretary under paragraph (3) of
such section.
(y) In the case of a drug, device, or food –
(1) the submission of a report or recommendation by a person accredited under section 523
that is false or misleading in any material respect;
(2) the disclosure by a person accredited under section 523 of confidential commercial
information or any trade secret without the express written consent of the person who
submitted such information or secret to such person; or
(3) the receipt by a person accredited under section 523 of a bribe in any form or the doing of
any corrupt act by such person associated with a responsibility delegated to such person
under this Act.
(z) [Caution: This subsection terminated Sept. 30, 2006, pursuant to § 401(e) of Act Nov.
21, 1997, P.L. 105-115.] 6 The dissemination of information in violation of section 551.
( aa) The importation of a prescription drug in violation of section 804, the falsification of any
record required to be maintained or provided to the Secretary under section, or any other
violation of regulations under such section.
(bb) The transfer of an article of food in violation of an order under section 304(h), or the
removal or alteration of any mark or label required by the order to identify the article as
detained.
(cc) The importing or offering for import into the United States of an article of food by, with the
assistance of, or at the direction of, a person debarred under section 306(b)(3).
( dd) The failure to register in accordance with section 415.
( ee) The importing or offering for import into the United States of an article of food in violation
of the requirements under section 801(m).
(ff) The importing or offering for import into the United States of a drug or device with respect to
which there is a failure to comply with a request of the Secretary to submit to the Secretary a
statement under section 801(o).
(gg) The knowing failure to comply with paragraph (7)(E) of section 704(g); the knowing
inclusion by a person accredited under paragraph (2) of such section of false information in an
inspection report under paragraph (7)(A) of such section; or the knowing failure of such a
person to include material facts in such a report.
(hh) The failure by a shipper, carrier by motor vehicle or rail vehicle, receiver, or any other
person engaged in the transportation of food to comply with the sanitary transportation
practices prescribed by the Secretary under section 416.
(ii) [Caution: This subsection is effective 1 year after enactment, pursuant to § 4(b) of
Act Dec. 22, 2006, P.L. 109-462.] The falsification of a report of a serious adverse event
submitted to a responsible person (as defined under section 760 or 761) or the falsification of a
serious adverse event report (as defined under section 760 or 761) submitted to the Secretary.
INJUNCTION PROCEEDINGS
SEC. 302 [21 U.S.C. 332] (a) The district courts of the United States and the United States
courts of the Territories shall have jurisdiction, for cause shown 7 to restrain violations of
section 301, except paragraphs (h), (i), and (j).
(b) In case of violation of an injunction or restraining order issued under this section, which
also constitutes a violation of this Act, trial shall be by the court, or, upon demand of the
accused, by a jury.
PENALTIES
SEC. 303. [21 U.S.C. 333] (a)(1) Any person who violates a provision of section 301 shall be
imprisoned for not more than one year or fined not more than $1,000, or both.
(2) Notwithstanding the provisions of paragraph (1) of this section, if any person commits such
a violation after a conviction of him under this section has become final, or commits such a
violation with the intent to defraud or mislead, such person shall be imprisoned for not more
than three years or fined not more than $10,000 or both.
(b)(1) Notwithstanding subsection (a), any person who violates section 301(t) by—
(A) knowingly importing a drug in violation of section 801(d)(1),
(B) knowingly selling, purchasing, or trading a drug or drug sample or knowingly offering to sell,
purchase, or trade a drug or drug sample, in violation of section 503(c)(1),
(C) knowingly selling, purchasing, or trading a coupon, knowingly offering to sell, purchase, or
trade such a coupon, or knowingly counterfeiting such a coupon, in violation of section
503(c)(2), or
(D) knowingly distributing drugs in violation of section 503(e)(2)(A), shall be imprisoned for not
more than 10 years or fined not more than $250,000, or both.
(2) Any manufacturer or distributor who distributes drug samples by means other than the mail
or common carrier whose representative, during the course of the representative’s
employment or association with that manufacturer or distributor, violated section 301(t)
because of a violation of section 503(c)(1) or violated any State law prohibiting the sale,
purchase, or trade of a drug sample subject to section 503(b) or the offer to sell, purchase, or
trade such a drug sample shall, upon conviction of the representative for such violation, be
subject to the following civil penalties:
(A) A civil penalty of not more than $50,000 for each of the first two such violations resulting in
a conviction of any representative of the manufacturer or distributor in any 10-year period.
(B) A civil penalty of not more than $1,000,000 for each violation resulting in a conviction of
any representative after the second conviction in any 10-year period.
For the purposes of this paragraph, multiple convictions of one or more persons arising out of
the same event or transaction, or a related series of events or transactions, shall be
considered as one violation.
(3) Any manufacturer or distributor who violates section 301(t) because of a failure to make a
report required by section 503(d)(3)(E) shall be subject to a civil penalty of not more than
$100,000.
(4)(A) If a manufacturer or distributor or any representative of such manufacturer or distributor
provides information leading to the institution of a criminal proceeding against, and conviction
of, any representative of that manufacturer or distributor for a violation of section 301(t)
because of a sale, purchase, or trade or offer to purchase, sell, or trade a drug sample in
violation of section 503(c)(1) or for a violation of State law prohibiting the sale, purchase, or
trade or offer to sell, purchase, or trade a drug sample, the conviction of such representative
shall not be considered as a violation for purposes of paragraph (2).
(B) If, in an action brought under paragraph (2) against a manufacturer or distributor relating to
the conviction of a representative of such manufacturer or distributor for the sale, purchase, or
trade of a drug or the offer to sell, purchase, or trade a drug, it is shown, by clear and
convincing evidence—
(i) that the manufacturer or distributor conducted, before the institution of a criminal proceeding
against such representative for the violation which resulted in such conviction, an investigation
of events or transactions which would have led to the reporting of information leading to the
institution of a criminal proceeding against, and conviction of, such representative for such
purchase, sale, or trade or offer to purchase, sell, or trade, or
(ii) that, except in the case of the conviction of a representative employed in a supervisory
function, despite diligent implementation by the manufacturer or distributor of an independent
audit and security system designed to detect such a violation, the manufacturer or distributor
could not reasonably have been expected to have detected such violation, the conviction of
such representative shall not be considered as a conviction for purposes of paragraph (2).
(5) If a person provides information leading to the institution of a criminal proceeding against,
and conviction of, a person for a violation of section 301(t) because of the sale, purchase, or
trade of a drug sample or the offer to sell, purchase, or trade a drug sample in violation of
section 503(c)(1), such person shall be entitled to one-half of the criminal fine imposed and
collected for such violation but not more than $125,000.
(6) Notwithstanding subsection (a), any person who is a manufacturer or importer of a
prescription drug under section 804(b) and knowingly fails to comply with a requirement of
section 804(e) that is applicable to such manufacturer or importer, respectively, shall be
imprisoned for not more than 10 years or fined not more than $250,000, or both.
(c) No person shall be subject to the penalties of subsection (a)(1) of this section, (1) for
having received in interstate commerce any article and delivered it or proffered delivery of it, if
such delivery or proffer was made in good faith, unless he refuses to furnish on request of an
officer or employee duly designated by the Secretary the name and address of the person
from whom he purchased or received such article and copies of all documents, if any there be,
pertaining to the delivery of the article to him; or (2) for having violated section 301(a) or (d), if
he establishes a guaranty or undertaking signed by, and containing the name and address of,
the person residing in the United States from whom he received in good faith the article, to the
effect, in case of an alleged violation of section 301(a), that such article is not adulterated or
misbranded, within the meaning of this Act, designating this Act, or to the effect, in case of an
alleged violation of section 301(d), that such article is not an article which may not, under the
provisions of section 404 or 505, be introduced into interstate commerce; or (3) for having
violated section 301(a), where the violation exists because the article is adulterated by reason
of containing a color additive not from a batch certified in accordance with regulations
promulgated by the Secretary under this Act, if such person establishes a guaranty or
undertaking signed by, and containing the name and address of, the manufacturer of the color
additive, to the effect that such color additive was from a batch certified in accordance with the
applicable regulations promulgated by the Secretary under this Act; or (4) for having violated
section 301 (b), (c), or (k) by failure to comply with section 502(f) in respect to an article
received in interstate commerce to which neither section 503(a) nor section 503(b)(1) is
applicable, if the delivery or proffered delivery was made in good faith and the labeling at the
time thereof contained the same directions for use and warning statements as were contained
in the labeling at the time of such receipt of such article; or (5) for having violated section
301(i)(2) if such person acted in good faith and had no reason to believe that use of the punch,
die, plate, stone, or other thing involved would result in a drug being a counterfeit drug, or for
having violated section 301(i)(3) if the person doing the act or causing it to be done acted in
good faith and had no reason to believe that the drug was a counterfeit drug.
(d) No person shall be subject to the penalties of subsection (a)(1) of this section for a violation
of section 301 involving misbranded food if the violation exists solely because the food is
misbranded under section 403(a)(2) because of its advertising.
(e)(1) Except as provided in paragraph (2), whoever knowingly distributes, or possesses with
intent to distribute, human growth hormone for any use in humans other than the treatment of
a disease or other recognized medical condition, where such use has been authorized by the
Secretary of Health and Human Services under section 505 and pursuant to the order of a
physician, is guilty of an offense punishable by not more than 5 years in prison, such fines as
are authorized by title 18, United States Code, or both.
(2) Whoever commits any offense set forth in paragraph (1) and such offense involves an
individual under 18 years of age is punishable by not more than 10 years imprisonment, such
fines as are authorized by title 18, United States Code, or both.
(3) Any conviction for a violation of paragraphs (1) and (2) of this subsection shall be
considered a felony violation of the Controlled Substances Act for the purposes of forfeiture
under section 413 of such Act.
(4) As used in this subsection the term ‘‘human growth hormone’’ means somatrem,
somatropin, or an analogue of either of them.
(5) The Drug Enforcement Administration is authorized to investigate offenses punishable by
this subsection.
(f)(1) (A) 8 Except as provided in subparagraph (B), any person who violates a requirement of
this Act which relates to devices shall be liable to the United States for a civil penalty in an
amount not to exceed $15,000 for each such violation, and not to exceed $1,000,000 for all
such violations adjudicated in a single proceeding. For purposes of the preceding sentence, a
person accredited under paragraph (2) of section 704(g) who is substantially not in compliance
with the standards of accreditation under such section, or who poses a threat to public health
or fails to act in a manner that is consistent with the purposes of such section, shall be
considered to have violated a requirement of this Act that relates to devices.
(B) Subparagraph (A) shall not apply—
(i) to any person who violates the requirements of section 519(a) or 520(f) unless such
violation constitutes (I) a significant or knowing departure from such requirements, or (II) a risk
to public health,
(ii) to any person who commits minor violations of section 519(e) or 519(f) (only with respect to
correction reports) if such person demonstrates substantial compliance with such section, or
(iii) to violations of section 501(a)(2)(A) which involve one or more devices which are not
defective.
(2)(A) Any person who introduces into interstate commerce or delivers for introduction into
interstate commerce an article of food that is adulterated within the meaning of section
402(a)(2)(B) shall be subject to a civil money penalty of not more than $50,000 in the case of
an individual and $250,000 in the case of any other person for such introduction or delivery,
not to exceed $500,000 for all such violations adjudicated in a single proceeding.
(B) This paragraph shall not apply to any person who grew the article of food that is
adulterated. If the Secretary assesses a civil penalty against any person under this paragraph,
the Secretary may not use the criminal authorities under this section to sanction such person
for the introduction or delivery for introduction into interstate commerce of the article of food
that is adulterated. If the Secretary assesses a civil penalty against any person under this
paragraph, the Secretary may not use the seizure authorities of section 304 or the injunction
authorities of section 302 with respect to the article of food that is adulterated.
(C) In a hearing to assess a civil penalty under this paragraph, the presiding officer shall have
the same authority with regard to compelling testimony or production of documents as a
presiding officer has under section 408(g)(2)(B). The third sentence of paragraph (3)(A) shall
not apply to any investigation under this paragraph.
(3)(A) A civil penalty under paragraph (1) or (2) shall be assessed by the Secretary by an order
made on the record after opportunity for a hearing provided in accordance with this
subparagraph and section 554 of title 5, United States Code. Before issuing such an order, the
Secretary shall give written notice to the person to be assessed a civil penalty under such
order of the Secretary’s proposal to issue such order and provide such person an opportunity
for a hearing on the order. In the course of any investigation, the Secretary may issue
subpoenas requiring the attendance and testimony of witnesses and the production of
evidence that relates to the matter under investigation.
(B) In determining the amount of a civil penalty, the Secretary shall take into account the
nature, circumstances, extent, and gravity of the violation or violations and, with respect to the
violator, ability to pay, effect on ability to continue to do business, any history of prior such
violations, the degree of culpability, and such other matters as justice may require.
(C) The Secretary may compromise, modify, or remit, with or without conditions, any civil
penalty which may be assessed under paragraph (1) or (2). The amount of such penalty, when
finally determined, or the amount agreed upon in compromise, may be deducted from any
sums owing by the United States to the person charged.
(4) Any person who requested, in accordance with paragraph (3)(A), a hearing respecting the
assessment of a civil penalty and who is aggrieved by an order assessing a civil penalty may
file a petition for judicial review of such order with the United States Court of Appeals for the
District of Columbia Circuit or for any other circuit in which such person resides or transacts
business. Such a petition may only be filed within the 60-day period beginning on the date the
order making such assessment was issued.
(5) If any person fails to pay an assessment of a civil penalty—
(A) after the order making the assessment becomes final, and if such person does not file a
petition for judicial review of the order in accordance with paragraph (4), or
(B) after a court in an action brought under paragraph (4) has entered a final judgment in favor
of the Secretary, the Attorney General shall recover the amount assessed (plus interest at
currently prevailing rates from the date of the expiration of the 60-day period referred to in
paragraph (4) or the date of such final judgment, as the case may be) in an action brought in
any appropriate district court of the United States. In such an action, the validity, amount, and
appropriateness of such penalty shall not be subject to review.
SEIZURE
SEC. 304. [21 U.S.C. 334] (a) (1) Any article of food, drug, or cosmetic that is adulterated or
misbranded when introduced into or while in interstate commerce or while held for sale
(whether or not the first sale) after shipment in interstate commerce, or which may not, under
the provisions of section 404 or 505, be introduced into interstate commerce, shall be liable to
be proceeded against while in interstate commerce, or at any time thereafter, on libel of
information and condemned in any district court of the United States or United States court of a
Territory within the jurisdiction of which the article is found. No libel for condemnation shall be
instituted under this Act, for any alleged misbranding if there is pending in any court a libel for
condemnation proceeding under this Act based upon the same alleged misbranding, and not
more than one such proceeding shall be instituted if no such proceeding is so pending, except
that such limitations shall not apply (A) when such misbranding has been the basis of a prior
judgment in favor of the United States, in a criminal, injunction, or libel for condemnation
proceeding under this Act, or (B) when the Secretary has probable cause to believe from facts
found, without hearing, by him or any officer or employee of the Department that the
misbranded article is dangerous to health, or that the labeling of the misbranded article is
fraudulent, or would be in a material respect misleading to the injury or damage of the
purchaser or consumer. In any case where the number of libel for condemnation proceedings
is limited as above provided the proceeding pending or instituted shall, on application of the
claimant, seasonably made, be removed for trial to any district agreed upon by stipulation
between the parties, or, in case of failure to so stipulate within a reasonable time, the claimant
may apply to the court of the district in which the seizure has been made, and such court (after
giving the United States attorney for such district reasonable notice and opportunity to be
heard) shall by order, unless good cause to the contrary is shown, specify a district of
reasonable proximity to the claimant's principal place of business, to which the case shall be
removed for trial.
(2) The following shall be liable to be proceeded against at any time on libel of information and
condemned in any district court of the United States or United States court of a Territory within
the jurisdiction of which they are found: (A) Any drug that is a counterfeit drug, (B) Any
container of a counterfeit drug, (C) Any punch, die, plate, stone, labeling, container, or other
thing used or designed for use in making a counterfeit drug or drugs, and (D) Any adulterated
or misbranded device.
(3) (A) Except as provided in subparagraph (B), no libel for condemnation may be instituted
under paragraph (1) or (2) against any food which -
(i) is misbranded under section 403(a)(2) because of its advertising, and
(ii) is being held for sale to the ultimate consumer in an establishment other than an
establishment owned or operated by a manufacturer, packer, or distributor of the food.
(B) A libel for condemnation may be instituted under paragraph (1) or (2) against a food
described in subparagraph (A) if –
(i)(I) the food's advertising which resulted in the food being misbranded under section 403(a)(2)
was disseminated in the establishment in which the food is being held for sale to the ultimate
consumer,
(II) such advertising was disseminated by, or under the direction of, the owner or operator of
such establishment, or
(III) all or part of the cost of such advertising was paid by such owner or operator; and
(ii) the owner or operator of such establishment used such advertising in the establishment to
promote the sale of the food.
(b) The article, equipment, or other thing proceeded against shall be liable to seizure by
process pursuant to the libel, and the procedure in cases under this section shall conform, as
nearly as may be, to the procedure in admiralty; except that on demand of either party any
issue of fact joined in any such case shall be tried by jury. When libel for condemnation
proceedings under this section, involving the same claimant and the same issues of
adulteration or misbranding, are pending in two or more jurisdictions, such pending
proceedings, upon application of the claimant seasonably made to the court of one such
jurisdiction, shall be consolidated for trial by order of such court, and tried in (1) any district
selected by the claimant where one of such proceedings is pending; or (2) a district agreed
upon by stipulation between the parties. If no order for consolidation is so made within a
reasonable time, the claimant may apply to the court of one such jurisdiction and such court
(after giving the United States attorney for such district reasonable notice and opportunity to be
heard) shall by order, unless good cause to the contrary is shown, specify a district of
reasonable proximity to the claimant's principal place of business, in which all such pending
proceedings shall be consolidated for trial and tried. Such order of consolidation shall not apply
so as to require the removal of any case the date for trial of which has been fixed. The court
granting such order shall give prompt notification thereof to the other courts having jurisdiction
of the cases covered thereby.
(c) The court at any time after seizure up to a reasonable time before trial shall by order allow
any party to a condemnation proceeding, his attorney or agent, to obtain a representative
sample of the article seized and a true copy of the analysis, if any, on which the proceeding is
based and the identifying marks or numbers, if any, of the packages from which the samples
analyzed were obtained.
(d)(1) Any food, drug, device, or cosmetic condemned under this section shall, after entry of
the decree, be disposed of by destruction or sale as the court may, in accordance with the
provisions of this section, direct and the proceeds thereof, if sold, less the legal costs and
charges, shall be paid into the Treasury of the United States; but such article shall not be sold
under such decree contrary to the provisions of this Act or the laws of the jurisdiction in which
sold. After entry of the decree and upon the payment of the costs of such proceedings and the
execution of a good and sufficient bond conditioned that such article shall not be sold or
disposed of contrary to the provisions of this Act or the laws of any State or Territory in which
sold, the court may by order direct that such article be delivered to the owner thereof to be
destroyed or brought into compliance with the provisions of this Act, under the supervision of
an officer or employee duly designated by the Secretary, and the expenses of such
supervision shall be paid by the person obtaining release of the article under bond. If the article
was imported into the United States and the person seeking its release establishes (A) that the
adulteration, misbranding, or violation did not occur after the article was imported, and (B) that
he had no cause for believing that it was adulterated, misbranded, or in violation before it was
released from customs custody, the court may permit the article to be delivered to the owner
for exportation in lieu of destruction upon a showing by the owner that all of the conditions of
section 801(e) can and will be met. The provisions of this sentence shall not apply where
condemnation is based upon violation of section 402(a)(1), (2), or (6), section 501(a)(3),
section 502(j), or section 601(a) or (d). Where such exportation is made to the original foreign
supplier, then paragraphs (1) and (2) of section 801(e) and the preceding sentence shall not
be applicable; and in all cases of exportation the bond shall be conditioned that the article shall
not be sold or disposed of until the applicable conditions of section 801(e) have been met. Any
article condemned by reason of its being an article which may not, under section 404 or 505,
be introduced into interstate commerce, shall be disposed of by destruction.
(2) The provisions of paragraph (1) of this subsection shall, to the extent deemed appropriate
by the court, apply to any equipment or other thing which is not otherwise within the scope of
such paragraph and which is referred to in paragraph (2) of subsection (a).
(3) Whenever in any proceeding under this section, involving paragraph (2) of subsection (a),
the condemnation of any equipment or thing (other than a drug) is decreed, the court shall
allow the claim of any claimant, to the extent of such claimant's interest, for remission or
mitigation of such forfeiture if such claimant proves to the satisfaction of the court (i) that he
has not committed or caused to be committed any prohibited act referred to in such paragraph
(2) and has no interest in any drug referred to therein, (ii) that he has an interest in such
equipment or other thing as owner or lienor or otherwise, acquired by him in good faith, and (iii)
that he at no time had any knowledge or reason to believe that such equipment or other thing
was being or would be used in, or to facilitate, the violation of laws of the United States relating
to counterfeit drugs.
(e) When a decree of condemnation is entered against the article, court costs and fees, and
storage and other proper expenses, shall be awarded against the person, if any, intervening as
claimant of the article.
(f) In the case of removal for trial of any case as provided by subsection (a) or (b) -
(1) The clerk of the court from which removal is made shall promptly transmit to the court in
which the case is to be tried all records in the case necessary in order that such court may
exercise jurisdiction.
(2) The court to which such case was removed shall have the powers and be subject to the
duties, for purposes of such case, which the court from which removal was made would have
had, or to which such court would have been subject, if such case had not been removed.
(g)(1) If during an inspection conducted under section 704 of a facility or a vehicle, a device
which the officer or employee making the inspection has reason to believe is adulterated or
misbranded is found in such facility or vehicle, such officer or employee may order the device
detained (in accordance with regulations prescribed by the Secretary) for a reasonable period
which may not exceed twenty days unless the Secretary determines that a period of detention
greater than twenty days is required to institute an action under subsection (a) or section 302,
in which case he may authorize a detention period of not to exceed thirty days. Regulations of
the Secretary prescribed under this paragraph shall require that before a device may be
ordered detained under this paragraph the Secretary or an officer or employee designated by
the Secretary approve such order. A detention order under this paragraph may require the
labeling or marking of a device during the period of its detention for the purpose of identifying
the device as detained. Any person who would be entitled to claim a device if it were seized
under subsection (a) may appeal to the Secretary a detention of such device under this
paragraph. Within five days of the date an appeal of a detention is filed with the Secretary, the
Secretary shall after affording opportunity for an informal hearing by order confirm the
detention or revoke it.
(2)(A) Except as authorized by subparagraph (B), a device subject to a detention order issued
under paragraph (1) shall not be moved by any person from the place at which it is ordered
detained until –
(i) released by the Secretary, or
(ii) the expiration of the detention period applicable to such order, whichever occurs first.
(B) A device subject to a detention order under paragraph (1) may be moved –
(i) in accordance with regulations prescribed by the Secretary, and
(ii) if not in final form for shipment, at the discretion of the manufacturer of the device for the
purpose of completing the work required to put it in such form.
(h) Administrative Detention of Foods.—
(1) Detention authority.--
(A) In general.--An officer or qualified employee of the Food and Drug Administration may
order the detention, in accordance with this subsection, of any article of food that is found
during an inspection, examination, or investigation under this Act conducted by such officer or
qualified employee, if the officer or qualified employee has credible evidence or information
indicating that such article presents a threat of serious adverse health consequences or death
to humans or animals.
(B) Secretary's approval.--An article of food may be ordered detained under subparagraph (A)
only if the Secretary or an official designated by the Secretary approves the order. An official
may not be so designated unless the official is the director of the district under this Act in which
the article involved is located, or is an official senior to such director.
(2) Period of detention.--An article of food may be detained under paragraph (1) for a
reasonable period, not to exceed 20 days, unless a greater period, not to exceed 30 days, is
necessary, to enable the Secretary to institute an action under subsection (a) or section
302. The Secretary shall by regulation provide for procedures for instituting such action on an
expedited basis with respect to perishable foods.
(3) Security of detained article.--An order under paragraph (1) with respect to an article of food
may require that such article be labeled or marked as detained, and shall require that the
article be removed to a secure facility, as appropriate. An article subject to such an order shall
not be transferred by any person from the place at which the article is ordered detained, or
from the place to which the article is so removed, as the case may be, until released by the
Secretary or until the expiration of the detention period applicable under such order, whichever
occurs first. This subsection may not be construed as authorizing the delivery of the article
pursuant to the execution of a bond while the article is subject to the order, and section 801(b)
does not authorize the delivery of the article pursuant to the execution of a bond while the
article is subject to the order.
(4) Appeal of detention order.--
(A) In general.--With respect to an article of food ordered detained under paragraph (1), any
person who would be entitled to be a claimant for such article if the article were seized under
subsection (a) may appeal the order to the Secretary. Within five days after such an appeal is
filed, the Secretary, after providing opportunity for an informal hearing, shall confirm or
terminate the order involved, and such confirmation by the Secretary shall be considered a
final agency action for purposes of section 702 of title 5, United States Code. If during such
five-day period the Secretary fails to provide such an opportunity, or to confirm or terminate
such order, the order is deemed to be terminated.
(B) Effect of instituting court action.— The process under subparagraph (A) for the appeal of
an order under paragraph (1) terminates if the Secretary institutes an action under subsection
(a) or section 302 regarding the article of food involved.
HEARING BEFORE REPORT OF CRIMINAL VIOLATION
SEC. 305. [21 U.S.C. 335] Before any violation of this Act is reported by the Secretary to any
United States attorney for institution of a criminal proceeding, the person against whom such
proceeding is contemplated shall be given appropriate notice and an opportunity to present his
views, either orally or in writing, with regard to such contemplated proceeding.
DEBARMENT, TEMPORARY DENIAL OF APPROVAL, AND SUSPENSION
SEC. 306. [ 21 U.S.C. 335a] (a) MANDATORY DEBARMENT; CERTAIN DRUG
APPLICATIONS. –
(1) CORPORATIONS, PARTNERSHIPS, AND ASSOCIATIONS. -- If the Secretary finds that
a person other than an individual has been convicted, after the date of enactment of this
section, of a felony under Federal law for conduct relating to the development or approval,
including the process for development or approval, of any abbreviated drug application, the
Secretary shall debar such person from submitting, or assisting in the submission of, any such
application.
(2) INDIVIDUALS. -- If the Secretary finds that an individual has been convicted of a felony
under Federal law for conduct –
(A) relating to the development or approval, including the process for development or approval,
of any drug product, or
(B) otherwise relating to the regulation of any drug product under this Act, the Secretary shall
debar such individual from providing services in any capacity to a person that has an approved
or pending drug product application.
(b) Permissive Debarment; Certain Drug Applications; Food Imports.—
(1) IN GENERAL. -- The Secretary, on the Secretary's own initiative or in response to a
petition, may, in accordance with paragraph (2), debar –
(A) a person other than an individual from submitting or assisting in the submission of any
abbreviated drug application, or
(B) an individual from providing services in any capacity to a person that has an approved or
pending drug product application . , or
(C) a person from importing an article of food or offering such an article for import into the
United States .
(2) PERSONS SUBJECT TO Permissive debarment; certain drug applications. -- The
following persons are subject to debarment under subparagraph (A) or (B) of paragraph (1):
(A) CORPORATIONS, PARTNERSHIPS, AND ASSOCIATIONS. -- Any person other than an
individual that the Secretary finds has been convicted –
(i) for conduct that –
(I) relates to the development or approval, including the process for the development or
approval, of any abbreviated drug application; and
(II) is a felony under Federal law (if the person was convicted before the date of enactment of
this section), a misdemeanor under Federal law, or a felony under State law, or
(ii) of a conspiracy to commit, or aiding or abetting, a criminal offense described in clause (i) or
a felony described in subsection (a)(1),
if the Secretary finds that the type of conduct which served as the basis for such conviction
undermines the process for the regulation of drugs.
(B) INDIVIDUALS. –
(i) Any individual whom the Secretary finds has been convicted of –
(I) a misdemeanor under Federal law or a felony under State law for conduct relating to the
development or approval, including the process for development or approval, of any drug
product or otherwise relating to the regulation of drug products under this Act, or
(II) a conspiracy to commit, or aiding or abetting, such criminal offense or a felony described in
subsection (a)(2),
if the Secretary finds that the type of conduct which served as the basis for such conviction
undermines the process for the regulation of drugs.
(ii) Any individual whom the Secretary finds has been convicted of –
(I) a felony which is not described in subsection (a)(2) or clause (i) of this subparagraph and
which involves bribery, payment of illegal gratuities, fraud, perjury, false statement,
racketeering, blackmail, extortion, falsification or destruction of records, or interference with,
obstruction of an investigation into, or prosecution of, any criminal offense, or
(II) a conspiracy to commit, or aiding or abetting, such felony,
If the Secretary finds, on the basis of the conviction of such individual and other information,
that such individual has demonstrated a pattern of conduct sufficient to find that there is
reason to believe that such individual may violate requirements under this Act relating to drug
products.
(iii) Any individual whom the Secretary finds materially participated in acts that were the basis
for a conviction for an offense described in subsection (a) or in clause (i) or (ii) for which a
conviction was obtained, if the Secretary finds, on the basis of such participation and other
information, that such individual has demonstrated a pattern of conduct sufficient to find that
there is reason to believe that such individual may violate requirements under this Act relating
to drug products.
(iv) Any high managerial agent whom the Secretary finds –
(I) worked for, or worked as a consultant for, the same person as another individual during the
period in which such other individual took actions for which a felony conviction was obtained
and which resulted in the debarment under subsection (a)(2), or clause (i), of such other
individual,
(II) had actual knowledge of the actions described in subclause (I) of such other individual, or
took action to avoid such actual knowledge, or failed to take action for the purpose of avoiding
such actual knowledge,
(III) knew that the actions described in subclause (I) were violative of law, and
(IV) did not report such actions, or did not cause such actions to be reported, to an officer,
employee, or agent of the Department or to an appropriate law enforcement officer, or failed to
take other appropriate action that would have ensured that the process for the regulation of
drugs was not undermined, within a reasonable time after such agent first knew of such
actions,
if the Secretary finds that the type of conduct which served as the basis for such other
individual's conviction undermines the process for the regulation of drugs.
(3) Persons subject to permissive debarment; food importation.--A person is subject to
debarment under paragraph (1)(C) if--
(A) the person has been convicted of a felony for conduct relating to the importation into the
United States of any food; or
(B) the person has engaged in a pattern of importing or offering for import adulterated food that
presents a threat of serious adverse health consequences or death to humans or animals.
(4) STAY OF CERTAIN ORDERS. An order of the Secretary under clause (iii) or (iv) of
paragraph (2)(B) shall not take effect until 30 days after the order has been issued.
(c) DEBARMENT PERIODS AND CONSIDERATIONS. --
(1) EFFECT OF DEBARMENT. -- The Secretary -
(A) shall not accept or review (other than in connection with an audit under this section) any
abbreviated drug application submitted by or with the assistance of a person debarred under
subsection (a)(1) or (b)(2)(A) during the period such person is debarred,
(B) shall, during the period of a debarment under subsection (a)(2) or (b)(2)(B), debar an
individual from providing services in any capacity to a person that has an approved or pending
drug product application and shall not accept or review (other than in connection with an audit
under this section) an abbreviated drug application from such individual, and
(C) shall, if the Secretary makes the finding described in paragraph (6) or (7) of section 307(a),
assess a civil penalty in accordance with section 307.
(2) DEBARMENT PERIODS. --
(A) IN GENERAL. -- The Secretary shall debar a person under subsection (a) or (b) for the
following periods:
(i) The period of debarment of a person (other than an individual) under subsection (a)(1) shall
not be less than 1 year or more than 10 years, but if an act leading to a subsequent debarment
under subsection (a) occurs within 10 years after such person has been debarred under
subsection (a)(1), the period of debarment shall be permanent.
(ii) The debarment of an individual under subsection (a)(2) shall be permanent.
(iii) The period of debarment of any person under paragraph (2) or (3) of subsection (b) shall
not be more than 5 years. The Secretary may determine whether debarment periods shall run
concurrently or consecutively in the case of a person debarred for multiple offenses.
(B) NOTIFICATION. -- Upon a conviction for an offense described in subsection (a) or (b) or
upon execution of an agreement with the United States to plead guilty to such an offense, the
person involved may notify the Secretary that the person acquiesces to debarment and such
person's debarment shall commence upon such notification.
(3) CONSIDERATIONS. -- In determining the appropriateness and the period of a debarment
of a person under subsection (b) and any period of debarment beyond the minimum specified
in subparagraph (A)(i) of paragraph (2), the Secretary shall consider where applicable -
(A) the nature and seriousness of any offense involved,
(B) the nature and extent of management participation in any offense involved, whether
corporate policies and practices encouraged the offense, including whether inadequate
institutional controls contributed to the offense,
(C) the nature and extent of voluntary steps to mitigate the impact on the public of any offense
involved, including the recall or the discontinuation of the distribution of suspect drugs, full
cooperation with any investigations (including the extent of disclosure to appropriate
authorities of all wrongdoing), the relinquishing of profits on drug approvals fraudulently
obtained, and any other actions taken to substantially limit potential or actual adverse effects
on the public health,
(D) whether the extent to which changes in ownership, management, or operations have
corrected the causes of any offense involved and provide reasonable assurances that the
offense will not occur in the future,
(E) whether the person to be debarred is able to present adequate evidence that current
production of drugs subject to abbreviated drug applications and all pending abbreviated drug
applications are free of fraud or material false statements, and
(F) prior convictions under this Act or under other Acts involving matters within the jurisdiction
of the Food and Drug Administration.
(d) TERMINATION OF DEBARMENT. --
(1) APPLICATION. -- Any person that is debarred under subsection (a) (other than a person
permanently debarred) or any person that is debarred under subsection (b) of this section may
apply to the Secretary for termination of the debarment under this subsection. Any information
submitted to the Secretary under this paragraph does not constitute an amendment or
supplement to pending or approved abbreviated drug applications.
(2) DEADLINE. -- The Secretary shall grant or deny any application respecting a debarment
which is submitted under paragraph (1) within 180 days of the date the application is
submitted.
(3) ACTION BY THE SECRETARY. –
(A) CORPORATIONS. --
(i) CONVICTION REVERSAL. -- If the conviction which served as the basis for the debarment
of a person under subsection (a)(1) (b) or paragraph (2)(A) or (3) of subsection is reversed, the
Secretary shall withdraw the order of debarment.
(ii) APPLICATION. -- Upon application submitted under paragraph (1), the Secretary shall
terminate the debarment of a person if the Secretary finds that –
(I) changes in ownership, management, or operations have fully corrected the causes of the
offense involved and provide reasonable assurances that the offense will not occur in the
future, and
(II) in applicable cases, sufficient audits, conducted by the Food and Drug Administration or by
independent experts acceptable to the Food and Drug Administration, demonstrate that
pending applications and the development of drugs being tested before the submission of an
application are free of fraud or material false statements.
In the case of persons debarred under subsection (a)(1), such termination shall take effect no
earlier than the expiration of one year from the date of the debarment.
(B) INDIVIDUALS. –
(i) CONVICTION REVERSAL. -- If the conviction which served as the basis for the debarment
of an individual under subsection (a)(2) or clause (i), (ii), (iii), or (iv) of subsection (b)(2)(B) or
subsection (b)(3) is reversed, the Secretary shall withdraw the order of debarment.
(ii) APPLICATION. -- Upon application submitted under paragraph (1), the Secretary shall
terminate the debarment of an individual who has been debarred under subsection (b)(2)(B) or
subsection (b)(3) if such termination serves the interests of justice and adequately protects the
integrity of the drug approval process or the food importation process, as the case may be.
(4) SPECIAL TERMINATION. –
(A) APPLICATION. -- Any person that is debarred under subsection (a)(1) (other than a person
permanently debarred under subsection (c)(2)(A)(i)) or any individual who is debarred under
subsection (a)(2) may apply to the Secretary for special termination of debarment under this
subsection. Any information submitted to the Secretary under this subparagraph does not
constitute an amendment or supplement to pending or approved abbreviated drug
applications.
(B) CORPORATIONS. -- Upon an application submitted under subparagraph (A), the
Secretary may take the action described in subparagraph (D) if the Secretary, after an informal
hearing, finds that –
(i) the person making the application under subparagraph (A) has demonstrated that the felony
conviction which was the basis for such person's debarment involved the commission of an
offense which was not authorized, requested, commanded, performed, or recklessly tolerated
by the board of directors or by a high managerial agent acting on behalf of the person within
the scope of the board's or agent's office or employment,
(ii) all individuals who were involved in the commission of the offense or who knew or should
have known of the offense have been removed from employment involving the development or
approval of any drug subject to sections 9 505,
(iii) the person fully cooperated with all investigations and promptly disclosed all wrongdoing to
the appropriate authorities, and
(iv) the person acted to mitigate any impact on the public of any offense involved, including the
recall, or the discontinuation of the distribution, of any drug with respect to which the Secretary
requested a recall or discontinuation of distribution due to concerns about the safety or efficacy
of the drug.
(C) INDIVIDUALS. -- Upon an application submitted under subparagraph (A), the Secretary
may take the action described in subparagraph (D) if the Secretary, after an informal hearing,
finds that such individual has provided substantial assistance in the investigations or
prosecutions of offenses which are described in subsection (a) or (b) or which relate to any
matter under the jurisdiction of the Food and Drug Administration.
(D) SECRETARIAL ACTION -- The action referred to in subparagraphs (B) and (C) is –
(i) in the case of a person other than an individual –
(I) terminating the debarment immediately, or
(II) limiting the period of debarment to less than one year, and
(ii) in the case of an individual, limiting the period of debarment to less than permanent but to
no less than 1 year, whichever best serves the interest of justice and protects the integrity of
the drug approval process.
(e) PUBLICATION AND LIST OF DEBARRED PERSONS. -- The Secretary shall publish in
the Federal Register the name of any person debarred under subsection (a) or (b), the
effective date of the debarment, and the period of the debarment. The Secretary shall also
maintain and make available to the public a list, updated no less often than quarterly, of such
persons, of the effective dates and minimum periods of such debarments, and of the
termination of debarments.
(f) TEMPORARY DENIAL OF APPROVAL. --
(1) IN GENERAL. -- The Secretary, on the Secretary's own initiative or in response to a
petition, may, in accordance with paragraph (3), refuse by order, for the period prescribed by
paragraph (2), to approve any abbreviated drug application submitted by any person –
(A) if such person is under an active Federal criminal investigation in connection with an action
described in subparagraph (B),
(B) if the Secretary finds that such person –
(i) has bribed or attempted to bribe, has paid or attempted to pay an illegal gratuity, or has
induced or attempted to induce another person to bribe or pay an illegal gratuity to any officer,
employee, or agent of the Department of Health and Human Services or to any other Federal,
State, or local official in connection with any abbreviated drug application, or has conspired to
commit, or aided or abetted, such actions, or
(ii) has knowingly made or caused to be made a pattern or practice of false statements or
misrepresentations with respect to material facts relating to any abbreviated drug application,
or the production of any drug subject to an abbreviated drug application, to any officer,
employee, or agent of the Department of Health and Human Services, or has conspired to
commit, or aided or abetted, such actions, and
(C) if a significant question has been raised regarding –
(i) the integrity of the approval process with respect to such abbreviated drug application, or
(ii) the reliability of data in or concerning such person's abbreviated drug application.
Such an order may be modified or terminated at any time.
(2) APPLICABLE PERIOD. --
(A) IN GENERAL. -- Except as provided in subparagraph (B), a denial of approval of an
application of a person under paragraph (1) shall be in effect for a period determined by the
Secretary but not to exceed 18 months beginning on the date the Secretary finds that the
conditions described in subparagraphs (A), (B), and (C) of paragraph (1) exist. The Secretary
shall terminate such denial -
(i) if the investigation with respect to which the finding was made does not result in a criminal
charge against such person, if criminal charges have been brought and the charges have been
dismissed, or if a judgment of acquittal has been entered, or
(ii) if the Secretary determines that such finding was in error.
(B) EXTENSION. -- If, at the end of the period described in subparagraph (A), the Secretary
determines that a person has been criminally charged for an action described in subparagraph
(B) of paragraph (1), the Secretary may extend the period of denial of approval of an
application for a period not to exceed 18 months. The Secretary shall terminate such extension
if the charges have been dismissed, if a judgment of acquittal has been entered, or if the
Secretary determines that the finding described in subparagraph (A) was in error.
(3) INFORMAL HEARING. -- Within 10 days of the date an order is issued under paragraph (1),
the Secretary shall provide such person with an opportunity for an informal hearing, to be held
within such 10 days, on the decision of the Secretary to refuse approval of an abbreviated drug
application. Within 60 days of the date on which such hearing is held, the Secretary shall notify
the person given such hearing whether the Secretary's refusal of approval will be continued,
terminated, or otherwise modified. Such notification shall be final agency action.
(g) SUSPENSION AUTHORITY. --
(1) IN GENERAL. -- If -
(A) the Secretary finds -
(i) that a person has engaged in conduct described in subparagraph (B) of subsection (f)(1) in
connection with 2 or more drugs under abbreviated drug applications, or
(ii) that a person has engaged in flagrant and repeated, material violations of good
manufacturing practice or good laboratory practice in connection with the development,
manufacturing, or distribution of one or more drugs approved under an abbreviated drug
application during a 2-year period, and -
(I) such violations may undermine the safety and efficacy of such drugs, and
(II) the causes of such violations have not been corrected within a reasonable period of time
following notice of such violations by the Secretary, and
(B) such person is under an active investigation by a Federal authority in connection with a civil
or criminal action involving conduct described in subparagraph (A), the Secretary shall issue
an order suspending the distribution of all drugs the development or approval of which was
related to such conduct described in subparagraph (A) or suspending the distribution of all
drugs approved under abbreviated drug applications of such person if the Secretary finds that
such conduct may have affected the development or approval of a significant number of drugs
which the Secretary is unable to identify. The Secretary shall exclude a drug from such order if
the Secretary determines that such conduct was not likely to have influenced the safety or
efficacy of such drug.
(2) PUBLIC HEALTH WAIVER. -- The Secretary shall, on the Secretary's own initiative or in
response to a petition, waive the suspension under paragraph (1) (involving an action
described in paragraph (1)(A)(i)) with respect to any drug if the Secretary finds that such
waiver is necessary to protect the public health because sufficient quantities of the drug would
not otherwise be available. The Secretary shall act on any petition seeking action under this
paragraph within 180 days of the date the petition is submitted to the Secretary.
(h) TERMINATION OF SUSPENSION. -- The Secretary shall withdraw an order of suspension
of the distribution of a drug under subsection (g) if the person with respect to whom the order
was issued demonstrates in a petition to the Secretary -
(1)(A) on the basis of an audit by the Food and Drug Administration or by experts acceptable
to the Food and Drug Administration, or on the basis of other information, that the
development, approval, manufacturing, and distribution of such drug is in substantial
compliance with the applicable requirements of this Act, and
(B) changes in ownership, management, or operations –
(i) fully remedy the patterns or practices with respect to which the order was issued, and
(ii) provide reasonable assurances that such actions will not occur in the future, or
(2) the initial determination was in error.
The Secretary shall act on a submission of a petition under this subsection within 180 days of
the date of its submission and the Secretary may consider the petition concurrently with the
suspension proceeding. Any information submitted to the Secretary under this subsection
does not constitute an amendment or supplement to a pending or approved abbreviated drug
application.
(i) PROCEDURE. -- The Secretary may not take any action under subsection (a), (b), (c),
(d)(3), (g), or (h) with respect to any person unless the Secretary has issued an order for such
action made on the record after opportunity for an agency hearing on disputed issues of
material fact. In the course of any investigation or hearing under this subsection, the Secretary
may administer oaths and affirmations, examine witnesses, receive evidence, and issue
subpoenas requiring the attendance and testimony of witnesses and the production of
evidence that relates to the matter under investigation.
(j) JUDICAL REVIEW
(1) IN GENERAL. -- Except as provided in paragraph (2), any person that is the subject of an
adverse decision under subsection (a), (b), (c), (d), (f), (g), or (h) may obtain a review of such
decision by the United States Court of Appeals for the District of Columbia or for the circuit in
which the person resides, by filing in such court (within 60 days following the date the person is
notified of the Secretary's decision) a petition requesting that the decision be modified or set
aside.
(2) EXCEPTION. -- Any person that is the subject of an adverse decision under clause (iii) or
(iv) of subsection (b)(2)(B) may obtain a review of such decision by the United States District
Court for the District of Columbia or a district court of the United States for the district in which
the person resides, by filing in such court (within 30 days following the date the person is
notified of the Secretary's decision) a complaint requesting that the decision be modified or set
aside. In such an action, the court shall determine the matter de novo.
(k) CERTIFICATION. -- Any application for approval of a drug product shall include -
(1) a certification that the applicant did not and will not use in any capacity the services of any
person debarred under subsection (a) or (b), in connection with such application, and
(2) if such application is an abbreviated drug application, a list of all convictions, described in
subsections (a) and (b) which occurred within the previous 5 years, of the applicant and
affiliated persons responsible for the development or submission of such application.
(l) APPLICABILITY. --
(1) CONVICTION. -- For purposes of this section, a person is considered to have been
convicted of a criminal offense -
(A) when a judgment of conviction has been entered against the person by a Federal or State
court, regardless of whether there is an appeal pending,
(B) when a plea of guilty or nolo contendere by the person has been accepted by a Federal or
State court, or
(C) when the person has entered into participation in a first offender, deferred adjudication, or
other similar arrangement or program where judgment of conviction has been withheld.
(2) EFFECTIVE DATES. -- Subsection (a), subparagraph (A) of subsection (b)(2), and
subsection (b)(3)(A) clauses (i) and (ii) of subsection (b)(2)(B) shall not apply to a conviction
which occurred more than 5 years before the initiation of an agency action proposed to be
taken under subsection (a) or (b). Clauses (iii) and (iv) of subsection (b)(2)(B) , subsection
(b)(3)(B) and subsections (f) and (g) shall not apply to an act or action which occurred more
than 5 years before the initiation of an agency action proposed to be taken under subsection
(b), (f), or (g). Clause (iv) of subsection (b)(2)(B) shall not apply to an action which occurred
before June 1, 1992 . Subsection (k) shall not apply to applications submitted to the Secretary
before June 1, 1992 .
(m) Devices; Mandatory Debarment Regarding Third-Party Inspections and Reviews.--
(1) In general.--If the Secretary finds that a person has been convicted of a felony under
section 301( gg), the Secretary shall debar such person from being accredited under section
523(b) or 704(g)(2) and from carrying out activities under an agreement described in section
803(b).
(2) Debarment period.--The Secretary shall debar a person under paragraph (1) for the
following periods:
(A) The period of debarment of a person (other than an individual) shall not be less than 1 year
or more than 10 years, but if an act leading to a subsequent debarment under such paragraph
occurs within 10 years after such person has been debarred under such paragraph, the period
of debarment shall be permanent.
(B) The debarment of an individual shall be permanent.
(3) Termination of debarment; judicial review; other matters.--Subsections (c)(3), (d), (e), (i), (j),
and (l)(1) apply with respect to a person (other than an individual) or an individual who is
debarred under paragraph (1) to the same extent and in the same manner as such
subsections apply with respect to a person who is debarred under subsection (a)(1), or an
individual who is debarred under subsection (a)(2), respectively.
CIVIL PENALTIES
SEC. 307. [21 U.S.C. 335b] (a) IN GENERAL.—Any person that the Secretary finds—
(1) knowingly made or caused to be made, to any officer, employee, or agent of the
Department of Health and Human Services, a false statement or misrepresentation of a
material fact in connection with an abbreviated drug application,
(2) bribed or attempted to bribe or paid or attempted to pay an illegal gratuity to any officer,
employee, or agent of the Department of Health and Human Services in connection with an
abbreviated drug application,
(3) destroyed, altered, removed, or secreted, or procured the destruction, alteration, removal,
or secretion of, any material document or other material evidence which was the property of or
in the possession of the Department of Health and Human Services for the purpose of
interfering with that Department’s discharge of its responsibilities in connection with an
abbreviated drug application,
(4) knowingly failed to disclose, to an officer or employee of the Department of Health and
Human Services, a material fact which such person had an obligation to disclose relating to
any drug subject to an abbreviated drug application,
(5) knowingly obstructed an investigation of the Department of Health and Human Services
into any drug subject to an abbreviated drug application,
(6) is a person that has an approved or pending drug product application and has knowingly—
(A) employed or retained as a consultant or contractor, or
(B) otherwise used in any capacity the services of, a person who was debarred under section
306, or
(7) is an individual debarred under section 306 and, during the period of debarment, provided
services in any capacity to a person that had an approved or pending drug product application,
shall be liable to the United States for a civil penalty for each such violation in an amount not to
exceed $250,000 in the case of an individual and $1,000,000 in the case of any other person.
(b) PROCEDURE.—
(1) IN GENERAL.—
(A) ACTION BY THE SECRETARY.—A civil penalty under subsection (a) shall be assessed
by the Secretary on a person by an order made on the record after an opportunity for an
agency hearing on disputed issues of material fact and the amount of the penalty. In the
course of any investigation or hearing under this subparagraph, the Secretary may administer
oaths and affirmations, examine witnesses, receive evidence, and issue subpoenas requiring
the attendance and testimony of witnesses and the production of evidence that relates to the
matter under investigation.
(B) ACTION BY THE ATTORNEY GENERAL.—In lieu of a proceeding under subparagraph
(A), the Attorney General may, upon request of the Secretary, institute a civil action to recover
a civil money penalty in the amount and for any of the acts set forth in subsection (a). Such an
action may be instituted separately from or in connection with any other claim, civil or criminal,
initiated by the Attorney General under this Act.
(2) AMOUNT.—In determining the amount of a civil penalty under paragraph (1), the Secretary
or the court shall take into account the nature, circumstances, extent, and gravity of the act
subject to penalty, the person’s ability to pay, the effect on the person’s ability to continue to do
business, any history of prior, similar acts, and such other matters as justice may require.
(3) LIMITATION ON ACTIONS.—No action may be initiated under this section—
(A) with respect to any act described in subsection (a) that occurred before the date of the
enactment of this section, or
(B) more than 6 years after the date when facts material to the act are known or reasonably
should have been known by the Secretary but in no event more than 10 years after the date
the act took place.
(c) JUDICIAL REVIEW.—Any person that is the subject of an adverse decision under
subsection (b)(1)(A) may obtain a review of such decision by the United States Court of
Appeals for the District of Columbia or for the circuit in which the person resides, by filing in
such court (within 60 days following the date the person is notified of the Secretary’s decision)
a petition requesting that the decision be modified or set aside.
(d) RECOVERY OF PENALTIES.—The Attorney General may recover any civil penalty (plus
interest at the currently prevailing rates from the date the penalty became final) assessed
under subsection (b)(1)(A) in an action brought in the name of the United States . The amount
of such penalty may be deducted, when the penalty has become final, from any sums then or
later owing by the United States to the person against whom the penalty has been assessed.
In an action brought under this subsection, the validity, amount, and appropriateness of the
penalty shall not be subject to judicial review.
(e) INFORMANTS.—The Secretary may award to any individual (other than an officer or
employee of the Federal Government or a person who materially participated in any conduct
described in subsection (a)) who provides information leading to the imposition of a civil
penalty under this section an amount not to exceed—
(1) $250,000, or
(2) one-half of the penalty so imposed and collected, whichever is less. The decision of the
Secretary on such award shall not be reviewable.
AUTHORITY TO WITHDRAW APPROVAL OF ABBREVIATED DRUG APPLICATIONS
SEC. 308. [21 U.S.C. 335c] (a) IN GENERAL.—The Secretary—
(1) shall withdraw approval of an abbreviated drug application if the Secretary finds that the
approval was obtained, expedited, or otherwise facilitated through bribery, payment of an
illegal gratuity, or fraud or material false statement, and
(2) may withdraw approval of an abbreviated drug application if the Secretary finds that the
applicant has repeatedly demonstrated a lack of ability to produce the drug for which the
application was submitted in accordance with the formulations or manufacturing practice set
forth in the abbreviated drug application and has introduced, or attempted to introduce, such
adulterated or misbranded drug into commerce.
(b) PROCEDURE.—The Secretary may not take any action under subsection (a) with respect
to any person unless the Secretary has issued an order for such action made on the record
after opportunity for an agency hearing on disputed issues of material fact. In the course of any
investigation or hearing under this subsection, the Secretary may administer oaths and
affirmations, examine witnesses, receive evidence, and issue subpoenas requiring the
attendance and testimony of witnesses and the production of evidence that relates to the
matter under investigation.
(c) APPLICABILITY.—Subsection (a) shall apply with respect to offenses or acts regardless of
when such offenses or acts occurred.
(d) JUDICIAL REVIEW.—Any person that is the subject of an adverse decision under
subsection (a) may obtain a review of such decision by the United States Court of Appeals for
the District of Columbia or for the circuit in which the person resides, by filing in such court
(within 60 days following the date the person is notified of the Secretary’s decision) a petition
requesting that the decision be modified or set aside.
REPORT OF MINOR VIOLATIONS
SEC. 309. [21 U.S.C. 336] Nothing in this Act shall be construed as requiring the Secretary to
report for prosecution, or for the institution of libel or injunction proceedings, minor violations of
this Act whenever he believes that the public interest will be adequately served by a suitable
written notice or warning.
PROCEEDINGS IN NAME OF UNITED STATES; PROVISION AS TO SUBPOENAS
SEC. 310. [21 U.S.C. 337] (a) Except as provided in subsection (b), all such proceedings for
the enforcement, or to restrain violations, of this Act shall be by and in the name of the United
States . Subpoenas for witnesses who are required to attend a court of the United States , in
any district, may run into any other district in any proceeding under this section.
(b)(1) A State may bring in its own name and within its jurisdiction proceedings for the civil
enforcement, or to restrain violations, of section 401, 403(b), 403(c), 403(d), 403(e), 403(f),
403(g), 403(h), 403(i), 403(k), 403(q), or 403(r) if the food that is the subject of the proceedings
is located in the State.
(2) No proceeding may be commenced by a State under paragraph (1)—
(A) before 30 days after the State has given notice to the Secretary that the State intends to
bring such proceeding,
(B) before 90 days after the State has given notice to the Secretary of such intent if the
Secretary has, within such 30 days, commenced an informal or formal enforcement action
pertaining to the food which would be the subject of such proceeding, or
(C) if the Secretary is diligently prosecuting a proceeding in court pertaining to such food, has
settled such proceeding, or has settled the informal or formal enforcement action pertaining to
such food.
In any court proceeding described in subparagraph (C), a State may intervene as a matter of
right.
Footnotes: Chapter III
1. See footnote for section 403(h)(3) regarding the stylistic use of a list consisting of "(a)",
"(b)", etc.
2. The period is so in law. See section 102(b)(5)(C) of Public Law 108-282
3. The period is so in law. See section 102f(b)(5)(D) of Public Law 108-282.
4. So in law. See the amendment made by section 403 of Public Law 104–170 (110 Stat.
1514).
5. Paragraph (l) was struck by section 421 of Public Law 105–115 (111 Stat. 2380).
6. Paragraph (z) was added by subsection (b) of section 401(b) of Public Law 105–115 (111
Stat. 2364). Subsection (e) of such section provides as follows:
(e) SUNSET.—The amendments made by this section cease to be effective September 30,
2006, or 7 years after the date on which the Secretary promulgates the regulations described
in subsection (c), whichever is later.
7. So in law. Probably should be followed by a comma.
8. 1 The subsection is designated as subsection (f) to be consistent with the United States
Code. Prior to the enactment of Public Law 103–322, the last three subsections in section 303
were a subsection (e) that related to anabolic steroids, a subsection (f) that related to human
growth hormone, and a subsection (g) that related to civil penalties. Section 330015 of Public
Law 103-322 (108 Stat. 2146) amended the amendatory instructions of section 1904 of Public
Law 101– 647 with the result that the subsection (e) relating to anabolic steroids was struck,
and the subsection (f) relating to human growth hormone was redesignated as subsection (e).
Section 330015 did not, as a conforming amendment, expressly redesignate the subsection (g)
on civil penalties as subsection (f). The United States Code, however, shows the subsection
on civil penalties as subsection (f), and that approach is taken above to be consistent with the
Code.
9. So in law. See section 125(b)(2)(C) of Public Law 105-115 (111 Stat. 2325). Probably
should be "section".
CHAPTER IV—FOOD
DEFINITIONS AND STANDARDS FOR FOOD
SEC. 401. [21 U.S.C. 341] Whenever in the judgment of the Secretary such action will promote
honesty and fair dealing in the interest of consumers, he shall promulgate regulations fixing
and establishing for any food, under its common or usual name so far as practicable, a
reasonable definition and standard of identity, a reasonable standard of quality, or reasonable
standards of fill of container. No definition and standard of identity and no standard of quality
shall be established for fresh or dried fruits, fresh or dried vegetables, or butter, except that
definitions and standards of identity may be established for avocados, cantaloupes, citrus
fruits, and melons. In prescribing any standard of fill of container, the Secretary shall give due
consideration to the natural shrinkage in storage and in transit of fresh natural food and to
need for the necessary packing and protective material. In the prescribing of any standard of
quality for any canned fruit or canned vegetable, consideration shall be given and due
allowance made for the differing characteristics of the several varieties of such fruit or
vegetable. In prescribing a definition and standard of identity for any food or class of food in
which optional ingredients are permitted, the Secretary shall, for the purpose of promoting
honesty and fair dealing in the interest of consumers, designate the optional ingredients which
shall be named on the label. Any definition and standard of identity prescribed by the
Secretary for avocados, cantaloupes, citrus fruits, or melons shall relate only to maturity and to
the effects of freezing.
ADULTERATED FOOD
SEC. 402. [21 U.S.C. 342] A food shall be deemed to be adulterated— 1
(a) Poisonous, insanitary, or deleterious ingredients.
(1) If it bears or contains any poisonous or deleterious substance which may render it injurious
to health; but in case the substance is not an added substance such food shall not be
considered adulterated under this clause if the quantity of such substance in such food does
not ordinarily render it injurious to health; [or] 2 (2)(A) 3 if it bears or contains any added
poisonous or added deleterious substance (other than a substance that is a pesticide chemical
residue in or on a raw agricultural commodity or processed food, a food additive, a color
additive, or a new animal drug) that is unsafe within the meaning of section 406; or (B) if it
bears or contains a pesticide chemical residue that is unsafe within the meaning of section
408(a); or (C) if it is or if it bears or contains (i) any food additive that is unsafe within the
meaning of section 409; or (ii) a new animal drug (or conversion product thereof) that is unsafe
within the meaning of section 512; or (3) if it consists in whole or in part of any filthy, putrid, or
decomposed substance, or if it is otherwise unfit for food; or (4) if it has been prepared, packed,
or held under insanitary conditions whereby it may have become contaminated with filth, or
whereby it may have been rendered injurious to health; or (5) if it is, in whole or in part, the
product of a diseased animal or of an animal which has died otherwise than by slaughter; or (6)
if its container is composed, in whole or in part, of any poisonous or deleterious substance
which may render the contents injurious to health; or (7) if it has been intentionally subjected to
radiation, unless the use of the radiation was in conformity with a regulation or exemption in
effect pursuant to section 409.
(b) Absence, substitution, or addition of constituents.
(1) If any valuable constituent has been in whole or in part omitted or abstracted therefrom; or
(2) if any substance has been substituted wholly or in part therefore; or (3) if damage or
inferiority has been concealed in any manner; or (4) if any substance has been added thereto
or mixed or packed therewith so as to increase its bulk or weight, or reduce its quality or
strength, or make it appear better or of greater value than it is.
(c) Color additives. If it is, or it bears or contains, a color additive which is unsafe within the
meaning of section 721(a).
(d) Confectionery containing alcohol or nonnutritive substance. If it is confectionery, and—
(1) has partially or completely imbedded therein any nonnutritive object, except that this
subparagraph shall not apply in the case of any nonnutritive object if, in the judgment of the
Secretary as provided by regulations, such object is of practical functional value to the
confectionery product and would not render the product injurious or hazardous to health;
(2) bears or contains any alcohol other than alcohol not in excess of one-half of 1 per centum
by volume derived solely from the use of flavoring extracts, except that this clause shall not
apply to confectionery which is introduced or delivered for introduction into, or received or held
for sale in, interstate commerce if the sale of such confectionery is permitted under the laws of
the State in which such confectionery is intended to be offered for sale; or
(3) bears or contains any nonnutritive substance, except that this subparagraph shall not apply
to a safe nonnutritive substance which is in or on confectionery by reason of its use for some
practical functional purpose in the manufacture, packaging, or storage of such confectionery if
the use of the substance does not promote deception of the consumer or otherwise result in
adulteration or misbranding in violation of any provision of this Act, except that the Secretary
may, for the purpose of avoiding or resolving uncertainty as to the application of this
subparagraph, issue regulations allowing or prohibiting the use of particular nonnutritive
substances.
(e) Oleomargarine containing filthy, putrid, etc., matter. If it is oleomargarine or margarine or
butter and any of the raw material used therein consisted in whole or in part of any filthy, putrid,
or decomposed substance, or such oleomargarine or margarine or butter is otherwise unfit for
food.
(f) Dietary supplement or ingredient: safety.
(1) If it is a dietary supplement or contains a dietary ingredient that—
(A) presents a significant or unreasonable risk of illness or injury under—
(i) conditions of use recommended or suggested in labeling, or
(ii) if no conditions of use are suggested or recommended in the labeling, under ordinary
conditions of use;
(B) is a new dietary ingredient for which there is inadequate information to provide reasonable
assurance that such ingredient does not present a significant or unreasonable risk of illness or
injury;
(C) the Secretary declares to pose an imminent hazard to public health or safety, except that
the authority to make such declaration shall not be delegated and the Secretary shall promptly
after such a declaration initiate a proceeding in accordance with sections 554 and 556 of title 5,
United States Code, to affirm or withdraw the declaration; or
(D) is or contains a dietary ingredient that renders it adulterated under paragraph (a)(1) under
the conditions of use recommended or suggested in the labeling of such dietary supplement.
In any proceeding under this subparagraph, the United States shall bear the burden of proof
on each element to show that a dietary supplement is adulterated. The court shall decide any
issue under this paragraph on a de novo basis.
(2) Before the Secretary may report to a United States attorney a violation of paragraph 4 (1)(A)
for a civil proceeding, the person against whom such proceeding would be initiated shall be
given appropriate notice and the opportunity to present views, orally and in writing, at least 10
days before such notice, with regard to such proceeding.
(g) Dietary supplement: manufacturing practices.
(1) If it is a dietary supplement and it has been prepared, packed, or held under conditions that
do not meet current good manufacturing practice regulations, including regulations requiring,
when necessary, expiration date labeling, issued by the Secretary under subparagraph (2).
(2) The Secretary may by regulation prescribe good manufacturing practices for dietary
supplements. Such regulations shall be modeled after current good manufacturing practice
regulations for food and may not impose standards for which there is no current and generally
available analytical methodology. No standard of current good manufacturing practice may be
imposed unless such standard is included in a regulation promulgated after notice and
opportunity for comment in accordance with chapter 5 of title 5, United States Code.
(h) Reoffer of food previously denied admission. If it is an article of food imported or offered for
import into the United States and the article of food has previously been refused admission
under section 801(a), unless the person reoffering the article affirmatively establishes, at the
expense of the owner or consignee of the article, that the article complies with the applicable
requirements of this Act, as determined by the Secretary.
(i) Unsanitary transport. If it is transported or offered for transport by a shipper, carrier by motor
vehicle or rail vehicle, receiver, or any other person engaged in the transportation of food
under conditions that are not in compliance with regulations promulgated under section 416.
MISBRANDED FOOD
SEC. 403. [21 U.S.C. 343] A food shall be deemed to be misbranded— 5
(a) False or misleading label. If (1) its labeling is false or misleading in any particular, or (2) in
the case of a food to which section 411 applies, its advertising is false or misleading in a
material respect or its labeling is in violation of section 411(b)(2).
(b) Offer for sale under another name. If it is offered for sale under the name of another food.
(c) Imitation of another food. If it is an imitation of another food, unless its label bears, in type of
uniform size and prominence, the word "imitation" and, immediately thereafter, the name of the
food imitated.
(d) Misleading container. If its container is so made, formed, or filled as to be misleading.
(e) Package form. If in package form unless it bears a label containing (1) the name and place
of business of the manufacturer, packer, or distributor; and (2) an accurate statement of the
quantity of the contents in terms of weight, measure, or numerical count, except that under
clause (2) of this paragraph reasonable variations shall be permitted, and exemptions as to
small packages shall be established, by regulations prescribed by the Secretary.
(f) Prominence of information on label. If any word, statement, or other information required by
or under authority of this Act to appear on the label or labeling is not prominently placed
thereon with such conspicuousness (as compared with other words, statements, designs, or
devices, in the labeling) and in such terms as to render it likely to be read and understood by
the ordinary individual under customary conditions of purchase and use.
(g) Representation as to definition and standard of identity. If it purports to be or is represented
as a food for which a definition and standard of identity has been prescribed by regulations as
provided by section 401, unless (1) it conforms to such definition and standard, and (2) its label
bears the name of the food specified in the definition and standard, and, insofar as may be
required by such regulations, the common names of optional ingredients (other than spices,
flavoring, and coloring) present in such food.
(h) Representation as to standards of quality and fill of container. If it purports to be or is
represented as—
(1) a food for which a standard of quality has been prescribed by regulations as provided by
section 401, and its quality falls below such standard, unless its label bears, in such manner
and form as such regulations specify, a statement that it falls below such standard; or
(2) a food for which a standard or standards of fill of container have been prescribed by
regulations as provided by section 401, and it falls below the standard of fill of container
applicable thereto, unless its label bears, in such manner and form as such regulations specify,
a statement that it falls below such standard; or
(3) a food that is pasteurized unless—
(A) such food has been subjected to a safe process or treatment that is prescribed as
pasteurization for such food in a regulation promulgated under this Act; or
(B)(i) such food has been subjected to a safe process or treatment that—
(I) is reasonably certain to achieve destruction or elimination in the food of the most resistant
microorganisms of public health significance that are likely to occur in the food;
(II) is at least as protective of the public health as a process or treatment described in
subparagraph (A);
(III) is effective for a period that is at least as long as the shelf life of the food when stored
under normal and moderate abuse conditions; and
(IV) is the subject of a notification to the Secretary, including effectiveness data regarding the
process or treatment; and
(ii) at least 120 days have passed after the date of receipt of such notification by the Secretary
without the Secretary making a determination that the process or treatment involved has not
been shown to meet the requirements of subclauses (I) through (III) of clause (i) 6.
For purposes of paragraph (3) 6, a determination by the Secretary that a process or treatment
has not been shown to meet the requirements of subclauses (I) through (III) of subparagraph
(B)(i) 6 shall constitute final agency action under such subclauses.
(i) Label where no representation as to definition and standard of quality. Unless its label bears
(1) the common or usual name of the food, if any there be, and (2) in case it is fabricated from
two or more ingredients, the common or usual name of each such ingredient and if the food
purports to be a beverage containing vegetable or fruit juice, a statement with appropriate
prominence on the information panel of the total percentage of such fruit or vegetable juice
contained in the food; except that spices, flavorings, and colors not required to be certified
under section 721(c) 7 unless sold as spices, flavorings, or such colors, may be designated as
spices, flavorings, and colorings without naming each. To the extent that compliance with the
requirements of clause (2) of this paragraph is impracticable, or results in deception or unfair
competition, exemptions shall be established by regulations promulgated by the Secretary.
(j) Representation for special dietary use. If it purports to be or is represented for special
dietary uses, unless its label bears such information concerning its vitamin, mineral, and other
dietary properties as the Secretary determines to be, and by regulations prescribes as,
necessary in order fully to inform purchasers as to its value for such uses.
(k) Artificial flavoring, artificial coloring, or chemical preservatives. If it bears or contains any
artificial flavoring, artificial coloring, or chemical preservative, unless it bears labeling stating
that fact, except that to the extent that compliance with the requirements of this paragraph is
impracticable, exemptions shall be established by regulations promulgated by the Secretary.
The provisions of this paragraph and paragraphs (g) and (i) with respect to artificial coloring
shall not apply in the case of butter, cheese, or ice cream. The provisions of this paragraph
with respect to chemical preservatives shall not apply to a pesticide chemical when used in or
on a raw agricultural commodity which is the produce of the soil.
(l) Pesticide chemicals on raw agricultural commodities. If it is a raw agricultural commodity
which is the produce of the soil, bearing or containing a pesticide chemical applied after
harvest, unless the shipping container of such commodity bears labeling which declares the
presence of such chemical in or on such commodity and the common or usual name and the
function of such chemical, except that no such declaration shall be required while such
commodity, having been removed from the shipping container, is being held or displayed for
sale at retail out of such container in accordance with the custom of the trade.
(m) Color additives. If it is a color additive, unless its packaging and labeling are in conformity
with such packaging and labeling requirements, applicable to such color additive, as may be
contained in regulations issued under section 721.
(n) If its packaging or labeling is in violation of an applicable regulation issued pursuant to
section 3 or 4 of the Poison Prevention Packaging Act of 1970.
(o) [Repealed] 8
(p) [Deleted] 8
(q) Nutrition information.
(1) Except as provided in subparagraphs (3), (4), and (5), if it is a food intended for human
consumption and is offered for sale, unless its label or labeling bears nutrition information that
provides—
(A)(i) the serving size which is an amount customarily consumed and which is expressed in a
common household measure that is appropriate to the food, or (ii) if the use of the food is not
typically expressed in a serving size, the common household unit of measure that expresses
the serving size of the food,
(B) the number of servings or other units of measure per container,
(C) the total number of calories—
(i) derived from any source, and
(ii) derived from the total fat,
in each serving size or other unit of measure of the food,
(D) the amount of the following nutrients: Total fat, saturated fat, cholesterol, sodium, total
carbohydrates, complex carbohydrates, sugars, dietary fiber, and total protein contained in
each serving size or other unit of measure,
(E) any vitamin, mineral, or other nutrient required to be placed on the label and labeling of
food under this Act before October 1, 1990 , if the Secretary determines that such information
will assist consumers in maintaining healthy dietary practices.
The Secretary may by regulation require any information required to be placed on the label or
labeling by this subparagraph or subparagraph (2)(A) to be highlighted on the label or labeling
by larger type, bold type, or contrasting color if the Secretary determines that such highlighting
will assist consumers in maintaining healthy dietary practices.
(2)(A) If the Secretary determines that a nutrient other than a nutrient required by
subparagraph (1)(C), (1)(D), or (1)(E) should be included in the label or labeling of food subject
to subparagraph (1) for purposes of providing information regarding the nutritional value of
such food that will assist consumers in maintaining healthy dietary practices, the Secretary
may by regulation require that information relating to such additional nutrient be included in the
label or labeling of such food.
(B) If the Secretary determines that the information relating to a nutrient required by
subparagraph (1)(C), (1)(D), or (1)(E) or clause (A) of this subparagraph to be included in the
label or labeling of food is not necessary to assist consumers in maintaining healthy dietary
practices, the Secretary may by regulation remove information relating to such nutrient from
such requirement.
(3) For food that is received in bulk containers at a retail establishment, the Secretary may, by
regulation, provide that the nutrition information required by subparagraphs (1) and (2) be
displayed at the location in the retail establishment at which the food is offered for sale.
(4)(A) The Secretary shall provide for furnishing the nutrition information required by
subparagraphs (1) and (2) with respect to raw agricultural commodities and raw fish by issuing
voluntary nutrition guidelines, as provided by clause (B) or by issuing regulations that are
mandatory as provided by clause (D).
(B)(i) Upon the expiration of 12 months after the date of the enactment of the Nutrition Labeling
and Education Act of 1990 [enacted Nov. 8, 1990]9 , the Secretary, after providing an
opportunity for comment, shall issue guidelines for food retailers offering raw agricultural
commodities or raw fish to provide nutrition information specified in subparagraphs (1) and (2).
Such guidelines shall take into account the actions taken by food retailers during such
12-month period to provide to consumers nutrition information on raw agricultural commodities
and raw fish. Such guidelines shall only apply—
(I) in the case of raw agricultural commodities, to the 20 varieties of vegetables most frequently
consumed during a year and the 20 varieties of fruit most frequently consumed during a year,
and
(II) to the 20 varieties of raw fish most frequently consumed during a year.
The vegetables, fruits, and raw fish to which such guidelines apply shall be determined by the
Secretary by regulation and the Secretary may apply such guidelines regionally.
(ii) Upon the expiration of 12 months after the date of the enactment of the Nutrition Labeling
and Education Act of 1990 [enacted Nov. 8, 1990] 9, the Secretary shall issue a final regulation
defining the circumstances that constitute substantial compliance by food retailers with the
guidelines issued under subclause (i). The regulation shall provide that there is not substantial
compliance if a significant number of retailers have failed to comply with the guidelines. The
size of the retailers and the portion of the market served by retailers in compliance with the
guidelines shall be considered in determining whether the substantial-compliance standard
has been met.
(C)(i) Upon the expiration of 30 months after the date of the enactment of the Nutrition
Labeling and Education Act of 1990 [enacted Nov. 8, 1990] 9 , the Secretary shall issue a
report on actions taken by food retailers to provide consumers with nutrition information for raw
agricultural commodities and raw fish under the guidelines issued under clause (A). Such
report shall include a determination of whether there is substantial compliance with the
guidelines.
(ii) If the Secretary finds that there is substantial compliance with the guidelines, the Secretary
shall issue a report and make a determination of the type required in subclause (i) every two
years.
(D)(i) If the Secretary determines that there is not substantial compliance with the guidelines
issued under clause (A), the Secretary shall at the time such determination is made issue
proposed regulations requiring that any person who offers raw agricultural commodities or raw
fish to consumers provide, in a manner prescribed by regulations, the nutrition information
required by subparagraphs (1) and (2). The Secretary shall issue final regulations imposing
such requirements 6 months after issuing the proposed regulations. The final regulations shall
become effective 6 months after the date of their promulgation.
(ii) Regulations issued under subclause (i) may require that the nutrition information required
by subparagraphs (1) and (2) be provided for more than 20 varieties of vegetables, 20
varieties of fruit, and 20 varieties of fish most frequently consumed during a year if the
Secretary finds that a larger number of such products are frequently consumed. Such
regulations shall permit such information to be provided in a single location in each area in
which raw agricultural commodities and raw fish are offered for sale. Such regulations may
provide that information shall be expressed as an average or range per serving of the same
type of raw agricultural commodity or raw fish. The Secretary shall develop and make available
to the persons who offer such food to consumers the information required by subparagraphs (1)
and (2).
(iii) Regulations issued under subclause (i) shall permit the required information to be provided
in each area of an establishment in which raw agricultural commodities and raw fish are
offered for sale. The regulations shall permit food retailers to display the required information
by supplying copies of the information provided by the Secretary, by making the information
available in brochure, notebook or leaflet form, or by posting a sign disclosing the information.
Such regulations shall also permit presentation of the required information to be supplemented
by a video, live demonstration, or other media which the Secretary approves.
(E) For purposes of this subparagraph, the term "fish" includes freshwater or marine fin fish,
crustaceans, and mollusks, including shellfish, amphibians, and other forms of aquatic animal
life.
(F) No person who offers raw agricultural commodities or raw fish to consumers may be
prosecuted for minor violations of this subparagraph if there has been substantial compliance
with the requirements of this paragraph.
(5)(A) Subparagraphs (1), (2), (3), and (4) shall not apply to food—
(i) which is served in restaurants or other establishments in which food is served for immediate
human consumption or which is sold for sale or use in such establishments,
(ii) which is processed and prepared primarily in a retail establishment, which is ready for
human consumption, which is of the type described in subclause (i), and which is offered for
sale to consumers but not for immediate human consumption in such establishment and which
is not offered for sale outside such establishment,
(iii) which is an infant formula subject to section 412,
(iv) which is a medical food as defined in section 5(b) of the Orphan Drug Act (21 U.S.C.
360ee(b)), or
(v) which is described in section 405(2).
(B) Subparagraphs (1) and (2) shall not apply to the label of a food if the Secretary determines
by regulations that compliance with such subparagraphs is impracticable because the
package of such food is too small to comply with the requirements of such subparagraphs and
if the label of such food does not contain any nutrition information.
(C) If a food contains insignificant amounts, as determined by the Secretary, of all the nutrients
required by subparagraphs (1) and (2) to be listed in the label or labeling of food, the
requirements of such subparagraphs shall not apply to such food if the label, labeling, or
advertising of such food does not make any claim with respect to the nutritional value of such
food. If a food contains insignificant amounts, as determined by the Secretary, of more than
one-half the nutrients required by subparagraphs (1) and (2) to be in the label or labeling of the
food, the Secretary shall require the amounts of such nutrients to be stated in a simplified form
prescribed by the Secretary.
(D) If a person offers food for sale and has annual gross sales made or business done in sales
to consumers which is not more than $500,000 or has annual gross sales made or business
done in sales of food to consumers which is not more than $50,000, the requirements of
subparagraphs (1), (2), (3), and (4) shall not apply with respect to food sold by such person to
consumers unless the label or labeling of food offered by such person provides nutrition
information or makes a nutrition claim.
(E)(i) During the 12-month period for which an exemption from subparagraphs (1) and (2) is
claimed pursuant to this subclause, the requirements of such subparagraphs shall not apply to
any food product if—
(I) the labeling for such product does not provide nutrition information or make a claim subject
to paragraph (r),
(II) the person who claims for such product an exemption from such subparagraphs employed
fewer than an average of 100 full-time equivalent employees,
(III) such person provided the notice described in subclause (iii), and
(IV) in the case of a food product which was sold in the 12-month period preceding the period
for which an exemption was claimed, fewer than 100,000 units of such product were sold in the
United States during such preceding period, or in the case of a food product which was not
sold in the 12-month period preceding the period for which such exemption is claimed, fewer
than 100,000 units of such product are reasonably anticipated to be sold in the United States
during the period for which such exemption is claimed.
(ii) During the 12-month period after the applicable date referred to in this sentence, the
requirements of subparagraphs (1) and (2) shall not apply to any food product which was first
introduced into interstate commerce before May 8, 1994, if the labeling for such product does
not provide nutrition information or make a claim subject to paragraph (r), if such person
provided the notice described in subclause (iii), and if—
(I) during the 12-month period preceding May 8, 1994, the person who claims for such product
an exemption from such subparagraphs employed fewer than an average of 300 full-time
equivalent employees and fewer than 600,000 units of such product were sold in the United
States,
(II) during the 12-month period preceding May 8, 1995, the person who claims for such product
an exemption from such subparagraphs employed fewer than an average of 300 full-time
equivalent employees and fewer than 400,000 units of such product were sold in the United
States, or
(III) during the 12-month period preceding May 8, 1996 , the person who claims for such
product an exemption from such subparagraphs employed fewer than an average of 200
full-time equivalent employees and fewer than 200,000 units of such product were sold in the
United States .
(iii) The notice referred to in subclauses (i) and (ii) shall be given to the Secretary prior to the
beginning of the period during which the exemption under subclause (i) or (ii) is to be in effect,
shall state that the person claiming such exemption for a food product has complied with the
applicable requirements of subclause (i) or (ii), and shall—
(I) state the average number of full-time equivalent employees such person employed during
the 12 months preceding the date such person claims such exemption,
(II) state the approximate number of units the person claiming the exemption sold in the United
States ,
(III) if the exemption is claimed for a food product which was sold in the 12-month period
preceding the period for which the exemption was claimed, state the approximate number of
units of such product which were sold in the United States during such preceding period, and,
if the exemption is claimed for a food product which was not sold in such preceding period,
state the number of units of such product which such person reasonably anticipates will be
sold in the United States during the period for which the exemption was claimed, and
(IV) contain such information as the Secretary may require to verify the information required by
the preceding provisions of this subclause if the Secretary has questioned the validity of such
information.
If a person is not an importer, has fewer than 10 full-time equivalent employees, and sells
fewer than 10,000 units of any food product in any year, such person is not required to file a
notice for such product under this subclause for such year.
(iv) In the case of a person who claimed an exemption under subclause (i) or (ii), if, during the
period of such exemption, the number of full-time equivalent employees of such person
exceeds the number in such subclause or if the number of food products sold in the United
States exceeds the number in such subclause, such exemption shall extend to the expiration
of 18 months after the date the number of full-time equivalent employees or food products sold
exceeded the applicable number.
(v) For any food product first introduced into interstate commerce after May 8, 2002 , the
Secretary may by regulation lower the employee or units of food products requirement of
subclause (i) if the Secretary determines that the cost of compliance with such lower
requirement will not place an undue burden on persons subject to such lower requirement.
(vi) For purposes of subclauses (i), (ii), (iii), (iv), and (v)—
(I) the term "unit" means the packaging or, if there is no packaging, the form in which a food
product is offered for sale to consumers,
(II) the term "food product" means food in any sized package which is manufactured by a
single manufacturer or which bears the same brand name, which bears the same statement of
identity, and which has similar preparation methods, and
(III) the term "person" in the case of a corporation includes all domestic and foreign affiliates of
the corporation.
(F) A dietary supplement product (including a food to which section 411 applies) shall comply
with the requirements of subparagraphs (1) and (2) in a manner which is appropriate for the
product and which is specified in regulations of the Secretary which shall provide that—
(i) nutrition information shall first list those dietary ingredients that are present in the product in
a significant amount and for which a recommendation for daily consumption has been
established by the Secretary, except that a dietary ingredient shall not be required to be listed
if it is not present in a significant amount, and shall list any other dietary ingredient present and
identified as having no such recommendation;
(ii) the listing of dietary ingredients shall include the quantity of each such ingredient (or of a
proprietary blend of such ingredients) per serving;
(iii) the listing of dietary ingredients may include the source of a dietary ingredient; and
(iv) the nutrition information shall immediately precede the ingredient information required
under subclause (i), except that no ingredient identified pursuant to subclause (i) shall be
required to be identified a second time.
(G) Subparagraphs (1), (2), (3), and (4) shall not apply to food which is sold by a food
distributor if the food distributor principally sells food to restaurants or other establishments in
which food is served for immediate human consumption and does not manufacture, process,
or repackage the food it sells.
(r) Nutrition levels and health-related claims.
(1) Except as provided in clauses (A) through (C) of subparagraph (5), if it is a food intended
for human consumption which is offered for sale and for which a claim is made in the label or
labeling of the food which expressly or by implication—
(A) characterizes the level of any nutrient which is of the type required by paragraph (q)(1) or
(q)(2) to be in the label or labeling of the food unless the claim is made in accordance with
subparagraph (2), or
(B) characterizes the relationship of any nutrient which is of the type required by paragraph
(q)(1) or (q)(2) to be in the label or labeling of the food to a disease or a health-related
condition unless the claim is made in accordance with subparagraph (3) or (5)(D).
A statement of the type required by paragraph (q) that appears as part of the nutrition
information required or permitted by such paragraph is not a claim which is subject to this
paragraph and a claim subject to clause (A) is not subject to clause (B).
(2)(A) Except as provided in subparagraphs (4)(A)(ii) and (4)(A)(iii) and clauses (A) through (C)
of subparagraph (5), a claim described in subparagraph (1)(A)—
(i) may be made only if the characterization of the level made in the claim uses terms which
are defined in regulations of the Secretary,
(ii) may not state the absence of a nutrient unless—
(I) the nutrient is usually present in the food or in a food which substitutes for the food as
defined by the Secretary by regulation, or
(II) the Secretary by regulation permits such a statement on the basis of a finding that such a
statement would assist consumers in maintaining healthy dietary practices and the statement
discloses that the nutrient is not usually present in the food,
(iii) may not be made with respect to the level of cholesterol in the food if the food contains, as
determined by the Secretary by regulation, fat or saturated fat in an amount which increases to
persons in the general population the risk of disease or a health related condition which is diet
related unless—
(I) the Secretary finds by regulation that the level of cholesterol is substantially less than the
level usually present in the food or in a food which substitutes for the food and which has a
significant market share, or the Secretary by regulation permits a statement regarding the
absence of cholesterol on the basis of a finding that cholesterol is not usually present in the
food and that such a statement would assist consumers in maintaining healthy dietary
practices and the regulation requires that the statement disclose that cholesterol is not usually
present in the food, and
(II) the label or labeling of the food discloses the level of such fat or saturated fat in immediate
proximity to such claim and with appropriate prominence which shall be no less than one-half
the size of the claim with respect to the level of cholesterol,
(iv) may not be made with respect to the level of saturated fat in the food if the food contains
cholesterol unless the label or labeling of the food discloses the level of cholesterol in the food
in immediate proximity to such claim and with appropriate prominence which shall be no less
than one-half the size of the claim with respect to the level of saturated fat,
(v) may not state that a food is high in dietary fiber unless the food is low in total fat as defined
by the Secretary or the label or labeling discloses the level of total fat in the food in immediate
proximity to such statement and with appropriate prominence which shall be no less than
one-half the size of the claim with respect to the level of dietary fiber, and
(vi) may not be made if the Secretary by regulation prohibits the claim because the claim is
misleading in light of the level of another nutrient in the food.
(B) If a claim described in subparagraph (1)(A) is made with respect to a nutrient in a food and
the Secretary makes a determination that the food contains a nutrient at a level that increases
to persons in the general population the risk of a disease or health-related condition that is diet
related, the label or labeling of such food shall contain, prominently and in immediate proximity
to such claim, the following statement: "See nutrition information for ---- content." The blank
shall identify the nutrient associated with the increased disease or health-related condition risk.
In making the determination described in this clause, the Secretary shall take into account the
significance of the food in the total daily diet.
(C) Subparagraph (2)(A) does not apply to a claim described in subparagraph (1)(A) and
contained in the label or labeling of a food if such claim is contained in the brand name of such
food and such brand name was in use on such food before October 25, 1989, unless the brand
name contains a term defined by the Secretary under subparagraph (2)(A)(i). Such a claim is
subject to paragraph (a).
(D) Subparagraph (2) does not apply to a claim described in subparagraph (1)(A) which uses
the term "diet" and is contained in the label or labeling of a soft drink if (i) such claim is
contained in the brand name of such soft drink, (ii) such brand name was in use on such soft
drink before October 25, 1989, and (iii) the use of the term "diet" was in conformity with section
105.66 of title 21 of the Code of Federal Regulations. Such a claim is subject to paragraph (a).
(E) Subclauses (i) through (v) of subparagraph (2)(A) do not apply to a statement in the label
or labeling of food which describes the percentage of vitamins and minerals in the food in
relation to the amount of such vitamins and minerals recommended for daily consumption by
the Secretary.
(F) Subclause (i) clause (A) does not apply to a statement in the labeling of a dietary
supplement that characterizes the percentage level of a dietary ingredient for which the
Secretary has not established a reference daily intake, daily recommended value, or other
recommendation for daily consumption.
(G) A claim of the type described in subparagraph (1)(A) for a nutrient, for which the Secretary
has not promulgated a regulation under clause (A)(i), shall be authorized and may be made
with respect to a food if—
(i) a scientific body of the United States Government with official responsibility for public health
protection or research directly relating to human nutrition (such as the National Institutes of
Health or the Centers for Disease Control and Prevention) or the National Academy of
Sciences or any of its subdivisions has published an authoritative statement, which is currently
in effect, which identifies the nutrient level to which the claim refers;
(ii) a person has submitted to the Secretary, at least 120 days (during which the Secretary may
notify any person who is making a claim as authorized by clause (C) that such person has not
submitted all the information required by such clause) before the first introduction into
interstate commerce of the food with a label containing the claim, (I) a notice of the claim,
which shall include the exact words used in the claim and shall include a concise description of
the basis upon which such person relied for determining that the requirements of subclause (i)
have been satisfied, (II) a copy of the statement referred to in subclause (i) upon which such
person relied in making the claim, and (III) a balanced representation of the scientific literature
relating to the nutrient level to which the claim refers;
(iii) the claim and the food for which the claim is made are in compliance with clauses (A) and
(B), and are otherwise in compliance with paragraph (a) and section 201(n); and
(iv) the claim is stated in a manner so that the claim is an accurate representation of the
authoritative statement referred to in subclause (i) and so that the claim enables the public to
comprehend the information provided in the claim and to understand the relative significance
of such information in the context of a total daily diet.
For purposes of this clause, a statement shall be regarded as an authoritative statement of a
scientific body described in subclause (i) only if the statement is published by the scientific
body and shall not include a statement of an employee of the scientific body made in the
individual capacity of the employee.
(H) A claim submitted under the requirements of clause (G) may be made until—
(i) such time as the Secretary issues a regulation—
(I) prohibiting or modifying the claim and the regulation has become effective, or
(II) finding that the requirements of clause (G) have not been met, including finding that the
petitioner had not submitted all the information required by such clause; or
(ii) a district court of the United States in an enforcement proceeding under chapter III has
determined that the requirements of clause (G) have not been met.
(3)(A) Except as provided in subparagraph (5), a claim described in subparagraph (1)(B) may
only be made—
(i) if the claim meets the requirements of the regulations of the Secretary promulgated under
clause (B), and
(ii) if the food for which the claim is made does not contain, as determined by the Secretary by
regulation, any nutrient in an amount which increases to persons in the general population the
risk of a disease or health-related condition which is diet related, taking into account the
significance of the food in the total daily diet, except that the Secretary may by regulation
permit such a claim based on a finding that such a claim would assist consumers in
maintaining healthy dietary practices and based on a requirement that the label contain a
disclosure of the type required by subparagraph (2)(B).
(B)(i) The Secretary shall promulgate regulations authorizing claims of the type described in
subparagraph (1)(B) only if the Secretary determines, based on the totality of publicly available
scientific evidence (including evidence from well-designed studies conducted in a manner
which is consistent with generally recognized scientific procedures and principles), that there is
significant scientific agreement, among experts qualified by scientific training and experience
to evaluate such claims, that the claim is supported by such evidence.
(ii) A regulation described in subclause (i) shall describe—
(I) the relationship between a nutrient of the type required in the label or labeling of food by
paragraph (q)(1) or (q)(2) and a disease or health-related condition, and
(II) the significance of each such nutrient in affecting such disease or health-related condition.
(iii) A regulation described in subclause (i) shall require such claim to be stated in a manner so
that the claim is an accurate representation of the matters set out in subclause (ii) and so that
the claim enables the public to comprehend the information provided in the claim and to
understand the relative significance of such information in the context of a total daily diet.
(C) Notwithstanding the provisions of clauses (A)(i) and (B), a claim of the type described in
subparagraph (1)(B) which is not authorized by the Secretary in a regulation promulgated in
accordance with clause (B) shall be authorized and may be made with respect to a food if—
(i) a scientific body of the United States Government with official responsibility for public health
protection or research directly relating to human nutrition (such as the National Institutes of
Health or the Centers for Disease Control and Prevention) or the National Academy of
Sciences or any of its subdivisions has published an authoritative statement, which is currently
in effect, about the relationship between a nutrient and a disease or health-related condition to
which the claim refers;
(ii) a person has submitted to the Secretary, at least 120 days (during which the Secretary may
notify any person who is making a claim as authorized by clause (C) that such person has not
submitted all the information required by such clause) before the first introduction into
interstate commerce of the food with a label containing the claim, (I) a notice of the claim,
which shall include the exact words used in the claim and shall include a concise description of
the basis upon which such person relied for determining that the requirements of subclause (i)
have been satisfied, (II) a copy of the statement referred to in subclause (i) upon which such
person relied in making the claim, and (III) a balanced representation of the scientific literature
relating to the relationship between a nutrient and a disease or health-related condition to
which the claim refers;
(iii) the claim and the food for which the claim is made are in compliance with clause (A)(ii) and
are otherwise in compliance with paragraph (a) and section 201(n); and
(iv) the claim is stated in a manner so that the claim is an accurate representation of the
authoritative statement referred to in subclause (i) and so that the claim enables the public to
comprehend the information provided in the claim and to understand the relative significance
of such information in the context of a total daily diet.
For purposes of this clause, a statement shall be regarded as an authoritative statement of a
scientific body described in subclause (i) only if the statement is published by the scientific
body and shall not include a statement of an employee of the scientific body made in the
individual capacity of the employee.
(D) A claim submitted under the requirements of clause (C) may be made until—
(i) such time as the Secretary issues a regulation under the standard in clause (B)(i)—
(I) prohibiting or modifying the claim and the regulation has become effective, or
(II) finding that the requirements of clause (C) have not been met, including finding that the
petitioner has not submitted all the information required by such clause; or
(ii) a district court of the United States in an enforcement proceeding under chapter III has
determined that the requirements of clause (C) have not been met.
(4)(A)(i) Any person may petition the Secretary to issue a regulation under subparagraph
(2)(A)(i) or (3)(B) relating to a claim described in subparagraph (1)(A) or (1)(B). Not later than
100 days after the petition is received by the Secretary, the Secretary shall issue a final
decision denying the petition or file the petition for further action by the Secretary. If the
Secretary does not act within such 100 days, the petition shall be deemed to be denied unless
an extension is mutually agreed upon by the Secretary and the petitioner. If the Secretary
denies the petition or the petition is deemed to be denied, the petition shall not be made
available to the public. If the Secretary files the petition, the Secretary shall deny the petition or
issue a proposed regulation to take the action requested in the petition not later than 90 days
after the date of such decision. If the Secretary does not act within such 90 days, the petition
shall be deemed to be denied unless an extension is mutually agreed upon by the Secretary
and the petitioner. If the Secretary issues a proposed regulation, the rulemaking shall be
completed within 540 days of the date the petition is received by the Secretary. If the Secretary
does not issue a regulation within such 540 days, the Secretary shall provide the Committee
on Commerce of the House of Representatives and the Committee on Labor and Human
Resources of the Senate the reasons action on the regulation did not occur within such 540
days.
(ii) Any person may petition the Secretary for permission to use in a claim described in
subparagraph (1)(A) terms that are consistent with the terms defined by the Secretary under
subparagraph (2)(A)(i). Within 90 days of the submission of such a petition, the Secretary shall
issue a final decision denying the petition or granting such permission.
(iii) Any person may petition the Secretary for permission to use an implied claim described in
subparagraph (1)(A) in a brand name. After publishing notice of an opportunity to comment on
the petition in the Federal Register and making the petition available to the public, the
Secretary shall grant the petition if the Secretary finds that such claim is not misleading and is
consistent with terms defined by the Secretary under subparagraph (2)(A)(i). The Secretary
shall grant or deny the petition within 100 days of the date it is submitted to the Secretary and
the petition shall be considered granted if the Secretary does not act on it within such 100
days.
(B) A petition under clause (A)(i) respecting a claim described in subparagraph (1)(A) or (1)(B)
shall include an explanation of the reasons why the claim meets the requirements of this
paragraph and a summary of the scientific data which supports such reasons.
(C) If a petition for a regulation under subparagraph (3)(B) relies on a report from an
authoritative scientific body of the United States, the Secretary shall consider such report and
shall justify any decision rejecting the conclusions of such report.
(5)(A) This paragraph does not apply to infant formulas subject to section 412(h) and medical
foods as defined in section 5(b) of the Orphan Drug Act.
(B) Subclauses (iii) through (v) of subparagraph (2)(A) and subparagraph (2)(B) do not apply
to food which is served in restaurants or other establishments in which food is served for
immediate human consumption or which is sold for sale or use in such establishments.
(C) A subparagraph (1)(A) claim made with respect to a food which claim is required by a
standard of identity issued under section 401 shall not be subject to subparagraph (2)(A)(i) or
(2)(B).
(D) A subparagraph (1)(B) claim made with respect to a dietary supplement of vitamins,
minerals, herbs, or other similar nutritional substances shall not be subject to subparagraph (3)
but shall be subject to a procedure and standard, respecting the validity of such claim,
established by regulation of the Secretary.
(6) For purposes of paragraph (r)(1)(B), a statement for a dietary supplement may be made
if—
(A) the statement claims a benefit related to a classical nutrient deficiency disease and
discloses the prevalence of such disease in the United States, describes the role of a nutrient
or dietary ingredient intended to affect the structure or function in humans, characterizes the
documented mechanism by which a nutrient or dietary ingredient acts to maintain such
structure or function, or describes general well-being from consumption of a nutrient or dietary
ingredient,
(B) the manufacturer of the dietary supplement has substantiation that such statement is
truthful and not misleading, and
(C) the statement contains, prominently displayed and in boldface type, the following: "This
statement has not been evaluated by the Food and Drug Administration. This product is not
intended to diagnose, treat, cure, or prevent any disease.".
A statement under this subparagraph may not claim to diagnose, mitigate, treat, cure, or
prevent a specific disease or class of diseases. If the manufacturer of a dietary supplement
proposes to make a statement described in the first sentence of this subparagraph in the
labeling of the dietary supplement, the manufacturer shall notify the Secretary no later than 30
days after the first marketing of the dietary supplement with such statement that such a
statement is being made.
(7) The Secretary may make proposed regulations issued under this paragraph effective upon
publication pending consideration of public comment and publication of a final regulation if the
Secretary determines that such action is necessary—
(A) to enable the Secretary to review and act promptly on petitions the Secretary determines
provide for information necessary to—
(i) enable consumers to develop and maintain healthy dietary practices;
(ii) enable consumers to be informed promptly and effectively of important new knowledge
regarding nutritional and health benefits of food; or
(iii) ensure that scientifically sound nutritional and health information is provided to consumers
as soon as possible; or
(B) to enable the Secretary to act promptly to ban or modify a claim under this paragraph.
Such proposed regulations shall be deemed final agency action for purposes of judicial review.
(s) Dietary supplements.
If—
(1) it is a dietary supplement; and
(2)(A) the label or labeling of the supplement fails to list—
(i) the name of each ingredient of the supplement that is described in section 201(ff); and
(ii)(I) the quantity of each such ingredient; or
(II) with respect to a proprietary blend of such ingredients, the total quantity of all ingredients in
the blend;
(B) the label or labeling of the dietary supplement fails to identify the product by using the term
"dietary supplement", which term may be modified with the name of such an ingredient;
(C) the supplement contains an ingredient described in section 201(ff)(1)(C), and the label or
labeling of the supplement fails to identify any part of the plant from which the ingredient is
derived;
(D) the supplement—
(i) is covered by the specifications of an official compendium;
(ii) is represented as conforming to the specifications of an official compendium; and
(iii) fails to so conform; or
(E) the supplement—
(i) is not covered by the specifications of an official compendium; and
(ii)(I) fails to have the identity and strength that the supplement is represented to have; or
(II) fails to meet the quality (including tablet or capsule disintegration), purity, or compositional
specifications, based on validated assay or other appropriate methods, that the supplement is
represented to meet.
A dietary supplement shall not be deemed misbranded solely because its label or labeling
contains directions or conditions of use or warnings.
(t) Catfish.10 If it purports to be or is represented as catfish, unless it is fish classified within the
family Ictaluridae.
(u) Ginseng. 11 If it purports to be or is represented as ginseng, unless it is an herb or herbal
ingredient derived from a plant classified within the genus Panax.
(v) Failure to label; health threat.
If--
(1) it fails to bear a label required by the Secretary under section 801(n)(1) (relating to food
refused admission into the United States );
(2) the Secretary finds that the food presents a threat of serious adverse health consequences
or death to humans or animals; and
(3) upon or after notifying the owner or consignee involved that the label is required under
section 801, the Secretary informs the owner or consignee that the food presents such a
threat.
(w) Major food allergen labeling requirements.
(1) 12, 13, 14, 15 If it is not a raw agricultural commodity and it is, or it contains an ingredient
that bears or contains, a major food allergen, unless either—
(A) the word 'Contains', followed by the name of the food source from which the major food
allergen is derived, is printed immediately after or is adjacent to the list of ingredients (in a type
size no smaller than the type size used in the list of ingredients) required under subsections (g)
and (i); or
(B) the common or usual name of the major food allergen in the list of ingredients required
under subsections (g) and (i) is followed in parentheses by the name of the food source from
which the major food allergen is derived, except that the name of the food source is not
required when—
(i) the common or usual name of the ingredient uses the name of the food source from which
the major food allergen is derived; or
(ii) the name of the food source from which the major food allergen is derived appears
elsewhere in the ingredient list, unless the name of the food source that appears elsewhere in
the ingredient list appears as part of the name of a food ingredient that is not a major food
allergen under section 201( qq)(2)(A) or (B).
(2) As used in this subsection, the term 'name of the food source from which the major food
allergen is derived' means the name described in section 201( qq)(1); provided that in the case
of a tree nut, fish, or Crustacean shellfish, the term 'name of the food source from which the
major food allergen is derived' means the name of the specific type of nut or species of fish or
Crustacean shellfish.
(3) The information required under this subsection may appear in labeling in lieu of appearing
on the label only if the Secretary finds that such other labeling is sufficient to protect the public
health. A finding by the Secretary under this paragraph (including any change in an earlier
finding under this paragraph) is effective upon publication in the Federal Register as a notice.
(4) Notwithstanding subsection (g), (i), or (k), or any other law, a flavoring, coloring, or
incidental additive that is, or that bears or contains, a major food allergen shall be subject to
the labeling requirements of this subsection.
(5) The Secretary may by regulation modify the requirements of subparagraph (A) or (B) of
paragraph (1), or eliminate either the requirement of subparagraph (A) or the requirements of
subparagraph (B) of paragraph (1), if the Secretary determines that the modification or
elimination of the requirement of subparagraph (A) or the requirements of subparagraph (B) is
necessary to protect the public health.
(6)(A) Any person may petition the Secretary to exempt a food ingredient described in section
201( qq)(2) from the allergen labeling requirements of this subsection.
(B) The Secretary shall approve or deny such petition within 180 days of receipt of the petition
or the petition shall be deemed denied, unless an extension of time is mutually agreed upon by
the Secretary and the petitioner.
(C) The burden shall be on the petitioner to provide scientific evidence (including the analytical
method used to produce the evidence) that demonstrates that such food ingredient, as derived
by the method specified in the petition, does not cause an allergic response that poses a risk
to human health.
(D) A determination regarding a petition under this paragraph shall constitute final agency
action.
(E) The Secretary shall promptly post to a public site all petitions received under this
paragraph within 14 days of receipt and the Secretary shall promptly post the Secretary's
response to each.
(7)(A) A person need not file a petition under paragraph (6) to exempt a food ingredient
described in section 201( qq)(2) from the allergen labeling requirements of this subsection, if
the person files with the Secretary a notification containing—
(i) scientific evidence (including the analytical method used) that demonstrates that the food
ingredient (as derived by the method specified in the notification, where applicable) does not
contain allergenic protein; or
(ii) a determination by the Secretary that the ingredient does not cause an allergic response
that poses a risk to human health under a premarket approval or notification program under
section 409.
(B) The food ingredient may be introduced or delivered for introduction into interstate
commerce as a food ingredient that is not a major food allergen 90 days after the date of
receipt of the notification by the Secretary, unless the Secretary determines within the 90-day
period that the notification does not meet the requirements of this paragraph, or there is
insufficient scientific evidence to determine that the food ingredient does not contain allergenic
protein or does not cause an allergenic response that poses a risk to human health.
(C) The Secretary shall promptly post to a public site all notifications received under this
subparagraph within 14 days of receipt and promptly post any objections thereto by the
Secretary.
(x) Nonmajor food allergen labeling requirements.16 Notwithstanding subsection (g), (i), or (k),
17 or any other law, a spice, flavoring, coloring, or incidental additive that is, or that bears or
contains, a food allergen (other than a major food allergen), as determined by the Secretary by
regulation, shall be disclosed in a manner specified by the Secretary by regulation.
(y) [Caution: This subsection is effective and applicable to any dietary supplement
labeled on or after the date that is 1 year after enactment, pursuant to § 3(d)(1), (2) of Act
Dec. 22, 2006, P.L. 109–462]. If it is a dietary supplement that is marketed in the United
States, unless the label of such dietary supplement includes a domestic address or domestic
phone number through which the responsible person (as described in section 761) may
receive a report of a serious adverse event with such dietary supplement.
SEC. 403A. 18 [21 U.S.C. 343–1] (a) Except as provided in subsection (b), no State or political
subdivision of a State may directly or indirectly establish under any authority or continue in
effect as to any food in interstate commerce—
(1) any requirement for a food which is the subject of a standard of identity established under
section 401 that is not identical to such standard of identity or that is not identical to the
requirement of section 403(g), except that this paragraph does not apply to a standard of
identity of a State or political subdivision of a State for maple syrup that is of the type required
by sections 401 and 403(g),
(2) any requirement for the labeling of food of the type required by section 403(c), 403(e), or
403(i)(2) 403(i)(2), 403(w), or 403(x) that is not identical to the requirement of such section,
except that this paragraph does not apply to a requirement of a State or political subdivision of
a State that is of the type required by section 403(c) and that is applicable to maple syrup,
(3) any requirement for the labeling of food of the type required by section 403(b), 403(d),
403(f), 403(h), 403(i)(1), or 403(k) that is not identical to the requirement of such section,
except that this paragraph does not apply to a requirement of a State or political subdivision of
a State that is of the type required by section 403(h)(1) and that is applicable to maple syrup,
(4) any requirement for nutrition labeling of food that is not identical to the requirement of
section 403(q), except a requirement for nutrition labeling of food which is exempt under
subclause (i) or (ii) of section 403(q)(5)(A), or
(5) any requirement respecting any claim of the type described in section 403(r)(1) made in the
label or labeling of foodthat is not identical to the requirement of section 403(r), except a
requirement respecting a claim made in the label or labeling of food which is exempt under
section 403(r)(5)(B).
Paragraph (3) shall take effect in accordance with section 6(b) of the Nutrition Labeling and
Education Act of 1990.
(b) Upon petition of a State or a political subdivision of a State, the Secretary may exempt from
subsection (a), under such conditions as may be prescribed by regulation, any State or local
requirement that—
(1) would not cause any food to be in violation of any applicable requirement under Federal
law,
(2) would not unduly burden interstate commerce, and
(3) is designed to address a particular need for information which need is not met by the
requirements of the sections referred to in subsection (a).
DIETARY SUPPLEMENT LABELING EXEMPTIONS
SEC. 403B. [21 U.S.C. 343–2] (a) IN GENERAL.—A publication, including an article, a
chapter in a book, or an official abstract of a peer-reviewed scientific publication that appears
in an article and was prepared by the author or the editors of the publication, which is reprinted
in its entirety, shall not be defined as labeling when used in connection with the sale of a
dietary supplement to consumers when it—
(1) is not false or misleading;
(2) does not promote a particular manufacturer or brand of a dietary supplement;
(3) is displayed or presented, or is displayed or presented with other such items on the same
subject matter, so as to present a balanced view of the available scientific information on a
dietary supplement;
(4) if displayed in an establishment, is physically separate from the dietary supplements; and
(5) does not have appended to it any information by sticker or any other method.
(b) APPLICATION.—Subsection (a) shall not apply to or restrict a retailer or wholesaler of
dietary supplements in any way whatsoever in the sale of books or other publications as a part
of the business of such retailer or wholesaler.
(c) BURDEN OF PROOF.—In any proceeding brought under subsection (a), the burden of
proof shall be on the United States to establish that an article or other such matter is false or
misleading.
DISCLOSURE
SEC. 403C. [21 U.S.C. 343–3] (a) No provision of section 201(n), 403(a), or 409 shall be
construed to require on the label or labeling of a food a separate radiation disclosure
statement that is more prominent than the declaration of ingredients required by section
403(i)(2).
(b) In this section, the term "radiation disclosure statement" means a written statement that
discloses that a food has been intentionally subject to radiation.
EMERGENCY PERMIT CONTROL
SEC. 404. [21 U.S.C. 344] (a) Whenever the Secretary finds after investigation that the
distribution in interstate commerce of any class of food may, by reason of contamination with
micro-organisms during the manufacture, processing, or packing thereof in any locality, be
injurious to health, and that such injurious nature cannot be adequately determined after such
articles have entered interstate commerce, he then, and in such case only, shall promulgate
regulations providing for the issuance, to manufacturers, processors, or packers of such class
of food in such locality of permits to which shall be attached such conditions governing the
manufacture, processing, or packaging of such class of food, for such temporary period of time,
as may be necessary to protect the public health; and after the effective date of such
regulations, and during such temporary period, no person shall introduce or deliver for
introduction into interstate commerce any such food manufactured, processed, or packed by
any such manufacturer, processor, or packer unless such manufacturer, processor, or packer
holds a permit issued by the Secretary as provided by such regulations.
(b) The Secretary is authorized to suspend immediately upon notice any permit issued under
authority of this section if it is found that any of the conditions of the permit have been violated.
The holder of a permit so suspended shall be privileged at any time to apply for the
reinstatement of such permit, and the Secretary shall, immediately after prompt hearing and
an inspection of the establishment, reinstate such permit if it is found that adequate measures
have been taken to comply with and maintain the conditions of the permit, as originally issued
or as amended.
(c) Any officer or employee duly designated by the Secretary shall have access to any factory
or establishment, the operator of which holds a permit from the Secretary, for the purpose of
ascertaining whether or not the conditions of the permit are being complied with, and denial of
access for such inspection shall be ground for suspension of the permit until such access is
freely given by the operator.
REGULATIONS MAKING EXEMPTIONS
SEC. 405. [21 U.S.C. 345] The Secretary shall promulgate regulations exempting from any
labeling requirement of this Act (1) small open containers of fresh fruits and fresh vegetables
and (2) food which is in accordance with the practice of the trade, to be processed, labeled, or
repacked in substantial quantities at establishments other than those where originally
processed or packed, or condition that such food is not adulterated or misbranded under the
provisions of this Act upon removal from such processing, labeling, or repacking establishment.
This section does not apply to the labeling requirements of sections 403(q) and 403(r).
TOLERANCES FOR POISONOUS INGREDIENTS IN FOOD
SEC. 406. 19 [21 U.S.C. 346] Any poisonous or deleterious substance added to any food,
except where such substance is required in the production thereof or cannot be avoided by
good manufacturing practice shall be deemed to be unsafe for purposes of the application of
clause 2)(A) of section 402(a); but when such substance is so required or cannot be so
avoided, the Secretary shall promulgate regulations limiting the quantity therein or thereon to
such extent as he finds necessary for the protection of public health, and any quantity
exceeding the limits so fixed shall also be deemed to be unsafe for purposes of the application
of clause (2)(A) of section 402(a). While such a regulation is in effect limiting the quantity of
any such substance in the case of any food, such food shall not, by reason of bearing or
containing any added amount of such substance, be considered to be adulterated within the
meaning of clause (1) of section 402(a). In determining the quantity of such added substance
to be tolerated in or on different articles of food the Secretary shall take into account the extent
to which the use of such substance is required or cannot be avoided in the production of each
such article, and the other ways in which the consumer may be affected by the same or other
poisonous or deleterious substances.
OLEOMARGARINE OR MARGARINE
SEC. 407. 20 [21 U.S.C. 347] (a) Colored oleomargarine or colored margarine which is sold in
the same State or Territory in which it is produced shall be subject in the same manner and to
the same extent to the provisions of this Act as if it had been introduced in interstate
commerce.
(b) No person shall sell, or offer for sale, colored oleomargarine or colored margarine unless—
(1) such oleomargarine or margarine is packaged,
(2) the net weight of the contents of any package sold in a retail establishment is one pound or
less,
(3) there appears on the label of the package (A) the word ‘‘oleomargarine’’ or ‘‘margarine’’ in
type or lettering at least as large as any other type or lettering on such label, and (B) a full and
accurate statement of all the ingredients contained in such oleomargarine, or margarine, and
(4) each part of the contents of the package is contained in a wrapper which bears the word
‘‘oleomargarine’’ or ‘‘margarine’’ in type or lettering not smaller than 20-point type.
The requirements of this subsection shall be in addition to and not in lieu of any of the other
requirements of this Act.
(c) No person shall possess in a form ready for serving colored oleomargarine or colored
margarine at a public eating place unless a notice that oleomargarine or margarine is served is
displayed prominently and conspicuously in such place and in such manner as to render it
likely to be read and understood by the ordinary individual being served in such eating place or
is printed or is otherwise set forth on the menu in type or lettering not smaller than that
normally used to designate the serving of other food items. No person shall serve colored
oleomargarine or colored margarine at a public eating place, whether or not any charge is
made therefore, unless (1) each separate serving bears or is accompanied by labeling
identifying it as oleomargarine or margarine, or (2) each separate serving thereof is triangular
in shape.
(d) Colored oleomargarine or colored margarine when served with meals at a public eating
place shall at the time of such service be exempt from the labeling requirements of section 403
(except (a) and 403 (f)) 21 if it complies with the requirements of subsection (b) of this section.
(e) For the purpose of this section colored oleomargarine or colored margarine is
oleomargarine or margarine having a tint or shade containing more than one and six-tenths
degrees of yellow, or of yellow and red collectively, but with an excess of yellow over red,
measured in terms of Lovibond tintometer scale or its equivalent.
TOLERANCES AND EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES
SEC. 408. 22 [21 U.S.C. 346a] (a) REQUIREMENT FOR TOLERANCE OR EXEMPTION.—
(1) GENERAL RULE.—Except as provided in paragraph (2) or (3), any pesticide chemical
residue in or on a food shall be deemed unsafe for the purpose of section 402(a)(2)(B)
unless—
(A) a tolerance for such pesticide chemical residue in or on such food is in effect under this
section and the quantity of the residue is within the limits of the tolerance; or
(B) an exemption from the requirement of a tolerance is in effect under this section for the
pesticide chemical residue.
For the purposes of this section, the term ‘‘food’’, when used as a noun without modification,
shall mean a raw agricultural commodity or processed food.
(2) PROCESSED FOOD.—Notwithstanding paragraph (1)—
(A) if a tolerance is in effect under this section for a pesticide chemical residue in or on a raw
agricultural commodity, a pesticide chemical residue that is present in or on a processed food
because the food is made from that raw agricultural commodity shall not be considered unsafe
within the meaning of section 402(a)(2)(B) despite the lack of a tolerance for the pesticide
chemical residue in or on the processed food if the pesticide chemical has been used in or on
the raw agricultural commodity in conformity with a tolerance under this section, such residue
in or on the raw agricultural commodity has been removed to the extent possible in good
manufacturing practice, and the concentration of the pesticide chemical residue in the
processed food is not greater than the tolerance prescribed for the pesticide chemical residue
in the raw agricultural commodity; or
(B) if an exemption for the requirement for a tolerance is in effect under this section for a
pesticide chemical residue in or on a raw agricultural commodity, a pesticide chemical residue
that is present in or on a processed food because the food is made from that raw agricultural
commodity shall not be considered unsafe within the meaning of section 402(a)(2)(B).
(3) RESIDUES OF DEGRADATION PRODUCTS.—If a pesticide chemical residue is present
in or on a food because it is a metabolite or other degradation product of a precursor
substance that itself is a pesticide chemical or pesticide chemical residue, such a residue shall
not be considered to be unsafe within the meaning of section 402(a)(2)(B) despite the lack of a
tolerance or exemption from the need for a tolerance for such residue in or on such food if—
(A) the Administrator has not determined that the degradation product is likely to pose any
potential health risk from dietary exposure that is of a different type than, or of a greater
significance than, any risk posed by dietary exposure to the precursor substance;
(B) either—
(i) a tolerance is in effect under this section for residues of the precursor substance in or on the
food, and the combined level of residues of the degradation product and the precursor
substance in or on the food is at or below the stoichiometrically equivalent level that would be
permitted by the tolerance if the residue consisted only of the precursor substance rather than
the degradation product; or
(ii) an exemption from the need for a tolerance is in effect under this section for residues of the
precursor substance in or on the food; and
(C) the tolerance or exemption for residues of the precursor substance does not state that it
applies only to particular named substances and does not state that it does not apply to
residues of the degradation product.
(4) EFFECT OF TOLERANCE OR EXEMPTION.—While a tolerance or exemption from the
requirement for a tolerance is in effect under this section for a pesticide chemical residue with
respect to any food, the food shall not by reason of bearing or containing any amount of such a
residue be considered to be adulterated within the meaning of section 402(a)(1).
(b) AUTHORITY AND STANDARD FOR TOLERANCE.—
(1) AUTHORITY.—The Administrator may issue regulations establishing, modifying, or
revoking a tolerance for a pesticide chemical residue in or on a food—
(A) in response to a petition filed under subsection (d); or
(B) on the Administrator’s own initiative under subsection (e).
As used in this section, the term ‘‘modify’’ shall not mean expanding the tolerance to cover
additional foods.
(2) STANDARD.—
(A) GENERAL RULE.—
(i) STANDARD.—The Administrator may establish or leave in effect a tolerance for a pesticide
chemical residue in or on a food only if the Administrator determines that the tolerance is safe.
The Administrator shall modify or revoke a tolerance if the Administrator determines it is not
safe.
(ii) DETERMINATION OF SAFETY.—As used in this section, the term ‘‘safe’’, with respect to a
tolerance for a pesticide chemical residue, means that the Administrator has determined that
there is a reasonable certainty that no harm will result from aggregate exposure to the
pesticide chemical residue, including all anticipated dietary exposures and all other exposures
for which there is reliable information.
(iii) RULE OF CONSTRUCTION.—With respect to a tolerance, a pesticide chemical residue
meeting the standard under clause (i) is not an eligible pesticide chemical residue for purposes
of subparagraph (B).
(B) TOLERANCES FOR ELIGIBLE PESTICIDE CHEMICAL RESIDUES.—
(i) DEFINITION.—As used in this subparagraph, the term ‘‘eligible pesticide chemical residue’’
means a pesticide chemical residue as to which—
(I) the Administrator is not able to identify a level of exposure to the residue at which the
residue will not cause or contribute to a known or anticipated harm to human health (referred
to in this section as a ‘‘non-threshold effect’’);
(II) the lifetime risk of experiencing the non-threshold effect is appropriately assessed by
quantitative risk assessment; and
(III) with regard to any known or anticipated harm to human health for which the Administrator
is able to identify a level at which the residue will not cause such harm (referred to in this
section as a ‘‘threshold effect’’), the Administrator determines that the level of aggregate
exposure is safe.
(ii) DETERMINATION OF TOLERANCE.—Notwithstanding subparagraph (A)(i), a tolerance
for an eligible pesticide chemical residue may be left in effect or modified under this
subparagraph if—
(I) at least one of the conditions described in clause (iii) is met; and
(II) both of the conditions described in clause (iv) are met.
(iii) CONDITIONS REGARDING USE.—For purposes of clause (ii), the conditions described in
this clause with respect to a tolerance for an eligible pesticide chemical residue are the
following:
(I) Use of the pesticide chemical that produces the residue protects consumers from adverse
effects on health that would pose a greater risk than the dietary risk from the residue.
(II) Use of the pesticide chemical that produces the residue is necessary to avoid a significant
disruption in domestic production of an adequate, wholesome, and economical food supply.
(iv) CONDITIONS REGARDING RISK.—For purposes of clause (ii), the conditions described
in this clause with respect to a tolerance for an eligible pesticide chemical residue are the
following:
(I) The yearly risk associated with the nonthreshold effect from aggregate exposure to the
residue does not exceed 10 times the yearly risk that would be allowed under subparagraph (A)
for such effect.
(II) The tolerance is limited so as to ensure that the risk over a lifetime associated with the
nonthreshold effect from aggregate exposure to the residue is not greater than twice the
lifetime risk that would be allowed under subparagraph (A) for such effect.
(v) REVIEW.—Five years after the date on which the Administrator makes a determination to
leave in effect or modify a tolerance under this subparagraph, and thereafter as the
Administrator deems appropriate, the Administrator shall determine, after notice and
opportunity for comment, whether it has been demonstrated to the Administrator that a
condition described in clause (iii)(I) or clause (iii)(II) continues to exist with respect to the
tolerance and that the yearly and lifetime risks from aggregate exposure to such residue
continue to comply with the limits specified in clause (iv). If the Administrator determines by
such date that such demonstration has not been made, the Administrator shall, not later than
180 days after the date of such determination, issue a regulation under subsection (e)(1) to
modify or revoke the tolerance.
(vi) INFANTS AND CHILDREN.—Any tolerance under this subparagraph shall meet the
requirements of subparagraph (C).
(C) EXPOSURE OF INFANTS AND CHILDREN.—In establishing, modifying, leaving in effect,
or revoking a tolerance or exemption for a pesticide chemical residue, the Administrator—
(i) shall assess the risk of the pesticide chemical residue based on—
(I) available information about consumption patterns among infants and children that are likely
to result in disproportionately high consumption of foods containing or bearing such residue
among infants and children in comparison to the general population;
(II) available information concerning the special susceptibility of infants and children to the
pesticide chemical residues, including neurological differences between infants and children
and adults, and effects of in utero exposure to pesticide chemicals; and
(III) available information concerning the cumulative effects on infants and children of such
residues and other substances that have a common mechanism of toxicity; and
(ii) shall—
(I) ensure that there is a reasonable certainty that no harm will result to infants and children
from aggregate exposure to the pesticide chemical residue; and
(II) publish a specific determination regarding the safety of the pesticide chemical residue for
infants and children.
The Secretary of Health and Human Services and the Secretary of Agriculture, in consultation
with the Administrator, shall conduct surveys to document dietary exposure to pesticides
among infants and children. In the case of threshold effects, for purposes of clause (ii)(I) an
additional tenfold margin of safety for the pesticide chemical residue and other sources of
exposure shall be applied for infants and children to take into account potential pre- and
postnatal toxicity and completeness of the data with respect to exposure and toxicity to infants
and children. Notwithstanding such requirement for an additional margin of safety, the
Administrator may use a different margin of safety for the pesticide chemical residue only if, on
the basis of reliable data, such margin will be safe for infants and children.
(D) FACTORS.—In establishing, modifying, leaving in effect, or revoking a tolerance or
exemption for a pesticide chemical residue, the Administrator shall consider, among other
relevant factors—
(i) the validity, completeness, and reliability of the available data from studies of the pesticide
chemical and pesticide chemical residue;
(ii) the nature of any toxic effect shown to be caused by the pesticide chemical or pesticide
chemical residue in such studies;
(iii) available information concerning the relationship of the results of such studies to human
risk;
(iv) available information concerning the dietary consumption patterns of consumers (and
major identifiable subgroups of consumers);
(v) available information concerning the cumulative effects of such residues and other
substances that have a common mechanism of toxicity;
(vi) available information concerning the aggregate exposure levels of consumers (and major
identifiable subgroups of consumers) to the pesticide chemical residue and to other related
substances, including dietary exposure under the tolerance and all other tolerances in effect
for the pesticide chemical residue, and exposure from other non-occupational sources;
(vii) available information concerning the variability of the sensitivities of major identifiable
subgroups of consumers;
(viii) such information as the Administrator may require on whether the pesticide chemical may
have an effect in humans that is similar to an effect produced by a naturally occurring estrogen
or other endocrine effects; and
(ix) safety factors which in the opinion of experts qualified by scientific training and experience
to evaluate the safety of food additives are generally recognized as appropriate for the use of
animal experimentation data.
(E) DATA AND INFORMATION REGARDING ANTICIPATED AND ACTUAL RESIDUE
LEVELS.—
(i) AUTHORITY.—In establishing, modifying, leaving in effect, or revoking a tolerance for a
pesticide chemical residue, the Administrator may consider available data and information on
the anticipated residue levels of the pesticide chemical in or on food and the actual residue
levels of the pesticide chemical that have been measured in food, including residue data
collected by the Food and Drug Administration.
(ii) REQUIREMENT.—If the Administrator relies on anticipated or actual residue levels in
establishing, modifying, or leaving in effect a tolerance, the Administrator shall pursuant to
subsection (f)(1) require that data be provided five years after the date on which the tolerance
is established, modified, or left in effect, and thereafter as the Administrator deems appropriate,
demonstrating that such residue levels are not above the levels so relied on. If such data are
not so provided, or if the data do not demonstrate that the residue levels are not above the
levels so relied on, the Administrator shall, not later than 180 days after the date on which the
data were required to be provided, issue a regulation under subsection (e)(1), or an order
under subsection (f)(2), as appropriate, to modify or revoke the tolerance.
(F) PERCENT OF FOOD ACTUALLY TREATED.—In establishing, modifying, leaving in effect,
or revoking a tolerance for a pesticide chemical residue, the Administrator may, when
assessing chronic dietary risk, consider available data and information on the percent of food
actually treated with the pesticide chemical (including aggregate pesticide use data collected
by the Department of Agriculture) only if the Administrator—
(i) finds that the data are reliable and provide a valid basis to show what percentage of the food
derived from such crop is likely to contain such pesticide chemical residue;
(ii) finds that the exposure estimate does not understate exposure for any significant
subpopulation group;
(iii) finds that, if data are available on pesticide use and consumption of food in a particular
area, the population in such area is not dietarily exposed to residues above those estimated by
the Administrator; and
(iv) provides for the periodic reevaluation of the estimate of anticipated dietary exposure.
(3) DETECTION METHODS.—
(A) GENERAL RULE.—A tolerance for a pesticide chemical residue in or on a food shall not
be established or modified by the Administrator unless the Administrator determines, after
consultation with the Secretary, that there is a practical method for detecting and measuring
the levels of the pesticide chemical residue in or on the food.
(B) DETECTION LIMIT.—A tolerance for a pesticide chemical residue in or on a food shall not
be established at or modified to a level lower than the limit of detection of the method for
detecting and measuring the pesticide chemical residue specified by the Administrator under
subparagraph (A).
(4) INTERNATIONAL STANDARDS.—In establishing a tolerance for a pesticide chemical
residue in or on a food, the Administrator shall determine whether a maximum residue level for
the pesticide chemical has been established by the Codex Alimentarius Commission. If a
Codex maximum residue level has been established for the pesticide chemical and the
Administrator does not propose to adopt the Codex level, the Administrator shall publish for
public comment a notice explaining the reasons for departing from the Codex level.
(c) AUTHORITY AND STANDARD FOR EXEMPTIONS.—
(1) AUTHORITY.—The Administrator may issue a regulation establishing, modifying, or
revoking an exemption from the requirement for a tolerance for a pesticide chemical residue in
or on food—
(A) in response to a petition filed under subsection (d); or
(B) on the Administrator’s initiative under subsection (e).
(2) STANDARD.—
(A) GENERAL RULE.—
(i) STANDARD.—The Administrator may establish or leave in effect an exemption from the
requirement for a tolerance for a pesticide chemical residue in or on food only if the
Administrator determines that the exemption is safe. The Administrator shall modify or revoke
an exemption if the Administrator determines it is not safe.
(ii) DETERMINATION OF SAFETY.—The term ‘‘safe’’, with respect to an exemption for a
pesticide chemical residue, means that the Administrator has determined that there is a
reasonable certainty that no harm will result from aggregate exposure to the pesticide
chemical residue, including all anticipated dietary exposures and all other exposures for which
there is reliable information.
(B) FACTORS.—In making a determination under this paragraph, the Administrator shall take
into account, among other relevant considerations, the considerations set forth in
subparagraphs (C) and (D) of subsection (b)(2).
(3) LIMITATION.— An exemption from the requirement for a tolerance for a pesticide chemical
residue in or on food shall not be established or modified by the Administrator unless the
Administrator determines, after consultation with the Secretary—
(A) that there is a practical method for detecting and measuring the levels of such pesticide
chemical residue in or on food; or
(B) that there is no need for such a method, and states the reasons for such determination in
issuing the regulation establishing or modifying the exemption.
(d) PETITION FOR TOLERANCE OR EXEMPTION.—
(1) PETITIONS AND PETITIONERS.— Any person may file with the Administrator a petition
proposing the issuance of a regulation—
(A) establishing, modifying, or revoking a tolerance for a pesticide chemical residue in or on a
food; or
(B) establishing, modifying, or revoking an exemption from the requirement of a tolerance for
such a residue.
(2) PETITION CONTENTS.—
(A) ESTABLISHMENT.—A petition under paragraph (1) to establish a tolerance or exemption
for a pesticide chemical residue shall be supported by such data and information as are
specified in regulations issued by the Administrator, including—
(i)(I) an informative summary of the petition and of the data, information, and arguments
submitted or cited in support of the petition; and
(II) a statement that the petitioner agrees that such summary or any information it contains
may be published as a part of the notice of filing of the petition to be published under this
subsection and as part of a proposed or final regulation issued under this section;
(ii) the name, chemical identity, and composition of the pesticide chemical residue and of the
pesticide chemical that produces the residue;
(iii) data showing the recommended amount, frequency, method, and time of application of
that pesticide chemical; (iv) full reports of tests and investigations made with respect to the
safety of the pesticide chemical, including full information as to the methods and controls used
in conducting those tests and investigations;
(v) full reports of tests and investigations made with respect to the nature and amount of the
pesticide chemical residue that is likely to remain in or on the food, including a description of
the analytical methods used;
(vi) a practical method for detecting and measuring the levels of the pesticide chemical residue
in or on the food, or for exemptions, a statement why such a method is not needed;
(vii) a proposed tolerance for the pesticide chemical residue, if a tolerance is proposed;
(viii) if the petition relates to a tolerance for a processed food, reports of investigations
conducted using the processing method(s) used to produce that food;
(ix) such information as the Administrator may require to make the determination under
subsection (b)(2)(C);
(x) such information as the Administrator may require on whether the pesticide chemical may
have an effect in humans that is similar to an effect produced by a naturally occurring estrogen
or other endocrine effects;
(xi) information regarding exposure to the pesticide chemical residue due to any tolerance or
exemption already granted for such residue;
(xii) practical methods for removing any amount of the residue that would exceed any
proposed tolerance; and
(xiii) such other data and information as the Administrator requires by regulation to support the
petition.
If information or data required by this subparagraph is available to the Administrator, the
person submitting the petition may cite the availability of the information or data in lieu of
submitting it. The Administrator may require a petition to be accompanied by samples of the
pesticide chemical with respect to which the petition is filed.
(B) MODIFICATION OR REVOCATION.— The Administrator may by regulation establish the
requirements for information and data to support a petition to modify or revoke a tolerance or
to modify or revoke an exemption from the requirement for a tolerance.
(3) NOTICE.—A notice of the filing of a petition that the Administrator determines has met the
requirements of paragraph (2) shall be published by the Administrator within 30 days after
such determination. The notice shall announce the availability of a description of the analytical
methods available to the Administrator for the detection and measurement of the pesticide
chemical residue with respect to which the petition is filed or shall set forth the petitioner’s
statement of why such a method is not needed. The notice shall include the summary required
by paragraph (2)(A)(i)(I).
(4) ACTIONS BY THE ADMINISTRATOR.—
(A) IN GENERAL.—The Administrator shall, after giving due consideration to a petition filed
under paragraph (1) and any other information available to the Administrator—
(i) issue a final regulation (which may vary from that sought by the petition) establishing,
modifying, or revoking a tolerance for the pesticide chemical residue or an exemption of the
pesticide chemical residue from the requirement of a tolerance (which final regulation shall be
issued without further notice and without further period for public comment);
(ii) issue a proposed regulation under subsection (e), and thereafter issue a final regulation
under such subsection; or
(iii) issue an order denying the petition.
(B) PRIORITIES.—The Administrator shall give priority to petitions for the establishment or
modification of a tolerance or exemption for a pesticide chemical residue that appears to pose
a significantly lower risk to human health from dietary exposure than pesticide chemical
residues that have tolerances in effect for the same or similar uses.
(C) EXPEDITED REVIEW OF CERTAIN PETITIONS.—
(i) DATE CERTAIN FOR REVIEW.—If a person files a complete petition with the Administrator
proposing the issuance of a regulation establishing a tolerance or exemption for a pesticide
chemical residue that presents a lower risk to human health than a pesticide chemical residue
for which a tolerance has been left in effect or modified under subsection (b)(2)(B), the
Administrator shall complete action on such petition under this paragraph within 1 year.
(ii) REQUIRED DETERMINATIONS.—If the Administrator issues a final regulation
establishing a tolerance or exemption for a safer pesticide chemical residue under clause (i),
the Administrator shall, not later than 180 days after the date on which the regulation is issued,
determine whether a condition described in subclause (I) or (II) of subsection (b)(2)(B)(iii)
continues to exist with respect to a tolerance that has been left in effect or modified under
subsection (b)(2)(B). If such condition does not continue to exist, the Administrator shall, not
later than 180 days after the date on which the determination under the preceding sentence is
made, issue a regulation under subsection (e)(1) to modify or revoke the tolerance.
(e) ACTION ON ADMINISTRATOR’S OWN INITIATIVE.—
(1) GENERAL RULE.—The Administrator may issue a regulation—
(A) establishing, modifying, suspending under subsection (l)(3), or revoking a tolerance for a
pesticide chemical or a pesticide chemical residue;
(B) establishing, modifying, suspending under subsection (l)(3), or revoking an exemption of a
pesticide chemical residue from the requirement of a tolerance; or
(C) establishing general procedures and requirements to implement this section.
(2) NOTICE.—Before issuing a final regulation under paragraph (1), the Administrator shall
issue a notice of proposed rulemaking and provide a period of not less than 60 days for public
comment on the proposed regulation, except that a shorter period for comment may be
provided if the Administrator for good cause finds that it would be in the public interest to do so
and states the reasons for the finding in the notice of proposed rulemaking.
(f) SPECIAL DATA REQUIREMENTS.—
(1) REQUIRING SUBMISSION OF ADDITIONAL DATA.—If the Administrator determines that
additional data or information are reasonably required to support the continuation of a
tolerance or exemption that is in effect under this section for a pesticide chemical residue on a
food, the Administrator shall—
(A) issue a notice requiring the person holding the pesticide registrations associated with such
tolerance or exemption to submit the data or information under section 3(c)(2)(B) of the
Federal Insecticide, Fungicide, and Rodenticide Act;
(B) issue a rule requiring that testing be conducted on a substance or mixture under section 4
of the Toxic Substances Control Act; or
(C) publish in the Federal Register, after first providing notice and an opportunity for comment
of not less than 60 days’ duration, an order—
(i) requiring the submission to the Administrator by one or more interested persons of a notice
identifying the person or persons who will submit the required data and information;
(ii) describing the type of data and information required to be submitted to the Administrator
and stating why the data and information could not be obtained under the authority of section
3(c)(2)(B) of the Federal Insecticide, Fungicide, and Rodenticide Act or section 4 of the Toxic
Substances Control Act;
(iii) describing the reports of the Administrator required to be prepared during and after the
collection of the data and information;
(iv) requiring the submission to the Administrator of the data, information, and reports referred
to in clauses (ii) and (iii); and
(v) establishing dates by which the submissions described in clauses (i) and (iv) must be
made.
The Administrator may under subparagraph (C) revise any such order to correct an error. The
Administrator may under this paragraph require data or information pertaining to whether the
pesticide chemical may have an effect in humans that is similar to an effect produced by a
naturally occurring estrogen or other endocrine effects.
(2) NONCOMPLIANCE.—If a submission required by a notice issued in accordance with
paragraph (1)(A), a rule issued under paragraph (1)(B), or an order issued under paragraph
(1)(C) is not made by the time specified in such notice, rule, or order, the Administrator may by
order published in the Federal Register modify or revoke the tolerance or exemption in
question. In any review of such an order under subsection (g)(2), the only material issue shall
be whether a submission required under paragraph (1) was not made by the time specified.
(g) EFFECTIVE DATE, OBJECTIONS, HEARINGS, AND ADMINISTRATIVE REVIEW.—
(1) EFFECTIVE DATE.—A regulation or order issued under subsection (d)(4), (e)(1), or (f)(2)
shall take effect upon publication unless the regulation or order specifies otherwise. The
Administrator may stay the effectiveness of the regulation or order if, after issuance of such
regulation or order, objections are filed with respect to such regulation or order pursuant to
paragraph (2).
(2) FURTHER PROCEEDINGS.—
(A) OBJECTIONS.—Within 60 days after a regulation or order is issued under subsection
(d)(4), (e)(1)(A), (e)(1)(B), (f)(2), (n)(3), or (n)(5)(C), any person may file objections thereto with
the Administrator, specifying with particularity the provisions of the regulation or order deemed
objectionable and stating reasonable grounds therefor. If the regulation or order was issued in
response to a petition under subsection (d)(1), a copy of each objection filed by a person other
than the petitioner shall be served by the Administrator on the petitioner.
(B) HEARING.—An objection may include a request for a public evidentiary hearing upon the
objection. The Administrator shall, upon the initiative of the Administrator or upon the request
of an interested person and after due notice, hold a public evidentiary hearing if and to the
extent the Administrator determines that such a public hearing is necessary to receive factual
evidence relevant to material issues of fact raised by the objections. The presiding officer in
such a hearing may authorize a party to obtain discovery from other persons and may upon a
showing of good cause made by a party issue a subpoena to compel testimony or production
of documents from any person. The presiding officer shall be governed by the Federal Rules of
Civil Procedure in making any order for the protection of the witness or the content of
documents produced and shall order the payment of reasonable fees and expenses as a
condition to requiring testimony of the witness. On contest, such a subpoena may be enforced
by a Federal district court.
(C) FINAL DECISION.—As soon as practicable after receiving the arguments of the parties,
the Administrator shall issue an order stating the action taken upon each such objection and
setting forth any revision to the regulation or prior order that the Administrator has found to be
warranted. If a hearing was held under subparagraph (B), such order and any revision to the
regulation or prior order shall, with respect to questions of fact at issue in the hearing, be
based only on substantial evidence of record at such hearing, and shall set forth in detail the
findings of facts and the conclusions of law or policy upon which the order or regulation is
based.
(h) JUDICIAL REVIEW.—
(1) PETITION.—In a case of actual controversy as to the validity of any regulation issued
under subsection (e)(1)(C), or any order issued under subsection (f)(1)(C) or (g)(2)(C), or any
regulation that is the subject of such an order, any person who will be adversely affected by
such order or regulation may obtain judicial review by filing in the United States Court of
Appeals for the circuit wherein that person resides or has its principal place of business, or in
the United States Court of Appeals for the District of Columbia Circuit, within 60 days after
publication of such order or regulation, a petition praying that the order or regulation be set
aside in whole or in part.
(2) RECORD AND JURISDICTION.—A copy of the petition under paragraph (1) shall be
forthwith transmitted by the clerk of the court to the Administrator, or any officer designated by
the Administrator for that purpose, and thereupon the Administrator shall file in the court the
record of the proceedings on which the Administrator based the order or regulation, as
provided in section 2112 of title 28, United States Code. Upon the filing of such a petition, the
court shall have exclusive jurisdiction to affirm or set aside the order or regulation complained
of in whole or in part. As to orders issued following a public evidentiary hearing, the findings of
the Administrator with respect to questions of fact shall be sustained only if supported by
substantial evidence when considered on the record as a whole.
(3) ADDITIONAL EVIDENCE.—If a party applies to the court for leave to adduce additional
evidence and shows to the satisfaction of the court that the additional evidence is material and
that there were reasonable grounds for the failure to adduce the evidence in the proceeding
before the Administrator, the court may order that the additional evidence (and evidence in
rebuttal thereof) shall be taken before the Administrator in the manner and upon the terms and
conditions the court deems proper. The Administrator may modify prior findings as to the facts
by reason of the additional evidence so taken and may modify the order or regulation
accordingly. The Administrator shall file with the court any such modified finding, order, or
regulation.
(4) FINAL JUDGMENT; SUPREME COURT REVIEW.—The judgment of the court affirming or
setting aside, in whole or in part, any regulation or any order and any regulation which is the
subject of such an order shall be final, subject to review by the Supreme Court of the United
States as provided in section 1254 of title 28 of the United States Code. The commencement
of proceedings under this subsection shall not, unless specifically ordered by the court to the
contrary, operate as a stay of a regulation or order.
(5) APPLICATION.—Any issue as to which review is or was obtainable under this subsection
shall not be the subject of judicial review under any other provision of law.
(i) CONFIDENTIALITY AND USE OF DATA.—
(1) GENERAL RULE.—Data and information that are or have been submitted to the
Administrator under this section or section 409 in support of a tolerance or an exemption from
a tolerance shall be entitled to confidential treatment for reasons of business confidentiality
and to exclusive use and data compensation to the same extent provided by sections 3 and 10
of the Federal Insecticide, Fungicide, and Rodenticide Act.
(2) EXCEPTIONS.—
(A) IN GENERAL.—Data and information that are entitled to confidential treatment under
paragraph (1) may be disclosed, under such security requirements as the Administrator may
provide by regulation, to—
(i) employees of the United States authorized by the Administrator to examine such data and
information in the carrying out of their official duties under this Act or other Federal statutes
intended to protect the public health; or
(ii) contractors with the United States authorized by the Administrator to examine such data
and information in the carrying out of contracts under this Act or such statutes.
(B) CONGRESS.—This subsection does not authorize the withholding of data or information
from either House of Congress or from, to the extent of matter within its jurisdiction, any
committee or subcommittee of such committee or any joint committee of Congress or any
subcommittee of such joint committee.
(3) SUMMARIES.—Notwithstanding any provision of this subsection or other law, the
Administrator may publish the informative summary required by subsection (d)(2)(A)(i) and
may, in issuing a proposed or final regulation or order under this section, publish an
informative summary of the data relating to the regulation or order.
(j) STATUS OF PREVIOUSLY ISSUED REGULATIONS.—
(1) REGULATIONS UNDER SECTION 406.—Regulations affecting pesticide chemical
residues in or on raw agricultural commodities promulgated, in accordance with section 701(e),
under the authority of section 406(a) upon the basis of public hearings instituted before
January 1, 1953, shall be deemed to be regulations issued under this section and shall be
subject to modification or revocation under subsections (d) and (e), and shall be subject to
review under subsection (q).
(2) REGULATIONS UNDER SECTION 409.—Regulations that established tolerances for
substances that are pesticide chemical residues in or on processed food, or that otherwise
stated the conditions under which such pesticide chemicals could be safely used, and that
were issued under section 409 on or before the date of the enactment of this paragraph, shall
be deemed to be regulations issued under this section and shall be subject to modification or
revocation under subsection (d) or (e), and shall be subject to review under subsection (q).
(3) REGULATIONS UNDER SECTION 408.—Regulations that established tolerances or
exemptions under this section that were issued on or before the date of the enactment of this
paragraph shall remain in effect unless modified or revoked under subsection (d) or (e), and
shall be subject to review under subsection (q).
(4) CERTAIN SUBSTANCES.—With respect to a substance that is not included in the
definition of the term ‘pesticide chemical’ under section 201(q)(1) but was so included on the
day before the date of the enactment of the Antimicrobial Regulation Technical Corrections Act
of 1998, the following applies as of such date of enactment:
(A) Notwithstanding paragraph (2), any regulation applying to the use of the substance that
was in effect on the day before such date, and was on such day deemed in such paragraph to
have been issued under this section, shall be considered to have been issued under section
409.
(B) Notwithstanding paragraph (3), any regulation applying to the use of the substance that
was in effect on such day and was issued under this section (including any such regulation
issued before the date of the enactment of the Food Quality Protection Act of 1996) is deemed
to have been issued under section 409.
(k) TRANSITIONAL PROVISION.—If, on the day before the date of the enactment of this
subsection, a substance that is a pesticide chemical was, with respect to a particular pesticidal
use of the substance and any resulting pesticide chemical residue in or on a particular food—
(1) regarded by the Administrator or the Secretary as generally recognized as safe for use
within the meaning of the provisions of subsection (a) or section 201(s) as then in effect; or
(2) regarded by the Secretary as a substance described by section 201(s)(4); such a pesticide
chemical residue shall be regarded as exempt from the requirement for a tolerance, as of the
date of enactment of this subsection. The Administrator shall by regulation indicate which
substances are described by this subsection. Any exemption under this subsection may be
modified or revoked as if it had been issued under subsection (c).
(l) HARMONIZATION WITH ACTION UNDER OTHER LAWS.—
(1) COORDINATION WITH FIFRA.—To the extent practicable and consistent with the review
deadlines in subsection (q), in issuing a final rule under this subsection that suspends or
revokes a tolerance or exemption for a pesticide chemical residue in or on food, the
Administrator shall coordinate such action with any related necessary action under the Federal
Insecticide, Fungicide, and Rodenticide Act.
(2) REVOCATION OF TOLERANCE OR EXEMPTION FOLLOWING CANCELLATION OF
ASSOCIATED REGISTRATIONS.—If the Administrator, acting under the Federal Insecticide,
Fungicide, and Rodenticide Act, cancels the registration of each pesticide that contains a
particular pesticide chemical and that is labeled for use on a particular food, or requires that
the registration of each such pesticide be modified to prohibit its use in connection with the
production, storage, or transportation of such food, due in whole or in part to dietary risks to
humans posed by residues of that pesticide chemical on that food, the Administrator shall
revoke any tolerance or exemption that allows the presence of the pesticide chemical, or any
pesticide chemical residue that results from its use, in or on that food. Subsection (e) shall
apply to actions taken under this paragraph. A revocation under this paragraph shall become
effective not later than 180 days after—
(A) the date by which each such cancellation of a registration has become effective; or
(B) the date on which the use of the canceled pesticide becomes unlawful under the terms of
the cancellation, whichever is later.
(3) SUSPENSION OF TOLERANCE OR EXEMPTION FOLLOWING SUSPENSION OF
ASSOCIATED REGISTRATIONS.—
(A) SUSPENSION.—If the Administrator, acting under the Federal Insecticide, Fungicide, and
Rodenticide Act, suspends the use of each registered pesticide that contains a particular
pesticide chemical and that is labeled for use on a particular food, due in whole or in part to
dietary risks to humans posed by residues of that pesticide chemical on that food, the
Administrator shall suspend any tolerance or exemption that allows the presence of the
pesticide chemical, or any pesticide chemical residue that results from its use, in or on that
food. Subsection (e) shall apply to actions taken under this paragraph. A suspension under
this paragraph shall become effective not later than 60 days after the date by which each such
suspension of use has become effective.
(B) EFFECT OF SUSPENSION.—The suspension of a tolerance or exemption under
subparagraph (A) shall be effective as long as the use of each associated registration of a
pesticide is suspended under the Federal Insecticide, Fungicide, and Rodenticide Act. While a
suspension of a tolerance or exemption is effective the tolerance or exemption shall not be
considered to be in effect. If the suspension of use of the pesticide under that Act is terminated,
leaving the registration of the pesticide for such use in effect under that Act, the Administrator
shall rescind any associated suspension of tolerance or exemption.
(4) TOLERANCES FOR UNAVOIDABLE RESIDUES.—In connection with action taken under
paragraph (2) or (3), or with respect to pesticides whose registrations were suspended or
canceled prior to the date of the enactment of this paragraph under the Federal Insecticide,
Fungicide, and Rodenticide Act, if the Administrator determines that a residue of the canceled
or suspended pesticide chemical will unavoidably persist in the environment and thereby be
present in or on a food, the Administrator may establish a tolerance for the pesticide chemical
residue. In establishing such a tolerance, the Administrator shall take into account both the
factors set forth in subsection (b)(2) and the unavoidability of the residue. Subsection (e) shall
apply to the establishment of such tolerance. The Administrator shall review any such
tolerance periodically and modify it as necessary so that it allows no greater level of the
pesticide chemical residue than is unavoidable.
(5) PESTICIDE RESIDUES RESULTING FROM LAWFUL APPLICATION OF
PESTICIDE.—Notwithstanding any other provision of this Act, if a tolerance or exemption for a
pesticide chemical residue in or on a food has been revoked, suspended, or modified under
this section, an article of that food shall not be deemed unsafe solely because of the presence
of such pesticide chemical residue in or on such food if it is shown to the satisfaction of the
Secretary that—
(A) the residue is present as the result of an application or use of a pesticide at a time and in a
manner that was lawful under the Federal Insecticide, Fungicide, and Rodenticide Act; and
(B) the residue does not exceed a level that was authorized at the time of that application or
use to be present on the food under a tolerance, exemption, food additive regulation, or other
sanction then in effect under this Act; unless, in the case of any tolerance or exemption
revoked, suspended, or modified under this subsection or subsection (d) or (e), the
Administrator has issued a determination that consumption of the legally treated food during
the period of its likely availability in commerce will pose an unreasonable dietary risk.
(6) TOLERANCE FOR USE OF PESTICIDES UNDER AN EMERGENCY EXEMPTION.—If
the Administrator grants an exemption under section 18 of the Federal Insecticide, Fungicide,
and Rodenticide Act (7 U.S.C. 136p) for a pesticide chemical, the Administrator shall establish
a tolerance or exemption from the requirement for a tolerance for the pesticide chemical
residue. Such a tolerance or exemption from a tolerance shall have an expiration date. The
Administrator may establish such a tolerance or exemption without providing notice or a period
for comment on the tolerance or exemption. The Administrator shall promulgate regulations
within 365 days after the date of the enactment of this paragraph governing the establishment
of tolerances and exemptions under this paragraph. Such regulations shall be consistent with
the safety standard under subsections (b)(2) and (c)(2) and with section 18 of the Federal
Insecticide, Fungicide, and Rodenticide Act.
(m) 23 FEES.—
(1) AMOUNT.—The Administrator shall by regulation require the payment of such fees as will
in the aggregate, in the judgment of the Administrator, be sufficient over a reasonable term to
provide, equip, and maintain an adequate service for the performance of the Administrator’s
functions under this section. Under the regulations, the performance of the Administrator’s
services or other functions under this section, including—
(A) the acceptance for filing of a petition submitted under subsection (d);
(B) establishing, modifying, leaving in effect, or revoking a tolerance or establishing, modifying,
leaving in effect, or revoking an exemption from the requirement for a tolerance under this
section;
(C) the acceptance for filing of objections under subsection (g); or
(D) the certification and filing in court of a transcript of the proceedings and the record under
subsection (h); may be conditioned upon the payment of such fees. The regulations may
further provide for waiver or refund of fees in whole or in part when in the judgment of the
Administrator such a waiver or refund is equitable and not contrary to the purposes of this
subsection.
(2) DEPOSIT.—All fees collected under paragraph (1) shall be deposited in the Reregistration
and Expedited Processing Fund created by section 4(k) of the Federal Insecticide, Fungicide,
and Rodenticide Act. Such fees shall be available to the Administrator, without fiscal year
limitation, for the performance of the Administrator’s services or functions as specified in
paragraph (1).
(n) NATIONAL UNIFORMITY OF TOLERANCES.—
(1) QUALIFYING PESTICIDE CHEMICAL RESIDUE.—For purposes of this subsection, the
term ‘‘qualifying pesticide chemical residue’’ means a pesticide chemical residue resulting
from the use, in production, processing, or storage of a food, of a pesticide chemical that is an
active ingredient and that—
(A) was first approved for such use in a registration of a pesticide issued under section 3(c)(5)
of the Federal Insecticide, Fungicide, and Rodenticide Act on or after April 25, 1985, on the
basis of data determined by the Administrator to meet all applicable requirements for data
prescribed by regulations in effect under that Act on April 25, 1985; or
(B) was approved for such use in a reregistration eligibility determination issued under section
4(g) of that Act on or after the date of enactment of this subsection.
(2) QUALIFYING FEDERAL DETERMINATION.—For purposes of this subsection, the term
‘‘qualifying Federal determination’’ means a tolerance or exemption from the requirement for a
tolerance for a qualifying pesticide chemical residue that—
(A) is issued under this section after the date of the enactment of this subsection and
determined by the Administrator to meet the standard under subsection (b)(2)(A) (in the case
of a tolerance) or (c)(2) (in the case of an exemption); or
(B)(i) pursuant to subsection (j) is remaining in effect or is deemed to have been issued under
this section, or is regarded under subsection (k) as exempt from the requirement for a
tolerance; and
(ii) is determined by the Administrator to meet the standard under subsection (b)(2)(A) (in the
case of a tolerance) or (c)(2) (in the case of an exemption).
(3) LIMITATION.—The Administrator may make the determination described in paragraph
(2)(B)(ii) only by issuing a rule in accordance with the procedure set forth in subsection (d) or
(e) and only if the Administrator issues a proposed rule and allows a period of not less than 30
days for comment on the proposed rule. Any such rule shall be reviewable in accordance with
subsections (g) and (h).
(4) STATE AUTHORITY.—Except as provided in paragraphs (5), (6), and (8) no State or
political subdivision may establish or enforce any regulatory limit on a qualifying pesticide
chemical residue in or on any food if a qualifying Federal determination applies to the
presence of such pesticide chemical residue in or on such food, unless such State regulatory
limit is identical to such qualifying Federal determination. A State or political subdivision shall
be deemed to establish or enforce a regulatory limit on a pesticide chemical residue in or on a
food if it purports to prohibit or penalize the production, processing, shipping, or other handling
of a food because it contains a pesticide residue (in excess of a prescribed limit).
(5) PETITION PROCEDURE.—
(A) IN GENERAL.—Any State may petition the Administrator for authorization to establish in
such State a regulatory limit on a qualifying pesticide chemical residue in or on any food that is
not identical to the qualifying Federal determination applicable to such qualifying pesticide
chemical residue.
(B) PETITION REQUIREMENTS.—Any petition under subparagraph (A) shall—
(i) satisfy any requirements prescribed, by rule, by the Administrator; and
(ii) be supported by scientific data about the pesticide chemical residue that is the subject of
the petition or about chemically related pesticide chemical residues, data on the consumption
within such State of food bearing the pesticide chemical residue, and data on exposure of
humans within such State to the pesticide chemical residue.
(C) AUTHORIZATION.—The Administrator may, by order, grant the authorization described in
subparagraph (A) if the Administrator determines that the proposed State regulatory limit—
(i) is justified by compelling local conditions; and
(ii) would not cause any food to be a violation of Federal law.
(D) TREATMENT.—In lieu of any action authorized under subparagraph (C), the Administrator
may treat a petition under this paragraph as a petition under subsection (d) to modify or revoke
a tolerance or an exemption. If the Administrator determines to treat a petition under this
paragraph as a petition under subsection (d), the Administrator shall thereafter act on the
petition pursuant to subsection (d).
(E) REVIEW.—Any order of the Administrator granting or denying the authorization described
in subparagraph (A) shall be subject to review in the manner described in subsections (g) and
(h).
(6) URGENT PETITION PROCEDURE.—Any State petition to the Administrator pursuant to
paragraph (5) that demonstrates that consumption of a food containing such pesticide residue
level during the period of the food’s likely availability in the State will pose a significant public
health threat from acute exposure shall be considered an urgent petition. If an order by the
Administrator to grant or deny the requested authorization in an urgent petition is not made
within 30 days of receipt of the petition, the petitioning State may establish and enforce a
temporary regulatory limit on a qualifying pesticide chemical residue in or on the food. The
temporary regulatory limit shall be validated or terminated by the Administrator’s final order on
the petition.
(7) RESIDUES FROM LAWFUL APPLICATION.—No State or political subdivision may
enforce any regulatory limit on the level of a pesticide chemical residue that may appear in or
on any food if, at the time of the application of the pesticide that resulted in such residue, the
sale of such food with such residue level was lawful under this section and under the law of
such State, unless the State demonstrates that consumption of the food containing such
pesticide residue level during the period of the food’s likely availability in the State will pose an
unreasonable dietary risk to the health of persons within such State.
(8) SAVINGS.—Nothing in this Act preempts the authority of any State or political subdivision
to require that a food containing a pesticide chemical residue bear or be the subject of a
warning or other statement relating to the presence of the pesticide chemical residue in or on
such food.
(o) CONSUMER RIGHT TO KNOW.—Not later than 2 years after the date of the enactment of
the Food Quality Protection Act of 1996, and annually thereafter, the Administrator shall, in
consultation with the Secretary of Agriculture and the Secretary of Health and Human Services,
publish in a format understandable to a lay person, and distribute to large retail grocers for
public display (in a manner determined by the grocer), the following information, at a minimum:
(1) A discussion of the risks and benefits of pesticide chemical residues in or on food
purchased by consumers.
(2) A listing of actions taken under subparagraph (B) of subsection (b)(2) that may result in
pesticide chemical residues in or on food that present a yearly or lifetime risk above the risk
allowed under subparagraph (A) of such subsection, and the food on which the pesticide
chemicals producing the residues are used.
(3) Recommendations to consumers for reducing dietary exposure to pesticide chemical
residues in a manner consistent with maintaining a healthy diet, including a list of food that
may reasonably substitute for food listed under paragraph (2).
Nothing 24 in this subsection shall prevent retail grocers from providing additional information.
(p) ESTROGENIC SUBSTANCES SCREENING PROGRAM.—
(1) DEVELOPMENT.—Not later than 2 years after the date of enactment of this section, the
Administrator shall in consultation with the Secretary of Health and Human Services develop a
screening program, using appropriate validated test systems and other scientifically relevant
information, to determine whether certain substances may have an effect in humans that is
similar to an effect produced by a naturally occurring estrogen, or such other endocrine effect
as the Administrator may designate.
(2) IMPLEMENTATION.—Not later than 3 years after the date of enactment of this section,
after obtaining public comment and review of the screening program described in paragraph (1)
by the scientific advisory panel established under section 25(d) of the Federal Insecticide,
Fungicide, and Rodenticide Act or the science advisory board established by section 8 of the
Environmental Research, Development, and Demonstration 25 Act of 1978 (42 U.S.C. 4365),
the Administrator shall implement the program.
(3) SUBSTANCES.—In carrying out the screening program described in paragraph (1), the
Administrator—
(A) shall provide for the testing of all pesticide chemicals; and
(B) may provide for the testing of any other substance that may have an effect that is
cumulative to an effect of a pesticide chemical if the Administrator determines that a
substantial population may be exposed to such substance.
(4) EXEMPTION.—Notwithstanding paragraph (3), the Administrator may, by order, exempt
from the requirements of this section a biologic substance or other substance if the
Administrator determines that the substance is anticipated not to produce any effect in humans
similar to an effect produced by a naturally occurring estrogen.
(5) COLLECTION OF INFORMATION.—
(A) IN GENERAL.—The Administrator shall issue an order to a registrant of a substance for
which testing is required under this subsection, or to a person who manufactures or imports a
substance for which testing is required under this subsection, to conduct testing in accordance
with the screening program described in paragraph (1), and submit information obtained from
the testing to the Administrator, within a reasonable time period that the Administrator
determines is sufficient for the generation of the information.
(B) PROCEDURES.—To the extent practicable the Administrator shall minimize duplicative
testing of the same substance for the same endocrine effect, develop, as appropriate,
procedures for fair and equitable sharing of test costs, and develop, as necessary, procedures
for handling of confidential business information.
(C) FAILURE OF REGISTRANTS TO SUBMIT INFORMATION.—
(i) SUSPENSION.— If a registrant of a substance referred to in paragraph (3)(A) fails to
comply with an order under subparagraph (A) of this paragraph, the Administrator shall issue a
notice of intent to suspend the sale or distribution of the substance by the registrant. Any
suspension proposed under this paragraph shall become final at the end of the 30-day period
beginning on the date that the registrant receives the notice of intent to suspend, unless during
that period a person adversely affected by the notice requests a hearing or the Administrator
determines that the registrant has complied fully with this paragraph.
(ii) HEARING.— If a person requests a hearing under clause (i), the hearing shall be
conducted in accordance with section 554 of title 5, United States Code. The only matter for
resolution at the hearing shall be whether the registrant has failed to comply with an order
under subparagraph (A) of this paragraph. A decision by the Administrator after completion of
a hearing shall be considered to be a final agency action.
(iii) TERMINATION OF SUSPENSIONS.—The Administrator shall terminate a suspension
under this subparagraph issued with respect to a registrant if the Administrator determines that
the registrant has complied fully with this paragraph.
(D) NONCOMPLIANCE BY OTHER PERSONS.—Any person (other than a registrant) who
fails to comply with an order under subparagraph (A) shall be liable for the same penalties and
sanctions as are provided under section 16 of the Toxic Substances Control Act (15 U.S.C.
2601 and following) in the case of a violation referred to in that section. Such penalties and
sanctions shall be assessed and imposed in the same manner as provided in such section 16.
(6) AGENCY ACTION.—In the case of any substance that is found, as a result of testing and
evaluation under this section, to have an endocrine effect on humans, the Administrator shall,
as appropriate, take action under such statutory authority as is available to the Administrator,
including consideration under other sections of this Act, as is necessary to ensure the
protection of public health.
(7) REPORT TO CONGRESS.—Not later than 4 years after the date of enactment of this
section, the Administrator shall prepare and submit to Congress a report containing—
(A) the findings of the Administrator resulting from the screening program described in
paragraph (1);
(B) recommendations for further testing needed to evaluate the impact on human health of the
substances tested under the screening program; and
(C) recommendations for any further actions (including any action described in paragraph (6))
that the Administrator determines are appropriate based on the findings.
(q) SCHEDULE FOR REVIEW.—
(1) IN GENERAL.—The Administrator shall review tolerances and exemptions for pesticide
chemical residues in effect on the day before the date of the enactment of the Food Quality
Protection Act of 1996, as expeditiously as practicable, assuring that—
(A) 33 percent of such tolerances and exemptions are reviewed within 3 years of the date of
enactment of such Act;
(B) 66 percent of such tolerances and exemptions are reviewed within 6 years of the date of
enactment of such Act; and
(C) 100 percent of such tolerances and exemptions are reviewed within 10 years of the date of
enactment of such Act.
In conducting a review of a tolerance or exemption, the Administrator shall determine whether
the tolerance or exemption meets the requirements of subsections 26 (b)(2) or (c)(2) and shall,
by the deadline for the review of the tolerance or exemption, issue a regulation under
subsection (d)(4) or (e)(1) to modify or revoke the tolerance or exemption if the tolerance or
exemption does not meet such requirements.
(2) PRIORITIES.—In determining priorities for reviewing tolerances and exemptions under
paragraph (1), the Administrator shall give priority to the review of the tolerances or
exemptions that appear to pose the greatest risk to public health.
(3) PUBLICATION OF SCHEDULE.—Not later than 12 months after the date of the enactment
of the Food Quality Protection Act of 1996, the Administrator shall publish a schedule for
review of tolerances and exemptions established prior to the date of the enactment of the Food
Quality Protection Act of 1996. The determination of priorities for the review of tolerances and
exemptions pursuant to this subsection is not a rulemaking and shall not be subject to judicial
review, except that failure to take final action pursuant to the schedule established by this
paragraph shall be subject to judicial review.
(r) TEMPORARY TOLERANCE OR EXEMPTION.—The Administrator may, upon the request
of any person who has obtained an experimental permit for a pesticide chemical under the
Federal Insecticide, Fungicide, and Rodenticide Act or upon the Administrator’s own initiative,
establish a temporary tolerance or exemption for the pesticide chemical residue for the uses
covered by the permit. Subsections (b)(2), (c)(2), (d), and (e) shall apply to actions taken under
this subsection.
(s) SAVINGS CLAUSE.—Nothing in this section shall be construed to amend or modify the
provisions of the Toxic Substances Control Act or the Federal Insecticide, Fungicide, and
Rodenticide Act.
FOOD ADDITIVES
Unsafe Food Additives
SEC. 409. [21 U.S.C. 348] (a) A food additive shall, with respect to any particular use or
intended use of such additives, be deemed to be unsafe for the purposes of the application of
clause (2)(C) of section 402(a), unless—
(1) it and its use or intended use conform to the terms of an exemption which is in effect
pursuant to subsection (j) of this section;
(2) there is in effect, and it and its use or intended use are in conformity with, a regulation
issued under this section prescribing the conditions under which such additive may be safely
used; or
(3) in the case of a food additive as defined in this Act that is a food contact substance, there
is—
(A) in effect, and such substance and the use of such substance are in conformity with, a
regulation issued under this section prescribing the conditions under which such additive may
be safely used; or
(B) a notification submitted under subsection (h) that is effective.
While such a regulation relating to a food additive, or such a notification under subsection (h)(1)
relating to a food additive that is a food contact substance, is in effect, and has not been
revoked pursuant to subsection (i), a food shall not, by reason of bearing or containing such a
food additive in accordance with the regulation or notification, be considered adulterated under
section 402(a)(1).
Petition To Establish Safety
(b)(1) Any person may, with respect to any intended use of a food additive, file with the
Secretary a petition proposing the issuance of a regulation prescribing the conditions under
which such additive may be safely used.
(2) Such petition shall, in addition to any explanatory or supporting data, contain—
(A) the name and all pertinent information concerning such food additive, including, where
available, its chemical identity and composition;
(B) a statement of the conditions of the proposed use of such additive, including all directions,
recommendations, and suggestions proposed for the use of such additive, and including
specimens of its proposed labeling;
(C) all relevant data bearing on the physical or other technical effect such additive is intended
to produce, and the quantity of such additive required to produce such effect;
(D) a description of practicable methods for determining the quantity of such additive in or on
food, and any substance formed in or on food, because of its use; and
(E) full reports of investigations made with respect to the safety for use of such additive,
including full information as to the methods and controls used in conducting such
investigations.
(3) Upon request of the Secretary, the petitioner shall furnish (or, if the petitioner is not the
manufacturer of such additive, the petitioner shall have the manufacturer of such additive
furnish, without disclosure to the petitioner), a full description of the methods used in, and the
facilities and controls used for, the production of such additive.
(4) Upon request of the Secretary, the petitioner shall furnish samples of the food additive
involved, or articles used as components thereof, and of the food in or on which the additive is
proposed to be used.
(5) Notice of the regulation proposed by the petitioner shall be published in general terms by
the Secretary within thirty days after filing.
Action on the Petition
(c)(1) The Secretary shall—
(A) by order establish a regulation (whether or not in accord with that proposed by the
petitioner) prescribing, with respect to one or more proposed uses of the food additive involved,
the conditions under which such additive may be safely used (including, but not limited to,
specifications as to the particular food or classes of food in or on which such additive may be
used, the maximum quantity which may be used or permitted to remain in or on such food, the
manner in which such additive may be added to or used in or on such food, and any directions
or other labeling or packaging requirements for such additive deemed necessary by him to
assure the safety of such use), and shall notify the petitioner of such order and the reasons for
such action; or
(B) by order deny the petition, and shall notify the petitioner of such order and of the reasons
for such action.
(2) The order required by paragraph (1) (A) or (B) of this subsection shall be issued within
ninety days after the date of filing of the petition, except that the Secretary may (prior to such
ninetieth day), by written notice to the petitioner, extend such ninety day period to such time
(not more than one hundred and eighty days after the date of filing of the petition) as the
Secretary deems necessary to enable him to study and investigate the petition.
(3) No such regulation shall issue if a fair evaluation of the data before the Secretary—
(A) fails to establish that the proposed use of the food additive, under the conditions of use to
be specified in the regulation, will be safe: Provided, That no additive shall be deemed to be
safe if it is found to induce cancer when ingested by man or animal, or if it is found, after tests
which are appropriate for the evaluation of the safety of food additives, to induce cancer in
man or animal, except that this proviso shall not apply with respect to the use of a substance
as an ingredient of feed for animals which are raised for food production, if the Secretary finds
(i) that, under the conditions of use and feeding specified in proposed labeling and reasonably
certain to be followed in practice, such additive will not adversely affect the animals for which
such feed is intended, and (ii) that no residue of the additive will be found (by methods of
examination prescribed or approved by the Secretary by regulations, which regulations shall
not be subject to subsections (f) and (g)) in any edible portion of such animal after slaughter or
in any food yielded by or derived from the living animal; or
(B) shows that the proposed use of the additive would promote deception of the consumer in
violation of this Act or would otherwise result in adulteration or in misbranding of food within
the meaning of this Act.
(4) If, in the judgment of the Secretary, based upon a fair evaluation of the data before him, a
tolerance limitation is required in order to assure that the proposed use of an additive will be
safe, the Secretary—
(A) shall not fix such tolerance limitation at a level higher than he finds to be reasonably
required to accomplish the physical or other technical effect for which such additive is intended;
and
(B) shall not establish a regulation for such proposed use if he finds upon a fair evaluation of
the data before him that such data do not establish that such use would accomplish the
intended physical or other technical effect.
(5) In determining, for the purposes of this section, whether a proposed use of a food additive
is safe, the Secretary shall consider among other relevant factors—
(A) the probable consumption of the additive and of any substance formed in or on food
because of the use of the additive;
(B) the cumulative effect of such additive in the diet of man or animals, taking into account any
chemically or pharmacologically related substance or substances in such diet; and
(C) safety factors which in the opinion of experts qualified by scientific training and experience
to evaluate the safety of food additives are generally recognized as appropriate for the use of
animal experimentation data.
Regulation Issued on Secretary's Initiative
(d) The Secretary may at any time, upon his own initiative, propose the issuance of a
regulation prescribing, with respect to any particular use of a food additive, the conditions
under which such additive may be safely used, and the reasons therefor. After the thirtieth day
following publication of such a proposal, the Secretary may by order establish a regulation
based upon the proposal.
Publication and Effective Date of Orders
(e) Any order, including any regulation established by such order, issued under subsection (c)
or (d) of this section, shall be published and shall be effective upon publication, but the
Secretary may stay such effectiveness if, after issuance of such order, a hearing is sought with
respect to such order pursuant to subsection (f).
Objections and Public Hearing
(f)(1) Within thirty days after publication of an order made pursuant to subsection (c) or (d) of
this section, any person adversely affected by such an order may file objections thereto with
the Secretary, specifying with particularity the provisions of the order deemed objectionable,
stating reasonable grounds therefor, and requesting a public hearing upon such objections.
The Secretary shall, after due notice, as promptly as possible hold such public hearing for the
purpose of receiving evidence relevant and material to the issues raised by such objections.
As soon as practicable after completion of the hearing, the Secretary shall by order act upon
such objections and make such order public.
(2) Such order shall be based upon a fair evaluation of the entire record at such hearing, and
shall include a statement setting forth in detail the findings and conclusions upon which the
order is based.
(3) The Secretary shall specify in the order the date on which it shall take effect, except that it
shall not be made to take effect prior to the ninetieth day after its publication, unless the
Secretary finds that emergency conditions exist necessitating an earlier effective date, in
which event the Secretary shall specify in the order his findings as to such conditions.
Judicial Review
(g)(1) In a case of actual controversy as to the validity of any order issued under subsection (f),
including any order thereunder with respect to amendment or repeal of a regulation issued
under this section, any person who will be adversely affected by such order may obtain judicial
review by filing in the United States Court of Appeals for the circuit wherein such person
resides or has his principal place of business, or in the United States Court of Appeals for the
District of Columbia Circuit, within sixty days after the entry of such order, a petition praying
that the order be set aside in whole or in part.
(2) A copy of such petition shall be forthwith transmitted by the clerk of the court to the
Secretary, or any officer designated by him for that purpose, and thereupon the Secretary shall
file in the court the record of the proceedings on which he based his order, as provided in
section 2112 of title 28, United States Code. Upon the filing of such petition the court shall
have jurisdiction, which upon the filing of the record with it shall be exclusive, to affirm or set
aside the order complained of in whole or in part. Until the filing of the record the Secretary
may modify or set aside his order. The findings of the Secretary with respect to questions of
fact shall be sustained if based upon a fair evaluation of the entire record at such hearing.
(3) The court, on such judicial review, shall not sustain the order of the Secretary if he failed to
comply with any requirement imposed on him by subsection (f)(2) of this section.
(4) If application is made to the court for leave to adduce additional evidence, the court may
order such additional evidence to be taken before the Secretary and to be adduced upon the
hearing in such manner and upon such terms and conditions as to the court may seem proper,
if such evidence is material and there were reasonable grounds for failure to adduce such
evidence in the proceedings below. The Secretary may modify his findings as to the facts and
order by reason of the additional evidence so taken, and shall file with the court such modified
findings and order.
(5) The judgment of the court affirming or setting aside, in whole or in part, any order under this
section shall be final, subject to review by the Supreme Court of the United States upon
certiorari or certification as provided in section 1254 of title 28 of the United States Code. The
commencement of proceedings under this section shall not, unless specifically ordered by the
court to the contrary, operate as a stay of an order.
Notification Relating to a Food Contact Substance
(h)(1) Subject to such regulations as may be promulgated under paragraph (3), a
manufacturer or supplier of a food contact substance may, at least 120 days prior to the
introduction or delivery for introduction into interstate commerce of the food contact substance,
notify the Secretary of the identity and intended use of the food contact substance, and of the
determination of the manufacturer or supplier that the intended use of such food contact
substance is safe under the standard described in subsection (c)(3)(A). The notification shall
contain the information that forms the basis of the determination and all information required to
be submitted by regulations promulgated by the Secretary.
(2)(A) A notification submitted under paragraph (1) shall become effective 120 days after the
date of receipt by the Secretary and the food contact substance may be introduced or
delivered for introduction into interstate commerce, unless the Secretary makes a
determination within the 120-day period that, based on the data and information before the
Secretary, such use of the food contact substance has not been shown to be safe under the
standard described in subsection (c)(3)(A), and informs the manufacturer or supplier of such
determination.
(B) A decision by the Secretary to object to a notification shall constitute final agency action
subject to judicial review.
(C) In this paragraph, the term ‘‘food contact substance’’ means the substance that is the
subject of a notification submitted under paragraph (1), and does not include a similar or
identical substance manufactured or prepared by a person other than the manufacturer
identified in the notification.
(3)(A) The process in this subsection shall be utilized for authorizing the marketing of a food
contact substance except where the Secretary determines that submission and review of a
petition under subsection (b) is necessary to provide adequate assurance of safety, or where
the Secretary and any manufacturer or supplier agree that such manufacturer or supplier may
submit a petition under subsection (b).
(B) The Secretary is authorized to promulgate regulations to identify the circumstances in
which a petition shall be filed under subsection (b), and shall consider criteria such as the
probable consumption of such food contact substance and potential toxicity of the food contact
substance in determining the circumstances in which a petition shall be filed under subsection
(b).
(4) The Secretary shall keep confidential any information provided in a notification under
paragraph (1) for 120 days after receipt by the Secretary of the notification. After the expiration
of such 120 days, the information shall be available to any interested party except for any
matter in the notification that is a trade secret or confidential commercial information.
(5)(A)(i) Except as provided in clause (ii), the notification program established under this
subsection shall not operate in any fiscal year unless—
(I) an appropriation equal to or exceeding the applicable amount under clause (iv) is made for
such fiscal year for carrying out such program in such fiscal year; and
(II) the Secretary certifies that the amount appropriated for such fiscal year for the Center for
Food Safety and Applied Nutrition of the Food and Drug Administration (exclusive of the
appropriation referred to in subclause (I)) equals or exceeds the amount appropriated for the
Center for fiscal year 1997, excluding any amount appropriated for new programs.
(ii) The Secretary shall, not later than April 1, 1999, begin accepting and reviewing notifications
submitted under the notification program established under this subsection if—
(I) an appropriation equal to or exceeding the applicable amount under clause (iii) is made for
the last six months of fiscal year 1999 for carrying out such program during such period; and
(II) the Secretary certifies that the amount appropriated for such period for the Center for Food
Safety and Applied Nutrition of the Food and Drug Administration (exclusive of the
appropriation referred to in subclause (I)) equals or exceeds an amount equivalent to one-half
the amount appropriated for the Center for fiscal year 1997, excluding any amount
appropriated for new programs.
(iii) For the last six months of fiscal year 1999, the applicable amount under this clause is
$1,500,000, or the amount specified in the budget request of the President for the six-month
period involved for carrying out the notification program in fiscal year 1999, whichever is less.
(iv) For fiscal year 2000 and subsequent fiscal years, the applicable amount under this clause
is $3,000,000, or the amount specified in the budget request of the President for the fiscal year
involved for carrying out the notification program under this subsection, whichever is less.
(B) For purposes of carrying out the notification program under this subsection, there are
authorized to be appropriated such sums as may be necessary for each of the fiscal years
1999 through fiscal year 2003, except that such authorization of appropriations is not effective
for a fiscal year for any amount that is less than the applicable amount under clause (iii) or (iv)
of subparagraph (A), whichever is applicable.
(C) Not later than April 1 of fiscal year 1998 and February 1 of each subsequent fiscal year, the
Secretary shall submit a report to the Committees on Appropriations of the House of
Representatives and the Senate, the Committee on Commerce of the House of
Representatives, and the Committee on Labor and Human Resources of the Senate that
provides an estimate of the Secretary of the costs of carrying out the notification program
established under this subsection for the next fiscal year.
(6) In this section, the term ‘‘food contact substance’’ means any substance intended for use
as a component of materials used in manufacturing, packing, packaging, transporting, or
holding food if such use is not intended to have any technical effect in such food.
Amendment or Repeal of Regulations
(i) The Secretary shall by regulation prescribe the procedure by which regulations under the
foregoing provisions of this section may be amended or repealed, and such procedure shall
conform to the procedure provided in this section for the promulgation of such regulations. The
Secretary shall by regulation prescribe the procedure by which the Secretary may deem a
notification under subsection (h) to no longer be effective.
Exemptions for Investigational Use
(j) Without regard to subsections (b) to (i), inclusive, of this section, the Secretary shall by
regulation provide for exempting from the requirements of this section any food additive, and
any food bearing or containing such additive, intended solely for investigational use by
qualified experts when in his opinion such exemption is consistent with the public health.
BOTTLED DRINKING WATER STANDARDS
SEC. 410. [21 U.S.C. 349] (a) Except as provided in subsection (b), whenever the
Administrator of the Environmental Protection Agency prescribes interim or revised national
primary drinking water regulations under section 1412 of the Public Health Service Act, the
Secretary shall consult with the Administrator and within 180 days after the promulgation of
such drinking water regulations either promulgate amendments to regulations under this
chapter applicable to bottled drinking water or publish in the Federal Register his reasons for
not making such amendments.
(b)(1) Not later than 180 days before the effective date of a national primary drinking water
regulation promulgated by the Administrator of the Environmental Protection Agency for a
contaminant under section 1412 of the Safe Drinking Water Act (42 U.S.C. 300g–1), the
Secretary shall promulgate a standard of quality regulation under this subsection for that
contaminant in bottled water or make a finding that such a regulation is not necessary to
protect the public health because the contaminant is contained in water in public water
systems (as defined under section 1401(4) of such Act (42 U.S.C. 300f(4))) but not in water
used for bottled drinking water. The effective date for any such standard of quality regulation
shall be the same as the effective date for such national primary drinking water regulation,
except for any standard of quality of regulation promulgated by the Secretary before the date
of enactment of the Safe Drinking Water Act Amendments of 1996 for which (as of such date
of enactment) an effective date had not been established. In the case of a standard of quality
regulation to which such exception applies, the Secretary shall promulgate monitoring
requirements for the contaminants covered by the regulation not later than 2 years after such
date of enactment.
(2) A regulation issued by the Secretary as provided in this subsection shall include any
monitoring requirements that the Secretary determines appropriate for bottled water.
(3) A regulation issued by the Secretary as provided in this subsection shall require the
following:
(A) In the case of contaminants for which a maximum contaminant level is established in a
national primary drinking water regulation under section 1412 of the Safe Drinking Water Act
(42 U.S.C. 300g–1), the regulation under this subsection shall establish a maximum
contaminant level for the contaminant in bottled water which is no less stringent than the
maximum contaminant level provided in the national primary drinking water regulation.
(B) In the case of contaminants for which a treatment technique is established in a national
primary drinking water regulation under section 1412 of the Safe Drinking Water Act (42 U.S.C.
300g–1), the regulation under this subsection shall require that bottled water be subject to
requirements no less protective of the public health than those applicable to water provided by
public water systems using the treatment technique required by the national primary drinking
water regulation.
(4)(A) If the Secretary does not promulgate a regulation under this subsection within the period
described in paragraph (1), the national primary drinking water regulation referred to in
paragraph (1) shall be considered, as of the date on which the Secretary is required to
establish a regulation under paragraph (1), as the regulation applicable under this subsection
to bottled water.
(B) In the case of a national primary drinking water regulation that pursuant to subparagraph
(A) is considered to be a standard of quality regulation, the Secretary shall, not later than the
applicable date referred to in such subparagraph, publish in the Federal Register a notice—
(i) specifying the contents of such regulation, including monitoring requirements; and
(ii) providing that for purposes of this paragraph the effective date for such regulation is the
same as the effective date for the regulation for purposes of the Safe Drinking Water Act (or, if
the exception under paragraph (1) applies to the regulation, that the effective date for the
regulation is not later than 2 years and 180 days after the date of enactment of the Safe
Drinking Water Act Amendments of 1996).
VITAMINS AND MINERALS
SEC. 411. [21 U.S.C. 350] (a)(1) Except as provided in paragraph (2)—
(A) the Secretary may not establish, under section 201(n), 401, or 403, maximum limits on the
potency of any synthetic or natural vitamin or mineral within a food to which this section
applies;
(B) the Secretary may not classify any natural or synthetic vitamin or mineral (or combination
thereof) as a drug solely because it exceeds the level of potency which the Secretary
determines is nutritionally rational or useful;
(C) the Secretary may not limit, under section 201(n), 401, or 403, the combination or number
of any synthetic or natural—
(i) vitamin,
(ii) mineral, or
(iii) other ingredient of food,
within a food to which this section applies.
(2) Paragraph (1) shall not apply in the case of a vitamin, mineral, other ingredient of food, or
food, which is represented for use by individuals in the treatment or management of specific
diseases or disorders, by children, or by pregnant or lactating women. For purposes of this
subparagraph 27 , the term "children" means individuals who are under the age of twelve
years.
(b)(1) A food to which this section applies shall not be deemed under section 403 to be
misbranded solely because its label bears, in accordance with section 403(i)(2), all the
ingredients in the food or its advertising contains references to ingredients in the food which
are not vitamins or minerals.
(2) The labeling for any food to which this section applies may not list its ingredients which are
not dietary supplement ingredients described in section 201(ff) (i) except as a part of a list of all
the ingredients of such food, and (ii) unless such ingredients are listed in accordance with
applicable regulations under section 403. To the extent that compliance with clause (i) of this
subparagraph is impracticable or results in deception or unfair competition, exemptions shall
be established by regulations promulgated by the Secretary.
(c)(1) For purposes of this section, the term ‘‘food to which this section applies’’ means a food
for humans which is a food for special dietary use—
(A) which is or contains any natural or synthetic vitamin or mineral, and
(B) which—
(i) is intended for ingestion in tablet, capsule, powder, softgel, gelcap, or liquid form, or
(ii) if not intended for ingestion in such a form, is not represented as conventional food and is
not represented for use as a sole item of a meal or of the diet.
(2) For purposes of paragraph (1)(B)(i), a food shall be considered as intended for ingestion in
liquid form only if it is formulated in a fluid carrier and it is intended for ingestion in daily
quantities measured in drops or similar small units of measure.
(3) For purposes of paragraph (1) and of section 403 (j) insofar as that section is applicable to
food to which this section applies, the term ‘‘special dietary use’’ as applied to food used by
man means a particular use for which a food purports or is represented to be used, including
but not limited to the following:
(A) Supplying a special dietary need that exists by reason of a physical, physiological,
pathological, or other condition, including but not limited to the condition of disease,
convalescence, pregnancy, lactation, infancy, allergic hypersensitivity to food, underweight,
overweight, or the need to control the intake of sodium.
(B) Supplying a vitamin, mineral, or other ingredient for use by man to supplement his diet by
increasing the total dietary intake.
(C) Supplying a special dietary need by reason of being a food for use as the sole item of the
diet.
REQUIREMENTS FOR INFANT FORMULAS
SEC. 412. [21 U.S.C. 350a] (a) An infant formula, including an infant formula powder, shall be
deemed to be adulterated if—
(1) such infant formula does not provide nutrients as required by subsection (i),
(2) such infant formula does not meet the quality factor requirements prescribed by the
Secretary under subsection (b)(1), or
(3) the processing of such infant formula is not in compliance with the good manufacturing
practices and the quality control procedures prescribed by the Secretary under subsection
(b)(2).
(b)(1) The Secretary shall by regulation establish requirements for quality factors for infant
formulas to the extent possible consistent with current scientific knowledge, including quality
factor requirements for the nutrients required by subsection (i).
(2)(A) The Secretary shall by regulation establish good manufacturing practices for infant
formulas, including quality control procedures that the Secretary determines are necessary to
assure that an infant formula provides nutrients in accordance with this subsection and
subsection (i) and is manufactured in a manner designed to prevent adulteration of the infant
formula.
(B) The good manufacturing practices and quality control procedures prescribed by the
Secretary under subparagraph (A) shall include requirements for—
(i) the testing, in accordance with paragraph (3) and by the manufacturer of an infant formula
or an agent of such manufacturer, of each batch of infant formula for each nutrient required by
subsection (i) before the distribution of such batch,
(ii) regularly scheduled testing, by the manufacturer of an infant formula or an agent of such
manufacturer, of samples of infant formulas during the shelf life of such formulas to ensure that
such formulas are in compliance with this section,
(iii) in-process controls including, where necessary, testing required by good manufacturing
practices designed to prevent adulteration of each batch of infant formula, and
(iv) the conduct by the manufacturer of an infant formula or an agent of such manufacturer of
regularly scheduled audits to determine that such manufacturer has complied with the
regulations prescribed under subparagraph (A).
In prescribing requirements for audits under clause (iv), the Secretary shall provide that such
audits be conducted by appropriately trained individuals who do not have any direct
responsibility for the manufacture or production of infant formula.
(3)(A) At the final product stage, each batch of infant formula shall be tested for vitamin A,
vitamin B1, vitamin C, and vitamin E to ensure that such infant formula is in compliance with
the requirements of this subsection and subsection (i) relating to such vitamins.
(B) Each nutrient premix used in the manufacture of an infant formula shall be tested for each
relied upon nutrient required by subsection (i) which is contained in such premix to ensure that
such premix is in compliance with its specifications or certifications by a premix supplier.
(C) During the manufacturing process or at the final product stage and before distribution of an
infant formula, an infant formula shall be tested for all nutrients required to be included in such
formula by subsection (i) for which testing has not been conducted pursuant to subparagraph
(A) or (B). Testing under this subparagraph shall be conducted to—
(i) ensure that each batch of such infant formula is in compliance with the requirements of
subsection (i) relating to such nutrients, and
(ii) confirm that nutrients contained in any nutrient premix used in such infant formula are
present in each batch of such infant formula in the proper concentration.
(D) If the Secretary adds a nutrient to the list of nutrients in the table in subsection (i), the
Secretary shall by regulation require that the manufacturer of an infant formula test each batch
of such formula for such new nutrient in accordance with subparagraph (A), (B), or (C).
(E) For purposes of this paragraph, the term ‘‘final product stage’’ means the point in the
manufacturing process, before distribution of an infant formula, at which an infant formula is
homogenous and is not subject to further degradation.
(4)(A) The Secretary shall by regulation establish requirements respecting the retention of
records. Such requirements shall provide for—
(i) the retention of all records necessary to demonstrate compliance with the good
manufacturing practices and quality control procedures prescribed by the Secretary under
paragraph (2), including records containing the results of all testing required under paragraph
(2)(B),
(ii) the retention of all certifications or guarantees of analysis by premix suppliers,
(iii) the retention by a premix supplier of all records necessary to confirm the accuracy of all
premix certifications and guarantees of analysis,
(iv) the retention of—
(I) all records pertaining to the microbiological quality and purity of raw materials used in infant
formula powder and in finished infant formula, and
(II) all records pertaining to food packaging materials which show that such materials do not
cause an infant formula to be adulterated within the meaning of section 402(a)(2)(C),
(v) the retention of all records of the results of regularly scheduled audits conducted pursuant
to the requirements prescribed by the Secretary under paragraph (2)(B)(iv), and
(vi) the retention of all complaints and the maintenance of files with respect to, and the review
of, complaints concerning infant formulas which may reveal the possible existence of a hazard
to health.
(B)(i) Records required under subparagraph (A) with respect to an infant formula shall be
retained for at least one year after the expiration of the shelf life of such infant formula. Except
as provided in clause (ii), such records shall be made available to the Secretary for review and
duplication upon request of the Secretary.
(ii) A manufacturer need only provide written assurances to the Secretary that the regularly
scheduled audits required by paragraph (2)(B)(iv) are being conducted by the manufacturer,
and need not make available to the Secretary the actual written reports of such audits.
(c)(1) No person shall introduce or deliver for introduction into interstate commerce any new
infant formula unless—
(A) such person has, before introducing such new infant formula, or delivering such new infant
formula for introduction, into interstate commerce, registered with the Secretary the name of
such person, the place of business of such person, and all establishments at which such
person intends to manufacture such new infant formula, and
(B) such person has at least 90 days before marketing such new infant formula, made the
submission to the Secretary required by subsection (c)(1).
(2) For purposes of paragraph (1), the term ‘‘new infant formula’’ includes—
(A) an infant formula manufactured by a person which has not previously manufactured an
infant formula, and
(B) an infant formula manufactured by a person which has previously manufactured infant
formula and in which there is a major change, in processing or formulation, from a current or
any previous formulation produced by such manufacturer.
For purposes of this paragraph, the term "major change" has the meaning given to such term
in section 106.30(c)(2) of title 21, Code of Federal Regulations (as in effect on August 1, 1986),
and guidelines issued thereunder.
(d)(1) A person shall, with respect to any infant formula subject to subsection (c), make a
submission to the Secretary which shall include—
(A) the quantitative formulation of the infant formula,
(B) a description of any reformulation of the formula or change in processing of the infant
formula,
(C) assurances that the infant formula will not be marketed unless it meets the requirements of
subsections (b)(1) and (i), as demonstrated by the testing required under subsection (b)(3),
and
(D) assurances that the processing of the infant formula complies with subsection (b)(2).
(2) After the first production of an infant formula subject to subsection (c), and before the
introduction into interstate commerce of such formula, the manufacturer of such formula shall
submit to the Secretary, in such form as may be prescribed by the Secretary, a written
verification which summarizes test results and records demonstrating that such formula
complies with the requirements of subsections (b)(1), (b)(2)(A), (b)(2)(B)(i), (b)(2)(B)(iii),
(b)(3)(A), (b)(3)(C), and (i).
(3) If the manufacturer of an infant formula for commercial or charitable distribution for human
consumption determines that a change in the formulation of the formula or a change in the
processing of the formula may affect whether the formula is adulterated under subsection (a),
the manufacturer shall, before the first processing of such formula, make the submission to the
Secretary required by paragraph (1).
(e)(1) If the manufacturer of an infant formula has knowledge which reasonably supports the
conclusion that an infant formula which has been processed by the manufacturer and which
has left an establishment subject to the control of the manufacturer—
(A) may not provide the nutrients required by subsection (i), or
(B) may be otherwise adulterated or misbranded, the manufacturer shall promptly notify the
Secretary of such knowledge. If the Secretary determines that the infant formula presents a
risk to human health, the manufacturer shall immediately take all actions necessary to recall
shipments of such infant formula from all wholesale and retail establishments, consistent with
recall regulations and guidelines issued by the Secretary.
(2) For purposes of paragraph (1), the term ‘‘knowledge’’ as applied to a manufacturer means
(A) the actual knowledge that the manufacturer had, or (B) the knowledge which a reasonable
person would have had under like circumstances or which would have been obtained upon the
exercise of due care.
(f)(1) If a recall of infant formula is begun by a manufacturer, the recall shall be carried out in
accordance with such requirements as the Secretary shall prescribe under paragraph (2)
and—
(A) the Secretary shall, not later than the 15th day after the beginning of such recall and at
least once every 15 days thereafter until the recall is terminated, review the actions taken
under the recall to determine whether the recall meets the requirements prescribed under
paragraph (2), and
(B) the manufacturer shall, not later than the 14th day after the beginning of such recall and at
least once every 14 days thereafter until the recall is terminated, report to the Secretary the
actions taken to implement the recall.
(2) The Secretary shall by regulation prescribe the scope and extent of recalls of infant
formulas necessary and appropriate for the degree of risks to human health presented by the
formula subject to the recall.
(3) The Secretary shall by regulation require each manufacturer of an infant formula who
begins a recall of such formula because of a risk to human health to request each retail
establishment at which such formula is sold or available for sale to post at the point of
purchase of such formula a notice of such recall at such establishment for such time that the
Secretary determines necessary to inform the public of such recall.
(g)(1) Each manufacturer of an infant formula shall make and retain such records respecting
the distribution of the infant formula through any establishment owned or operated by such
manufacturer as may be necessary to effect and monitor recalls of the formula. Such records
shall be retained for at least one year after the expiration of the shelf life of the infant formula.
(2) To the extent that the Secretary determines that records are not being made or maintained
in accordance with paragraph (1), the Secretary may by regulation prescribe the records
required to be made under paragraph (1) and requirements respecting the retention of such
records under such paragraph. Such regulations shall take effect on such date as the
Secretary prescribes but not sooner than the 180th day after the date such regulations are
promulgated. Such regulations shall apply only with respect to distributions of infant formulas
made after such effective date.
(h)(1) Any infant formula which is represented and labeled for use by an infant—
(A) who has an inborn error of metabolism or a low birth weight, or
(B) who otherwise has an unusual medical or dietary problem,
is exempt from the requirements of subsections (a), (b), and (c). The manufacturer of an infant
formula exempt under this paragraph shall, in the case of the exempt formula, be required to
provide the notice required by subsection (e)(1) only with respect to adulteration or
misbranding described in subsection (e)(1)(B) and to comply with the regulations prescribed
by the Secretary under paragraph (2).
(2) The Secretary may by regulation establish terms and conditions for the exemption of an
infant formula from the requirements of subsections (a), (b), and (c). An exemption of an infant
formula under paragraph (1) may be withdrawn by the Secretary if such formula is not in
compliance with applicable terms and conditions prescribed under this paragraph.
(i)(1) An infant formula shall contain nutrients in accordance with the table set out in this
subsection or, if revised by the Secretary under paragraph (2), as so revised.
(2) The Secretary may by regulation—
(A) revise the list of nutrients in the table in this subsection, and
(B) revise the required level for any nutrient required by the table.
NUTRIENTS
Nutrient Minimum 1 Maximum 1
Protein (gm) 1.8 2 4.5.
Fat:
gm 3.3 6.0.
percent cal 30.0 54.0.
Essential fatty acids
(linoleate):
percent cal 2.7
mg 300.0
Vitamins:
A (IU) 250.0 (75 µg) 3 750.0 (225 µg) 3
D (IU) 40.0 100.0.
K (µg) 4.0
E (IU) 0.7 (with 0.7 IU/gm
linoleic acid).
C (ascorbic acid) (mg) 8.0
B1 (thiamine) (µg) 40.0
B2 (riboflavin) (µg) 60.0
B6 (pyridoxine) (µg) 35.0 (with 15 µg/gm of
protein in formula).
B12 (µg) 0.15
Niacin (µg) 250.0
Folic acid (µg) 4.0
Pantothenic acid (µg) 300.0
Biotin (µg) 1.5 4
Choline (mg) 7.0 4
Inositol (mg) 4.0 4
Minerals:
Calcium (mg) 50.0 5
Phosphorus (mg) 25.0 5
Magnesium (mg) 6.0
Iron (mg) 0.15
Iodine (µg) 5.0
Zinc (mg) 0.5
Copper (µg) 60.0
Manganese (µg) 5.0
Sodium (mg) 20.0 60.0.
Potassium (mg) 80.0 200.0.
Chloride (mg) 55.0 150.0.
__________________________________________________________________
1 Stated per 100 kilocalories.
2 The source of protein shall be at least nutritionally equivalent to casein.
3 Retinol equivalents.
4 Required to be included in this amount only in formulas which are not milk-based.
5 Calcium to phosphorus ratio must be no less than 1.1 nor more than 2.0.
NEW DIETARY INGREDIENTS
SEC. 413 . [21 U.S.C. 350b] (a) IN GENERAL.—A dietary supplement which contains a new
dietary ingredient shall be deemed adulterated under section 402(f) unless it meets one of the
following requirements:
(1) The dietary supplement contains only dietary ingredients which have been present in the
food supply as an article used for food in a form in which the food has not been chemically
altered.
(2) There is a history of use or other evidence of safety establishing that the dietary ingredient
when used under the conditions recommended or suggested in the labeling of the dietary
supplement will reasonably be expected to be safe and, at least 75 days before being
introduced or delivered for introduction into interstate commerce, the manufacturer or
distributor of the dietary ingredient or dietary supplement provides the Secretary with
information, including any citation to published articles, which is the basis on which the
manufacturer or distributor has concluded that a dietary supplement containing such dietary
ingredient will reasonably be expected to be safe.
The Secretary shall keep confidential any information provided under paragraph (2) for 90
days following its receipt. After the expiration of such 90 days, the Secretary shall place such
information on public display, except matters in the information which are trade secrets or
otherwise confidential, commercial information.
(b) PETITION.—Any person may file with the Secretary a petition proposing the issuance of an
order prescribing the conditions under which a new dietary ingredient under its intended
conditions of use will reasonably be expected to be safe. The Secretary shall make a decision
on such petition within 180 days of the date the petition is filed with the Secretary. For
purposes of chapter 7 of title 5, United States Code, the decision of the Secretary shall be
considered final agency action.
(c) DEFINITION.—For purposes of this section, the term ‘‘new dietary ingredient’’ means a
dietary ingredient that was not marketed in the United States before October 15, 1994 and
does not include any dietary ingredient which was marketed in the United States before
October 15, 1994.
SEC. 414.[21 USC 350c] MAINTENANCE AND INSPECTION OF RECORDS
(a) RECORDS INSPECTION. — If the Secretary has a reasonable belief that an article of food
is adulterated and presents a threat of serious adverse health consequences or death to
humans or animals, each person (excluding farms and restaurants) who manufactures,
processes, packs, distributes, receives, holds, or imports such article shall, at the request of an
officer or employee duly designated by the Secretary, permit such officer or employee, upon
presentation of appropriate credentials and a written notice to such person, at reasonable
times and within reasonable limits and in a reasonable manner, to have access to and copy all
records relating to such article that are needed to assist the Secretary in determining whether
the food is adulterated and presents a threat of serious adverse health consequences or death
to humans or animals. The requirement under the preceding sentence applies to all records
relating to the manufacture, processing, packing, distribution, receipt, holding, or importation of
such article maintained by or on behalf of such person in any format (including paper and
electronic formats) and at any location.
(b) REGULATIONS CONCERNING RECORDKEEPING.—The Secretary, in consultation and
coordination, as appropriate, with other Federal departments and agencies with
responsibilities for regulating food safety, may by regulation establish requirements regarding
the establishment and maintenance, for not longer than two years, of records by persons
(excluding farms and restaurants) who manufacture, process, pack, transport, distribute,
receive, hold, or import food, which records are needed by the Secretary for inspection to allow
the Secretary to identify the immediate previous sources and the immediate subsequent
recipients of food, including its packaging, in order to address credible threats of serious
adverse health consequences or death to humans or animals. The Secretary shall take into
account the size of a business in promulgating regulations under this section.
(c) Protection of Sensitive Information.—The Secretary shall take appropriate measures to
ensure that there are in effect effective procedures to prevent the unauthorized disclosure of
any trade secret or confidential information that is obtained by the Secretary pursuant to this
section.
(d) Limitations.—This section shall not be construed--
(1) to limit the authority of the Secretary to inspect records or to require establishment and
maintenance of records under any other provision of this Act;
(2) to authorize the Secretary to impose any requirements with respect to a food to the extent
that it is within the exclusive jurisdiction of the Secretary of Agriculture pursuant to the Federal
Meat Inspection Act (21 U.S.C. 601 et seq.), the Poultry Products Inspection Act (21 U.S.C.
451 et seq.), or the Egg Products Inspection Act (21 U.S.C. 1031 et seq.);
(3) to have any legal effect on section 552 of title 5, United States Code, or section 1905 of title
18, United States Code; or
(4) to extend to recipes for food, financial data, pricing data, personnel data, research data, or
sales data (other than shipment data regarding sales).
SEC. 415 . [21 USC 350d].REGISTRATION OF FOOD FACILITIES
(a) Registration.—
(1) Regulations.— In general.--The Secretary shall by regulation require that any facility
engaged in manufacturing, processing, packing, or holding food for consumption in the United
States be registered with the Secretary. To be registered--
(A) for a domestic facility, the owner, operator, or agent in charge of the facility shall submit a
registration to the Secretary; and
(B) for a foreign facility, the owner, operator, or agent in charge of the facility shall submit a
registration to the Secretary and shall include with the registration the name of the United
States agent for the facility.
(2) Registration.—An entity (referred to in this section as the `registrant') shall submit a
registration under paragraph (1) to the Secretary containing information necessary to notify the
Secretary of the name and address of each facility at which, and all trade names under which,
the registrant conducts business and, when determined necessary by the Secretary through
guidance, the general food category (as identified under section 170.3 of title 21, Code of
Federal Regulations) of any food manufactured, processed, packed, or held at such facility.
The registrant shall notify the Secretary in a timely manner of changes to such information.
(3) Notification.—Upon receipt of a completed registration described in paragraph (1), the
Secretary shall notify the registrant of the receipt of such registration and assign a registration
number to each registered facility.
(4) Records.—The Secretary shall compile and maintain an up-to-date list of facilities that are
registered under this section. Such list and any registration documents submitted pursuant to
this subsection shall not be subject to disclosure under section 552 of title 5, United States
Code. Information derived from such list or registration documents shall not be subject to
disclosure under section 552 of title 5, United States Code, to the extent that it discloses the
identity or location of a specific registered person.
(b) Facility.—For purposes of this section:
(1) The term `facility' includes any factory, warehouse, or establishment (including a factory,
warehouse, or establishment of an importer) that manufactures, processes, packs, or holds
food. Such term does not include farms; restaurants; other retail food establishments; nonprofit
food establishments in which food is prepared for or served directly to the consumer; or fishing
vessels (except such vessels engaged in processing as defined in section 123.3(k) of title 21,
Code of Federal Regulations).
(2) The term `domestic facility' means a facility located in any of the States or Territories.
(3)(A) The term `foreign facility' means a facility that manufacturers, processes, packs, or
holds food, but only if food from such facility is exported to the United States without further
processing or packaging outside the United States.
(B) A food may not be considered to have undergone further processing or packaging for
purposes of subparagraph (A) solely on the basis that labeling was added or that any similar
activity of a de minimis nature was carried out with respect to the food.
(c) Rule of Construction.—Nothing in this section shall be construed to authorize the Secretary
to require an application, review, or licensing process.
Sec. 416 [21 USC § 350e] SANITARY TRANSPORTATION PRACTICES
(a) Definitions. In this section:
(1) Bulk vehicle. The term "bulk vehicle" includes a tank truck, hopper truck, rail tank car,
hopper car, cargo tank, portable tank, freight container, or hopper bin, and any other vehicle in
which food is shipped in bulk, with the food coming into direct contact with the vehicle.
(2) Transportation. The term "transportation" means any movement in commerce by motor
vehicle or rail vehicle.
(b) Regulations. The Secretary shall by regulation require shippers, carriers by motor vehicle
or rail vehicle, receivers, and other persons engaged in the transportation of food to use
sanitary transportation practices prescribed by the Secretary to ensure that food is not
transported under conditions that may render the food adulterated.
(c) Contents. The regulations under subsection (b) shall--
(1) prescribe such practices as the Secretary determines to be appropriate relating to--
(A) sanitation;
(B) packaging, isolation, and other protective measures;
(C) limitations on the use of vehicles;
(D) information to be disclosed--
(i) to a carrier by a person arranging for the transport of food; and
(ii) to a manufacturer or other person that--
(I) arranges for the transportation of food by a carrier; or
(II) furnishes a tank vehicle or bulk vehicle for the transportation of food; and
(E) recordkeeping; and
(2) include--
(A) a list of nonfood products that the Secretary determines may, if shipped in a bulk vehicle,
render adulterated food that is subsequently transported in the same vehicle; and
(B) a list of nonfood products that the Secretary determines may, if shipped in a motor vehicle
or rail vehicle (other than a tank vehicle or bulk vehicle), render adulterated food that is
simultaneously or subsequently transported in the same vehicle.
(d) Waivers.
(1) In general. The Secretary may waive any requirement under this section, with respect to
any class of persons, vehicles, food, or nonfood products, if the Secretary determines that the
waiver--
(A) will not result in the transportation of food under conditions that would be unsafe for human
or animal health; and
(B) will not be contrary to the public interest.
(2) Publication. The Secretary shall publish in the Federal Register any waiver and the
reasons for the waiver.
(e) Preemption.
(1) In general. A requirement of a State or political subdivision of a State that concerns the
transportation of food is preempted if--
(A) complying with a requirement of the State or political subdivision and a requirement of this
section, or a regulation prescribed under this section, is not possible; or
(B) the requirement of the State or political subdivision as applied or enforced is an obstacle to
accomplishing and carrying out this section or a regulation prescribed under this section.
(2) Applicability. This subsection applies to transportation that occurs on or after the effective
date of the regulations promulgated under subsection (b).
(f) Assistance of other agencies. The Secretary of Transportation, the Secretary of Agriculture,
the Administrator of the Environmental Protection Agency, and the heads of other Federal
agencies, as appropriate, shall provide assistance on request, to the extent resources are
available, to the Secretary for the purposes of carrying out this section.
Footnotes: Chapter IV
1. See footnote for section 403(h)(3) regarding the stylistic use of a list consisting of "(a)",
"(b)", etc.
2. So in law. See section 3(i)(1) of Public Law 103–80. Probably should be "or".
3. Subparagraph (2) appears so as to reflect the probable intent of the Congress. Section 404
of Public Law 104–170 (110 Stat. 1514) had amendatory instructions whose probable intended
effect was to strike the existing subparagraph (2) and to insert a substitute subparagraph (2).
These included instructions to strike "(2)(A) if it bears'" and all that follows through "(3) if it
consists", but "(3) If it consists" was the language that actually appeared. (Previously, section
3(i) of Public Law 103–80 (107 Stat. 776) had amended subparagraph (3) by striking "if it" and
inserting "If it".)
4. So in law. Probably should be "subparagraph".
5. See footnote for paragraph (h)(3) regarding the stylistic use of a list consisting of "(a)",
"(b)", etc.
6. References are so in law. See section 10808(b)(3) of Public Law 107–171 (116 Stat. 530).
In order to be consistent with other cross-references within section 403 above, each reference
in section 403(h)(3) to a paragraph, subparagraph, clause, or subclause should be a reference
to a subparagraph, clause, subclause, or item, respectively. See, for example,
cross-references in paragraph (q) (relating to nutrition information) and paragraph (r) (relating
to nutrient levels and health claims).
Section 403 was enacted in 1938 and has organizational units and cross-references that are
not in accordance with modern practice. In modern practice, "(a)" is a subsection, "(1)" is a
paragraph, "(A)" is a subparagraph, "(i)" is a clause, "(I)" is a subclause, "(aa)" is an item, and
"(AA)" is a subitem. The references in section 403(h)(3) follow this practice.
In modern practice, all of the section 403 text would be considered an undesignated
subsection, and the list that begins after "A food shall be deemed to be misbranded—" would
consist of paragraphs (1), (2), etc.
In section 403, however, the original authors of the 1938 Act used a list consisting of (a), (b),
etc., and the authors referred to "(a)" as a paragraph, "(1)" as a subparagraph, "(A)" as a
clause, and "(i)" as a subclause. (Express references to organizational units below the "(i)"
level have been avoided.)
The original authors followed this approach in each section in this Act whose text was a list
consisting of (a), (b), etc. Such sections include sections 201, 301, 402, 403, 501, 502, 601,
and 602.
Some of these sections have numerous internal cross-references. Rather than conforming
each of these to the modern practice, the usual approach in making amendments to these
sections has been to follow the approach used by the original authors of the 1938 Act.
7. So in law. Probably should be followed by a comma.
8. Paragraph (o) was repealed by Public Law 106–554 (114 Stat. 2763A–73). Paragraph (p)
was struck by Public Law 104–124 (110 Stat. 882).
9. Public Law 101–535, which was enacted November 8, 1990.
10. 1 Section 403(t) was added by subsection (a)(2) of section 10806 of Public Law 107–171
(116 Stat. 526). Subsection (a)(1) of such section 10806 provides as follows:
(1) IN GENERAL.—Notwithstanding any other provision of law, for purposes of the Federal
Food, Drug, and Cosmetic Act (21 U.S.C. 301 et seq.)—
(A) the term "catfish" may only be considered to be a common or usual name (or part thereof)
for fish classified within the family Ictaluridae; and
(B) only labeling or advertising for fish classified within that family may include the term
"catfish"
11. Section 403(u) was added by subsection (b)(2) of section 10806 of Public Law 107–171
(116 Stat. 527). Subsection (b)(1) of such section 10806 provides as follows:
(1) IN GENERAL.—Notwithstanding any other provision of law, for purposes of the Federal
Food, Drug, and Cosmetic Act (21 U.S.C. 301 et seq.)—
(A) the term "ginseng" may only be considered to be a common or usual name (or part thereof)
for any herb or herbal ingredient derived from a plant classified within the genus Panax; and
(B) only labeling or advertising for herbs or herbal ingredients classified within that
genus may include the term ‘‘ginseng’’.
12. Paragraphs (w) and (x) were added by section 203(a) of Public Law 108–282. Section
203(d) provides as follows:
(d) EFFECTIVE DATE.—The amendments made by this section shall apply to any food that is
labeled on or after January 1, 2006.
13. Section 203(b) of Public Law 108–282 provides as follows:
(b) EFFECT ON OTHER AUTHORITY.—The amendments made by this section that require a
label or labeling for major food allergens do not alter the authority of the Secretary of Health
and Human Services under the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301 et seq.)
to require a label or labeling for other food allergens.
14. Several provisions of paragraph (w) contain cross-references to other provisions of the
paragraph, and also references to other provisions of this section (section 403). The
references to subsections, paragraphs, and subparagraphs probably should be references to
paragraphs, subparagraphs, and clauses, respectively. See footnote for paragraph (h)(3).
15. Public Law 108–282 contains several sections concerning food allergens that do not make
amendments to this Act (the Federal Food, Drug, and Cosmetic Act). Section 204 concerns a
report to congressional committees; section 205 concerns inspections; section 206 concerns
gluten labeling; section 207 concerns improvements in the collection and publication of data;
section 208 concerns research; section 209 concerns the Food Code; and section 210
concerns recommendations regarding responding to food-related allergic responses.
16. See footnote 1 to paragraph (w) regarding an effective date, and see footnote 2 to such
paragraph regarding the authority of the Secretary of Health and Human Services.
17. So in law. Probably should be "paragraph (g), (i), or (k)". See footnote 3 for paragraph (w).
18. Section 403A was enacted without a section heading. See section 6(a) of Public Law 101–
535 (104 Stat. 2362).
19. See the revolving fund provision in the appendix.
20. Section 4 of Public Law 81–459 (64 Stat. 20) amended section 15 of the Federal Trade
Commission Act (15 U.S.C. 55) by adding the following subsection:
"(f) For the purposes of this section and section 407 of the Federal Food, Drug, and Cosmetic
Act, as amended, the term 'oleomargarine' or 'margarine' includes—
"(1) all substances, mixtures, and compounds known as oleomargarine or margarine;
"(2) all substances, mixtures, and compounds which have a consistence similar to that of
butter and which contain any edible oils or fats other than milk fat if made in imitation
or semblance of butter."
In repealing section 2301 of the Internal Revenue Code (relating to the tax on oleomargarine)
Public Law 81–459 declared, in part: "The Congress hereby finds and declares that the sale,
or the serving in public eating places, of colored oleomargarine or colored margarine without
clear identification as such or which is otherwise adulterated or misbranded within the meaning
of the Federal Food, Drug, and Cosmetic Act depresses the market in interstate commerce for
butter and for oleomargarine or margarine clearly identified and neither adulterated nor
misbranded, and constitutes a burden on interstate commerce in such articles. Such burden
exists, irrespective of whether such oleomargarine or margarine originates from an interstate
source or from the State in which it is sold."
Section 6 of such Public Law states that "nothing in this Act shall be construed as authorizing
the possession, sale, or serving of colored oleomargarine or colored margarine in any State or
Territory in contravention of the laws of such State or Territory."
21. So in law. Probably should be "(except paragraphs (a) and (f))".
22. See footnote for section 406.
23. Section 501(d)(2) of division G of Public Law 108–199 (118 Stat. 422) provides as follows:
(2) TOLERANCE FEES.—Notwithstanding section 408(m)(1) of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. 346a(m)(1)), during the period beginning on October 1, 2003, and
ending on September 30, 2008, the Administrator of the Environmental Protection Agency
shall not collect any tolerance fees under that section.
24. Indentation is so in law. Beginning of sentence probably should be moved to left.
25. So in law. The word "Authorization" probably should appear after "Demonstration".
26. So in law. Probably should be "subsection".
27. So in law. Probably should be "paragraph".
CHAPTER V—DRUGS AND DEVICES SUBCHAPTER A—DRUGS AND DEVICES
ADULTERATED DRUGS AND DEVICES
SEC. 501. [21 U.S.C. 351] A drug or device shall be deemed to be adulterated— 1
(a)(1) If it consists in whole or in part of any filthy, putrid, or decomposed substance; or (2)(A) if
it has been prepared, packed, or held under insanitary conditions whereby it may have been
contaminated with filth, or whereby it may have been rendered injurious to health; or (B) if it is
a drug and the methods used in, or the facilities or controls used for, its manufacture,
processing, packing, or holding do not conform to or are not operated or administered in
conformity with current good manufacturing practice to assure that such drug meets the
requirements of this Act as to safety and has the identity and strength, and meets the quality
and purity characteristics, which it purports or is represented to possess; or (C) if it is a
compounded positron emission tomography drug and the methods used in, or the facilities and
controls used for, its compounding, processing, packing, or holding do not conform to or are
not operated or administered in conformity with the positron emission tomography
compounding standards and the official monographs of the United States Pharmacopoeia to
assure that such drug meets the requirements of this Act as to safety and has the identity and
strength, and meets the quality and purity characteristics, that it purports or is represented to
possess; or (3) if its container is composed, in whole or in part, of any poisonous or deleterious
substance which may render the contents injurious to health; or (4) if (A) it bears or contains,
for purposes of coloring only, a color additive which is unsafe within the meaning of section
721(a), or (B) it is a color additive the intended use of which in or on drugs or devices is for
purposes of coloring only and is unsafe within the meaning of section 721(a); or (5) if it is a
new animal drug which is unsafe within the meaning of section 512; or (6) if it is an animal feed
bearing or containing a new animal drug, and such animal feed is unsafe within the meaning of
section 512.
(b) If it purports to be or is represented as a drug the name of which is recognized in an official
compendium, and its strength differs from, or its quality or purity falls below, the standards set
forth in such compendium. Such determination as to strength, quality, or purity shall be made
in accordance with the tests or methods of assay set forth in such compendium, except that
whenever tests or methods of assay have not been prescribed in such compendium, or such
tests or methods of assay as are prescribed are, in the judgment of the Secretary, insufficient
for the making of such determination, the Secretary shall bring such fact to the attention of the
appropriate body charged with the revision of such compendium, and if such body fails within a
reasonable time to prescribe tests or methods of assay which, in the judgment of the Secretary,
are sufficient for purposes of this paragraph, then the Secretary shall promulgate regulations
prescribing appropriate tests or methods of assay in accordance with which such
determination as to strength, quality, or purity shall be made. No drug defined in an official
compendium shall be deemed to be adulterated under this paragraph because it differs from
the standard of strength, quality, or purity therefor set forth in such compendium, if its
difference in strength, quality, or purity from such standards is plainly stated on its label.
Whenever a drug is recognized in both the United States Pharmacopeia and the Homeopathic
Pharmacopeia of the United States it shall be subject to the requirements of the United States
Pharmacopeia unless it is labeled and offered for sale as a homeopathic drug, in which case it
shall be subject to the provisions of the Homeopathic Pharmacopeia of the United States and
not to those of the United States Pharmacopeia.
(c) If it is not subject to the provisions of paragraph (b) of this section and its strength differs
from, or its purity or quality falls below, that which it purports or is represented to possess.
(d) If it is a drug and any substance has been (1) mixed or packed therewith so as to reduce its
quality or strength or (2) substituted wholly or in part therefor.
(e)(1) If it is, or purports to be or is represented as, a device which is subject to a performance
standard established under section 514, unless such device is in all respects in conformity with
such standard.
(2) If it is declared to be, purports to be, or is represented as, a device that is in conformity with
any standard recognized under section 514(c) unless such device is in all respects in
conformity with such standard.
(f)(1) If it is a class III device—
(A)(i) which is required by a regulation promulgated under subsection (b) of section 515 to
have an approval under such section of an application for premarket approval and which is not
exempt from section 515 under section 520(g), and
(ii)(I) for which an application for premarket approval or a notice of completion of a product
development protocol was not filed with the Secretary within the ninety-day period beginning
on the date of the promulgation of such regulation, or
(II) for which such an application was filed and approval of the application has been denied,
suspended, or withdrawn, or such a notice was filed and has been declared not completed or
the approval of the device under the protocol has been withdrawn;
(B)(i) which was classified under section 513(f) into class III, which under section 515(a) is
required to have in effect an approved application for premarket approval, and which is not
exempt from section 515 under section 520(g), and
(ii) which has an application which has been suspended or is otherwise not in effect; or
(C) which was classified under section 520(l) into class III, which under such section is
required to have in effect an approved application under section 515, and which has an
application which has been suspended or is otherwise not in effect.
(2)(A) In the case of a device classified under section 513(f) into class III and intended solely
for investigational use, paragraph (1)(B) shall not apply with respect to such device during the
period ending on the ninetieth day after the date of the promulgation of the regulations
prescribing the procedures and conditions required by section 520(g)(2).
(B) In the case of a device subject to a regulation promulgated under subsection (b) of section
515, paragraph 2 (1) shall not apply with respect to such device during the period ending—
(i) on the last day of the thirtieth calendar month beginning after the month in which the
classification of the device in class III became effective under section 513, or
(ii) on the ninetieth day after the date of the promulgation of such regulation, whichever occurs
later.
(g) If it is a banned device.
(h) If it is a device and the methods used in, or the facilities or controls used for, its
manufacture, packing, storage, or installation are not in conformity with applicable
requirements under section 520(f)(1) or an applicable condition prescribed by an order under
section 520(f)(2).
(i) If it is a device for which an exemption has been granted under section 520(g) for
investigational use and the person who was granted such exemption or any investigator who
uses such device under such exemption fails to comply with a requirement prescribed by or
under such section.
MISBRANDED DRUGS AND DEVICES
SEC. 502. [21 U.S.C. 352] A drug or device shall be deemed to be misbranded 3
(a) False or misleading label. If its labeling is false or misleading in any particular. Health care
economic information provided to a formulary committee, or other similar entity, in the course
of the committee or the entity carrying out its responsibilities for the selection of drugs for
managed care or other similar organizations, shall not be considered to be false or misleading
under this paragraph if the health care economic information directly relates to an indication
approved under section 505 or under section 351(a) of the Public Health Service Act [42
USCS § 262(a)] for such drug and is based on competent and reliable scientific evidence. The
requirements set forth in section 505(a) or in section 351(a) of the Public Health Service Act
shall not apply to health care economic information provided to such a committee or entity in
accordance with this paragraph. Information that is relevant to the substantiation of the health
care economic information presented pursuant to this paragraph shall be made available to
the Secretary upon request. In this paragraph, the term "health care economic information"
means any analysis that identifies, measures, or compares the economic consequences,
including the costs of the represented health outcomes, of the use of a drug to the use of
another drug, to another health care intervention, or to no intervention.
(b) Package form; contents of label. If in package form unless it bears a label containing (1) the
name and place of business of the manufacturer, packer, or distributor; and (2) an accurate
statement of the quantity of the contents in terms of weight, measure, or numerical count:
Provided, That under clause (2) of this paragraph reasonable variations shall be permitted,
and exemptions as to small packages shall be established, by regulations prescribed by the
Secretary.
(c) Prominence of information on label. If any word, statement, or other information required by
or under authority of this Act to appear on the label or labeling is not prominently placed
thereon with such conspicuousness (as compared with other words, statements, designs, or
devices, in the labeling) and in such terms as to render it likely to be read and understood by
the ordinary individual under customary conditions of purchase and use.
(d) [Repealed] 4
(e) Designation of drugs or devices by established names.
(1)(A) If it is a drug, unless its label bears, to the exclusion of any other nonproprietary name
(except the applicable systematic chemical name or the chemical formula)
(i) the established name (as defined in subparagraph (3)) of the drug, if there is such a name;
(ii) the established name and quantity or, if determined to be appropriate by the Secretary, the
proportion of each active ingredient, including the quantity, kind, and proportion of any alcohol,
and also including whether active or not the established name and quantity or if determined to
be appropriate by the Secretary, the proportion of any bromides, ether, chloroform, acetanilide,
acetophenetidin, amidopyrine, antipyrine, atropine, hyoscine, hyoscyamine, arsenic, digitalis,
digitalis glucosides, mercury, ouabain, strophanthin, strychnine, thyroid, or any derivative or
preparation of any such substances, contained therein, except that the requirement for stating
the quantity of the active ingredients, other than the quantity of those specifically named in this
subclause, shall not apply to nonprescription drugs not intended for human use; and
(iii) the established name of each inactive ingredient listed in alphabetical order on the outside
container of the retail package and, if determined to be appropriate by the Secretary, on the
immediate container, as prescribed in regulation promulgated by the Secretary, except that
nothing in this subclause shall be deemed to require that any trade secret be divulged, and
except that the requirements of this subclause with respect to alphabetical order shall apply
only to nonprescription drugs that are not also cosmetics and that this subclause shall not
apply to nonprescription drugs not intended for human use.
(B) For any prescription drug the established name of such drug or ingredient, as the case may
be, on such label (and on any labeling on which a name for such drug or ingredient is used)
shall be printed prominently and in type at least half as large as that used thereon for any
proprietary name or designation for such drug or ingredient, except that to the extent that
compliance with the requirements of subclause (ii) or (iii) of clause (A) or this clause is
impracticable, exemptions shall be established by regulations promulgated by the Secretary.
(2) If it is a device and it has an established name, unless its label bears, to the exclusion of
any other nonproprietary name, its established name (as defined in subparagraph (4))
prominently printed in type at least half as large as that used thereon for any proprietary name
or designation for such device, except that to the extent compliance with the requirements of
this subparagraph is impracticable, exemptions shall be established by regulations
promulgated by the Secretary.
(3) As used in subparagraph (1), the term "established name", with respect to a drug or
ingredient thereof, means (A) the applicable official name designated pursuant to section 508,
or (B) if there is no such name and such drug, or such ingredient, is an article recognized in an
official compendium, then the official title thereof in such compendium, or (C) if neither clause
(A) nor clause (B) of this subparagraph applies, then the common or usual name, if any, of
such drug or of such ingredient, except that where clause (B) of this subparagraph applies to
an article recognized in the United States Pharmacopeia and in the Homoeopathic
Pharmacopoeia under different official titles, the official title used in the United States
Pharmacopeia shall apply unless it is labeled and offered for sale as a homoeopathic drug, in
which case the official title used in the Homoeopathic Pharmacopoeia shall apply.
(4) As used in subparagraph (2), the term "established name" with respect to a device means
(A) the applicable official name of the device designated pursuant to section 508, (B) if there is
no such name and such device is an article recognized in an official compendium, then the
official title thereof in such compendium, or (C) if neither clause (A) nor clause (B) of this
subparagraph applies, then any common or usual name of such device.
(f) Directions for use and warnings on label. Unless its labeling bears (1) adequate directions
for use; and (2) such adequate warnings against use in those pathological conditions or by
children where its use may be dangerous to health, or against unsafe dosage or methods or
duration of administration or application, in such manner and form, as are necessary for the
protection of users, except that where any requirement of clause (1) of this paragraph, as
applied to any drug or device, is not necessary for the protection of the public health, the
Secretary shall promulgate regulations exempting such drug or device from such requirement.
Required labeling for prescription devices intended for use in health care facilities or by a
health care professional and required labeling for in vitro diagnostic devices intended for use
by health care professionals or in blood establishments may be made available solely by
electronic means, provided that the labeling complies with all applicable requirements of law,
and that the manufacturer affords such users the opportunity to request the labeling in paper
form, and after such request, promptly provides the requested information without additional
cost.
(g) Representations as recognized drug; packing and labeling; inconsistent requirements for
designation of drug. If it purports to be a drug the name of which is recognized in an official
compendium, unless it is packaged and labeled as prescribed therein. The method of packing
may be modified with the consent of the Secretary. Whenever a drug is recognized in both the
United States Pharmacopoeia and the Homoeopathic Pharmacopoeia of the United States, it
shall be subject to the requirements of the United States Pharmacopoeia with respect to
packaging and labeling unless it is labeled and offered for sale as a homoeopathic drug, in
which case it shall be subject to the provisions of the Homoeopathic Pharmacopoeia of the
United States, and not to those of the United States Pharmacopeia, except that in the event of
inconsistency between the requirements of this paragraph and those of paragraph (e) as to the
name by which the drug or its ingredients shall be designated, the requirements of paragraph
(e) shall prevail.
(h) Deteriorative drugs; packing and labeling. If it has been found by the Secretary to be a drug
liable to deterioration, unless it is packaged in such form and manner, and its label bears a
statement of such precautions, as the Secretary shall by regulations require as necessary for
the protection of the public health. No such regulation shall be established for any drug
recognized in an official compendium until the Secretary shall have informed the appropriate
body charged with the revision of such compendium of the need for such packaging or labeling
requirements and such body shall have failed within a reasonable time to prescribe such
requirements.
(i) Drug; misleading container; imitation; offer for sale under another name. (1) If it is a drug
and its container is so made, formed, or filled as to be misleading; or (2) if it is an imitation of
another drug; or (3) if it is offered for sale under the name of another drug.
(j) Health-endangering when used as prescribed. If it is dangerous to health when used in the
dosage or manner; or with the frequency or duration prescribed, recommended, or suggested
in the labeling thereof.
(k), (l) [Repealed] 5
(m) Color additives; packing and labeling. If it is a color additive the intended use of which is for
the purpose of coloring only, unless its packaging and labeling are in conformity with such
packaging and labeling requirements applicable to such color additive, as may be contained in
regulations issued under section 721.
(n) Prescription drug advertisements: established name; quantitative formula; side effects,
contraindications, and effectiveness; prior approval; false advertising; labeling; construction of
the Convention on Psychotropic Substances. In the case of any prescription drug distributed or
offered for sale in any State, unless the manufacturer, packer, or distributor thereof includes in
all advertisements and other descriptive printed matter issued or caused to be issued by the
manufacturer, packer, or distributor with respect to that drug a true statement of (1) the
established name as defined in section 502(e) 6 [subsec. (e) of this section], printed
prominently and in type at least half as large as that used for any trade or brand name thereof,
(2) the formula showing quantitatively each ingredient of such drug to the extent required for
labels under section 502(e) [subsec. (e) of this section] 6, and (3) such other information in
brief summary relating to side effects, contraindications, and effectiveness as shall be required
in regulations which shall be issued by the Secretary in accordance with the procedure
specified in section 701(e) of this Act, except that (A) except in extraordinary circumstances,
no regulation issued under this paragraph shall require prior approval by the Secretary of the
content of any advertisement, and (B) no advertisement of a prescription drug, published after
the effective date of regulations issued under this paragraph applicable to advertisements of
prescription drugs, shall, with respect to the matters specified in this paragraph or covered by
such regulations, be subject to the provisions of sections 12 through 17 of the Federal Trade
Commission Act, as amended [15 USC 52–57]. This paragraph (n) 7 shall not be applicable to
any printed matter which the Secretary determines to be labeling as defined in section 201(m)
of this Act. Nothing in the Convention on Psychotropic Substances, signed at Vienna, Austria,
on February 21, 1971, shall be construed to prevent drug price communications to consumers.
8
(o) Drugs or devices from nonregistered establishments. If it was manufactured, prepared,
propagated, compounded, or processed in an establishment in any State not duly registered
under section 510, if it was not included in a list required by section 510(j), if a notice or other
information respecting it was not provided as required by such section or section 510(k), or if it
does not bear such symbols from the uniform system for identification of devices prescribed
under section 510(e) as the Secretary by regulation requires.
(p) Packaging or labeling of drugs in violation of regulations. If it is a drug and its packaging or
labeling is in violation of an applicable regulation issued pursuant to section 3 or 4 of the
Poison Prevention Packaging Act of 1970 [15 USCS § 1472 or 1473].
(q) Restricted devices using false or misleading advertising or used in violation of regulations.
In the case of any restricted device distributed or offered for sale in any State, if (1) its
advertising is false or misleading in any particular, or (2) it is sold, distributed, or used in
violation of regulations prescribed under section 520(e).
(r) Restricted devices not carrying requisite accompanying statements in advertisements and
other descriptive printed matter. In the case of any restricted device distributed or offered for
sale in any State, unless the manufacturer, packer, or distributor thereof includes in all
advertisements and other descriptive printed matter issued or caused to be issued by the
manufacturer, packer, or distributor with respect to that device (1) a true statement of the
device’s established name as defined in section 502(e), printed prominently and in type at
least half as large as that used for any trade or brand name thereof, and (2) a brief statement
of the intended uses of the device and relevant warnings, precautions, side effects, and
contraindications and, in the case of specific devices made subject to a finding by the
Secretary after notice and opportunity for comment that such action is necessary to protect the
public health, a full description of the components of such device or the formula showing
quantitatively each ingredient of such device to the extent required in regulations which shall
be issued by the Secretary after an opportunity for a hearing. Except in extraordinary
circumstances, no regulation issued under this paragraph shall require prior approval by the
Secretary of the content of any advertisement and no advertisement of a restricted device,
published after the effective date of this paragraph shall, with respect to the matters specified
in this paragraph or covered by regulations issued hereunder, be subject to the provisions of
sections 12 through 15 of the Federal Trade Commission Act [15 U.S.C. 52–55]. This
paragraph shall not be applicable to any printed matter which the Secretary determines to be
labeling as defined in section 201(m).
(s) Devices subject to performance standards not bearing requisite labeling. If it is a device
subject to a performance standard established under section 514, unless it bears such labeling
as may be prescribed in such performance standard.
(t) Devices for which there has been a failure or refusal to give required notification or to
furnish required material or information. If it is a device and there was a failure or refusal (1) to
comply with any requirement prescribed under section 518 respecting the device, (2) to furnish
any material or information required by or under section 519 respecting the device, or (3) to
comply with a requirement under section 522.
9 (u) Identification of manufacturer.
(1) Subject to paragraph (2), if it is a reprocessed single-use device, unless it, or an
attachment thereto, prominently and conspicuously bears the name of the manufacturer of the
reprocessed device, a generally recognized abbreviation of such name, or a unique and
generally recognized symbol identifying such manufacturer.
(2) If the original device or an attachment thereto does not prominently and conspicuously bear
the name of the manufacturer of the original device, a generally recognized abbreviation of
such name, or a unique and generally recognized symbol identifying such manufacturer, a
reprocessed device may satisfy the requirements of paragraph (1) through the use of a
detachable label on the packaging that identifies the manufacturer and is intended to be
affixed to the medical record of a patient.
10 (v) Reprocessed single-use device. If it is a reprocessed single-use device, unless all
labeling of the device prominently and conspicuously bears the statement "Reprocessed
device for single use. Reprocessed by ------." The name of the manufacturer of the
reprocessed device shall be placed in the space identifying the person responsible for
reprocessing.
(w) New animal drugs. If it is a new animal drug—
(1) that is conditionally approved under section 571 and its labeling does not conform with the
approved application or section 571(f), or that is not conditionally approved under section 571
and its label bears the statement set forth in section 571(f)(1)(A); or
(2) that is indexed under section 572 and its labeling does not conform with the index listing
under section 572(e) or 572(h), or that has not been indexed under section 572 and its label
bears the statement set forth in section 572(h).
(x) [Caution: This subsection is effective and applicable to any nonprescription drug
labeled on or after the date that is 1 year after enactment, pursuant to § 2(e)(1), (2) of Act
Dec. 22, 2006, P.L. 109-462, which appears as a note to this section.]. If it is a
nonprescription drug (as defined in section 760) that is marketed in the United States, unless
the label of such drug includes a domestic address or domestic phone number through which
the responsible person (as described in section 760) may receive a report of a serious adverse
event (as defined in section 760) with such drug.
EXEMPTIONS AND CONSIDERATION FOR CERTAIN DRUGS, DEVICES, AND
BIOLOGICAL PRODUCTS
SEC. 503. (21 U.S.C. 353) (a) The Secretary is hereby directed to promulgate regulations
exempting from any labeling or packaging requirement of this Act drugs and devices which are,
in accordance with the practice of the trade, to be processed, labeled, or repacked in
substantial quantities at establishments other than those where originally processed or packed,
on condition that such drugs and devices are not adulterated or misbranded, under the
provisions of this Act upon removal from such processing, labeling, or repacking
establishment.
(b)(1) A drug intended for use by man which—
(A) because of its toxicity or other potentiality for harmful effect, or the method of its use, or the
collateral measures necessary to its use, is not safe for use except under the supervision of a
practitioner licensed by law to administer such drug; or
(B) is limited by an approved application under section 505 to use under the professional
supervision of a practitioner licensed by law to administer such drug; shall be dispensed only (i)
upon a written prescription of a practitioner licensed by law to administer such drug, or (ii) upon
an oral prescription of such practitioner which is reduced promptly to writing and filed by the
pharmacist, or (iii) by refilling any such written or oral prescription if such refilling is authorized
by the prescriber either in the original prescription or by oral order which is reduced promptly to
writing and filed by the pharmacist. The act of dispensing a drug contrary to the provisions of
this paragraph shall be deemed to be an act which results in the drug being misbranded while
held for sale.
(2) Any drug dispensed by filling or refilling a written or oral prescription of a practitioner
licensed by law to administer such drug shall be exempt from the requirements of section 502,
except paragraphs (a), (i) (2) and (3), (k), and (l), and the packaging requirements of
paragraphs (g), (h), and (p), if the drug bears a label containing the name and address of the
dispenser, the serial number and date of the prescription or of its filling, the name of the
prescriber, and, if stated in the prescription, the name of the patient, and the directions for use
and cautionary statements, if any, contained in such prescription. This exemption shall not
apply to any drug dispensed in the course of the conduct of a business of dispensing drugs
pursuant to diagnosis by mail, or to a drug dispensed in violation of paragraph (1) of this
subsection.
(3) The Secretary may by regulation remove drugs subject to section 505 from the
requirements of paragraph (1) of this subsection when such requirements are not necessary
for the protection of the public health.
(4)(A) A drug that is subject to paragraph (1) shall be deemed to be misbranded if at any time
prior to dispensing the label of the drug fails to bear, at a minimum, the symbol ‘‘Rx only’’.
(B) A drug to which paragraph (1) does not apply shall be deemed to be misbranded if at any
time prior to dispensing the label of the drug bears the symbol described in subparagraph (A).
(5) Nothing in this subsection shall be construed to relieve any person from any requirement
prescribed by or under authority of law with respect to drugs now included or which may
hereafter be included within the classifications stated in section 3220 of the Internal Revenue
Code (26 U.S.C. 3220), or to marihuana as defined in section 3238(b) of the Internal Revenue
Code (26 U.S.C. 3238(b)).
(c)(1) No person may sell, purchase, or trade or offer to sell, purchase, or trade any drug
sample. For purposes of this paragraph and subsection (d), the term ‘‘drug sample’’ means a
unit of a drug, subject to subsection (b), which is not intended to be sold and is intended to
promote the sale of the drug. Nothing in this paragraph shall subject an officer or executive of
a drug manufacturer or distributor to criminal liability solely because of a sale, purchase, trade,
or offer to sell, purchase, or trade in violation of this paragraph by other employees of the
manufacturer or distributor.
(2) No person may sell, purchase, or trade, offer to sell, purchase, or trade, or counterfeit any
coupon. For purposes of this paragraph, the term ‘‘coupon’’ means a form which may be
redeemed, at no cost or at a reduced cost, for a drug which is prescribed in accordance with
subsection (b).
(3)(A) No person may sell, purchase, or trade, or offer to sell, purchase, or trade, any drug—
(i) which is subject to subsection (b), and
(ii)(I) which was purchased by a public or private hospital or other health care entity, or
(II) which was donated or supplied at a reduced price to a charitable organization described in
section 501(c)(3) of the Internal Revenue Code of 1954.
(B) Subparagraph (A) does not apply to—
(i) the purchase or other acquisition by a hospital or other health care entity which is a member
of a group purchasing organization of a drug for its own use from the group purchasing
organization or from other hospitals or health care entities which are members of such
organization,
(ii) the sale, purchase, or trade of a drug or an offer to sell, purchase, or trade a drug by an
organization described in subparagraph (A)(ii)(II) to a nonprofit affiliate of the organization to
the extent otherwise permitted by law,
(iii) a sale, purchase, or trade of a drug or an offer to sell, purchase, or trade a drug among
hospitals or other health care entities which are under common control,
(iv) a sale, purchase, or trade of a drug or an offer to sell, purchase, or trade a drug for
emergency medical reasons, or
(v) a sale, purchase, or trade of a drug, an offer to sell, purchase, or trade a drug, or the
dispensing of a drug pursuant to a prescription executed in accordance with subsection (b).
For purposes of this paragraph, the term ‘‘entity’’ does not include a wholesale distributor of
drugs or a retail pharmacy licensed under State law and the term ‘‘emergency medical
reasons’’ includes transfers of a drug between health care entities or from a health care entity
to a retail pharmacy undertaken to alleviate temporary shortages of the drug arising from
delays in or interruptions of regular distribution schedules.
(d)(1) Except as provided in paragraphs (2) and (3), no person may distribute any drug sample.
For purposes of this subsection, the term ‘‘distribute’’ does not include the providing of a drug
sample to a patient by a—
(A) practitioner licensed to prescribe such drug,
(B) health care professional acting at the direction and under the supervision of such a
practitioner, or
(C) pharmacy of a hospital or of another health care entity that is acting at the direction of such
a practitioner and that received such sample pursuant to paragraph (2) or (3).
(2)(A) The manufacturer or authorized distributor of record of a drug subject to subsection (b)
may, in accordance with this paragraph, distribute drug samples by mail or common carrier to
practitioners licensed to prescribe such drugs or, at the request of a licensed practitioner, to
pharmacies of hospitals or other health care entities. Such a distribution of drug samples may
only be made—
(i) in response to a written request for drug samples made on a form which meets the
requirements of subparagraph (B), and
(ii) under a system which requires the recipient of the drug sample to execute a written receipt
for the drug sample upon its delivery and the return of the receipt to the manufacturer or
authorized distributor of record.
(B) A written request for a drug sample required by subparagraph (A)(i) shall contain—
(i) the name, address, professional designation, and signature of the practitioner making the
request,
(ii) the identity of the drug sample requested and the quantity requested,
(iii) the name of the manufacturer of the drug sample requested, and
(iv) the date of the request.
(C) Each drug manufacturer or authorized distributor of record which makes distributions by
mail or common carrier under this paragraph shall maintain, for a period of 3 years, the request
forms submitted for such distributions and the receipts submitted for such distributions and
shall maintain a record of distributions of drug samples which identifies the drugs distributed
and the recipients of the distributions. Forms, receipts, and records required to be maintained
under this subparagraph shall be made available by the drug manufacturer or authorized
distributor of record to Federal and State officials engaged in the regulation of drugs and in the
enforcement of laws applicable to drugs.
(3) The manufacturer or authorized distributor of record of a drug subject to subsection (b) may,
by means other than mail or common carrier, distribute drug samples only if the manufacturer
or authorized distributor of record makes the distributions in accordance with subparagraph (A)
and carries out the activities described in subparagraphs (B) through (F) as follows:
(A) Drug samples may only be distributed—
(i) to practitioners licensed to prescribe such drugs if they make a written request for the drug
samples, or
(ii) at the written request of such a licensed practitioner, to pharmacies of hospitals or other
health care entities. A written request for drug samples shall be made on a form which
contains the practitioner’s name, address, and professional designation, the identity of the
drug sample requested, the quantity of drug samples requested, the name of the manufacturer
or authorized distributor of record of the drug sample, the date of the request and signature of
the practitioner making the request.
(B) Drug manufacturers or authorized distributors of record shall store drug samples under
conditions that will maintain their stability, integrity, and effectiveness and will assure that the
drug samples will be free of contamination, deterioration, and adulteration.
(C) Drug manufacturers or authorized distributors of record shall conduct, at least annually, a
complete and accurate inventory of all drug samples in the possession of representatives of
the manufacturer or authorized distributor of record. Drug manufacturers or authorized
distributors of record shall maintain lists of the names and address of each of their
representatives who distribute drug samples and of the sites where drug samples are stored.
Drug manufacturers or authorized distributors of record shall maintain records for at least 3
years of all drug samples distributed, destroyed, or returned to the manufacturer or authorized
distributor of record, of all inventories maintained under this subparagraph, of all thefts or
significant losses of drug samples, and of all requests made under subparagraph (A) for drug
samples. Records and lists maintained under this subparagraph shall be made available by
the drug manufacturer or authorized distributor of record to the Secretary upon request.
(D) Drug manufacturers or authorized distributors of record shall notify the Secretary of any
significant loss of drug samples and any known theft of drug samples.
(E) Drug manufacturers or authorized distributors of record shall report to the Secretary any
conviction of their representatives for violations of subsection (c)(1) or a State law because of
the sale, purchase, or trade of a drug sample or the offer to sell, purchase, or trade a drug
sample.
(F) Drug manufacturers or authorized distributors of record shall provide to the Secretary the
name and telephone number of the individual responsible for responding to a request for
information respecting drug samples.
(e)(1)(A) Each person who is engaged in the wholesale distribution of a drug subject to
subsection (b) and who is not the manufacturer or an authorized distributor of record of such
drug shall, before each wholesale distribution of such drug (including each distribution to an
authorized distributor of record or to a retail pharmacy), provide to the person who receives the
drug a statement (in such form and containing such information as the Secretary may require)
identifying each prior sale, purchase, or trade of such drug (including the date of the
transaction and the names and addresses of all parties to the transaction).
(B) Each manufacturer of a drug subject to subsection (b) shall maintain at its corporate offices
a current list of the authorized distributors of record of such drug.
(2)(A) No person may engage in the wholesale distribution in interstate commerce of drugs
subject to subsection (b) in a State unless such person is licensed by the State in accordance
with the guidelines issued under subparagraph (B).
(B) The Secretary shall by regulation issue guidelines establishing minimum standards, terms,
and conditions for the licensing of persons to make wholesale distributions in interstate
commerce of drugs subject to subsection (b). Such guidelines shall prescribe requirements for
the storage and handling of such drugs and for the establishment and maintenance of records
of the distributions of such drugs.
(3) For the purposes of this subsection and subsection (d)—
(A) the term ‘‘authorized distributors of record’’ means those distributors with whom a
manufacturer has established an ongoing relationship to distribute such manufacturer’s
products, and
(B) the term ‘‘wholesale distribution’’ means distribution of drugs subject to subsection (b) to
other than the consumer or patient but does not include intracompany sales and does not
include distributions of drugs described in subsection (c)(3)(B).
(f)(1)(A) A drug intended for use by animals other than man, other than a veterinary feed
directive drug intended for use in animal feed or an animal feed bearing or containing a
veterinary feed directive drug, which—
(i) because of its toxicity or other potentiality for harmful effect, or the method of its use, or the
collateral measures necessary for its use, is not safe for animal use except under the
professional supervision of a licensed veterinarian, or
(ii) is limited by an approved application under subsection (b) of section 512, a
conditionally-approved application under section 571, or an index listing under section 572 to
use under the professional supervision of a licensed veterinarian, shall be dispensed only by
or upon the lawful written or oral order of a licensed veterinarian in the course of the
veterinarian’s professional practice.
(B) For purposes of subparagraph (A), an order is lawful if the order—
(i) is a prescription or other order authorized by law,
(ii) is, if an oral order, promptly reduced to writing by the person lawfully filling the order, and
filed by that person, and
(iii) is refilled only if authorized in the original order or in a subsequent oral order promptly
reduced to writing by the person lawfully filling the order, and filed by that person.
(C) The act of dispensing a drug contrary to the provisions of this paragraph shall be deemed
to be an act which results in the drug being misbranded while held for sale.
(2) Any drug when dispensed in accordance with paragraph (1) of this subsection—
(A) Shall be exempt from the requirements of section 502, except subsections (a), (g), (h),
(i)(2), (i)(3), and (p) of such section, and
(B) shall be exempt from the packaging requirements of subsections (g), (h), and (p) of such
section, if—
(i) when dispensed by a licensed veterinarian, the drug bears a label containing the name and
address of the practitioner and any directions for use and cautionary statements specified by
the practitioner, or
(ii) when dispensed by filling the lawful order of a licensed veterinarian, the drug bears a label
containing the name and address of the dispenser, the serial number and date of the order or
of its filing, the name of the licensed veterinarian, and the directions for use and cautionary
statements, if any, contained in such order.
The preceding sentence shall not apply to any drug dispensed in the course of the conduct of
a business of dispensing drugs pursuant to diagnosis by mail.
(3) The Secretary may by regulation exempt drugs for animals other than man subject to
section 512, 571, or 572 from the requirements of paragraph (1) when such requirements are
not necessary for the protection of the public health.
(4) A drug which is subject to paragraph (1) shall be deemed to be misbranded if at any time
prior to dispensing its label fails to bear the statement ‘‘Caution: Federal law restricts this drug
to use by or on the order of a licensed veterinarian.’’. A drug to which paragraph (1) does not
apply shall be deemed to be misbranded if at any time prior to dispensing its label bears the
statement specified in the preceding sentence.
(g)(1) The Secretary shall in accordance with this subsection assign an agency center to
regulate products that constitute a combination of a drug, device, or biological product. The
Secretary shall determine the primary mode of action of the combination product. If the
Secretary determines that the primary mode of action is that of—
(A) a drug (other than a biological product), the agency center charged with premarket review
of drugs shall have primary jurisdiction,
(B) a device, the agency center charged with premarket review of devices shall have primary
jurisdiction, or
(C) a biological product, the agency center charged with premarket review of biological
products shall have primary jurisdiction.
(2) Nothing in this subsection shall prevent the Secretary from using any agency resources of
the Food and Drug Administration necessary to ensure adequate review of the safety,
effectiveness, or substantial equivalence of an article.
(3) The Secretary shall promulgate regulations to implement market clearance procedures in
accordance with paragraphs (1) and (2) not later than 1 year after the date of enactment of this
subsection. 11
(4) (A) Not later than 60 days after the date of the enactment of this paragraph 12, the
Secretary shall establish within the Office of the Commissioner of Food and Drugs an office to
ensure the prompt assignment of combination products to agency centers, the timely and
effective premarket review of such products, and consistent and appropriate postmarket
regulation of like products subject to the same statutory requirements to the extent permitted
by law. Additionally, the office shall, in determining whether a product is to be designated a
combination product, consult with the component within the Office of the Commissioner of
Food and Drugs that is responsible for such determinations. Such office (referred to in this
paragraph as the `Office') shall have appropriate scientific and medical expertise, and shall be
headed by a director.
(B) In carrying out this subsection, the Office shall, for each combination product, promptly
assign an agency center with primary jurisdiction in accordance with paragraph (1) for the
premarket review of such product.
(C)(i) In carrying out this subsection, the Office shall ensure timely and effective premarket
reviews by overseeing the timeliness of and coordinating reviews involving more than one
agency center.
(ii) In order to ensure the timeliness of the premarket review of a combination product, the
agency center with primary jurisdiction for the product, and the consulting agency center, shall
be responsible to the Office with respect to the timeliness of the premarket review.
(D) In carrying out this subsection, the Office shall ensure the consistency and
appropriateness of postmarket regulation of like products subject to the same statutory
requirements to the extent permitted by law.
(E)(i) Any dispute regarding the timeliness of the premarket review of a combination product
may be presented to the Office for resolution, unless the dispute is clearly premature.
(ii) During the review process, any dispute regarding the substance of the premarket review
may be presented to the Commissioner of Food and Drugs after first being considered by the
agency center with primary jurisdiction of the premarket review, under the scientific dispute
resolution procedures for such center. The Commissioner of Food and Drugs shall consult with
the Director of the Office in resolving the substantive dispute.
(F) The Secretary, acting through the Office, shall review each agreement, guidance, or
practice of the Secretary that is specific to the assignment of combination products to agency
centers and shall determine whether the agreement, guidance, or practice is consistent with
the requirements of this subsection. In carrying out such review, the Secretary shall consult
with stakeholders and the directors of the agency centers. <> After such consultation, the
Secretary shall determine whether to continue in effect, modify, revise, or eliminate such
agreement, guidance, or practice, and shall publish in the Federal Register a notice of the
availability of such modified or revised agreement, guidance or practice. Nothing in this
paragraph shall be construed as preventing the Secretary from following each agreement,
guidance, or practice until continued, modified, revised, or eliminated.
(G) Not later than one year after the date of the enactment of this paragraph and annually
thereafter, the Secretary shall report to the appropriate committees of Congress on the
activities and impact of the Office. The report shall include provisions--
(i) describing the numbers and types of combination products under review and the timeliness
in days of such assignments, reviews, and dispute resolutions;
(ii) identifying the number of premarket reviews of such products that involved a consulting
agency center; and
(iii) describing improvements in the consistency of postmarket regulation of combination
products.
(H) Nothing in this paragraph shall be construed to limit the regulatory authority of any agency
center.
(5) As used in this subsection:
(A) The term `agency center' means a center or alternative organizational component of the
Food and Drug Administration.
(B) The term ‘‘biological product’’ has the meaning given the term in section 351(i) of the Public
Health Service Act (42 U.S.C. 262(i)).
(C) The term ‘‘market clearance’’ includes—
(i) approval of an application under section 505, 507, 515, or 520(g),
(ii) a finding of substantial equivalence under this subchapter, and
(iii) approval of a biologics license application under subsection (a) of section 351 of the Public
Health Service Act (42 U.S.C. 262).
SEC. 503A. [ 21 U.S.C. 353a] PHARMACY COMPOUNDING.
(a) IN GENERAL.—Sections 501(a)(2)(B), 502(f)(1), and 505 shall not apply to a drug product
if the drug product is compounded for an identified individual patient based on the unsolicited
receipt of a valid prescription order or a notation, approved by the prescribing practitioner, on
the prescription order that a compounded product is necessary for the identified patient, if the
drug product meets the requirements of this section, and if the compounding—
(1) is by—
(A) a licensed pharmacist in a State licensed pharmacy or a Federal facility, or
(B) a licensed physician, on the prescription order for such individual patient made by a
licensed physician or other licensed practitioner authorized by State law to prescribe drugs; or
(2)(A) is by a licensed pharmacist or licensed physician in limited quantities before the receipt
of a valid prescription order for such individual patient; and
(B) is based on a history of the licensed pharmacist or licensed physician receiving valid
prescription orders for the compounding of the drug product, which orders have been
generated solely within an established relationship between—
(i) the licensed pharmacist or licensed physician; and
(ii)(I) such individual patient for whom the prescription order will be provided; or
(II) the physician or other licensed practitioner who will write such prescription order.
(b) COMPOUNDED DRUG.—
(1) LICENSED PHARMACIST AND LICENSED PHYSICIAN.—A drug product may be
compounded under subsection (a) if the licensed pharmacist or licensed physician—
(A) compounds the drug product using bulk drug substances, as defined in regulations of the
Secretary published at section 207.3(a)(4) of title 21 of the Code of Federal Regulations—
(i) that—
(I) comply with the standards of an applicable United States Pharmacopoeia or National
Formulary monograph, if a monograph exists, and the United States Pharmacopoeia chapter
on pharmacy compounding;
(II) if such a monograph does not exist, are drug substances that are components of drugs
approved by the Secretary; or
(III) if such a monograph does not exist and the drug substance is not a component of a drug
approved by the Secretary, that appear on a list developed by the Secretary through
regulations issued by the Secretary under subsection (d);
(ii) that are manufactured by an establishment that is registered under section 510 (including a
foreign establishment that is registered under section 510(i)); and
(iii) that are accompanied by valid certificates of analysis for each bulk drug substance;
(B) compounds the drug product using ingredients (other than bulk drug substances) that
comply with the standards of an applicable United States Pharmacopoeia or National
Formulary monograph, if a monograph exists, and the United States Pharmacopoeia chapter
on pharmacy compounding;
(C) does not compound a drug product that appears on a list published by the Secretary in the
Federal Register of drug products that have been withdrawn or removed from the market
because such drug products or components of such drug products have been found to be
unsafe or not effective; and
(D) does not compound regularly or in inordinate amounts (as defined by the Secretary) any
drug products that are essentially copies of a commercially available drug product.
(2) DEFINITION.—For purposes of paragraph (1)(D), the term ‘‘essentially a copy of a
commercially available drug product’’ does not include a drug product in which there is a
change, made for an identified individual patient, which produces for that patient a significant
difference, as determined by the prescribing practitioner, between the compounded drug and
the comparable commercially available drug product.
(3) DRUG PRODUCT.—A drug product may be compounded under subsection (a) only if—
(A) such drug product is not a drug product identified by the Secretary by regulation as a drug
product that presents demonstrable difficulties for compounding that reasonably demonstrate
an adverse effect on the safety or effectiveness of that drug product; and
(B) such drug product is compounded in a State—
(i) that has entered into a memorandum of understanding with the Secretary which addresses
the distribution of inordinate amounts of compounded drug products interstate and provides for
appropriate investigation by a State agency of complaints relating to compounded drug
products distributed outside such State; or
(ii) that has not entered into the memorandum of understanding described in clause (i) and the
licensed pharmacist, licensed pharmacy, or licensed physician distributes (or causes to be
distributed) compounded drug products out of the State in which they are compounded in
quantities that do not exceed 5 percent of the total prescription orders dispensed or distributed
by such pharmacy or physician.
The Secretary shall, in consultation with the National Association of Boards of Pharmacy,
develop a standard memorandum of understanding for use by the States in complying with
subparagraph (B)(i).
(c) ADVERTISING AND PROMOTION.—A drug may be compounded under subsection (a)
only if the pharmacy, licensed pharmacist, or licensed physician does not advertise or promote
the compounding of any particular drug, class of drug, or type of drug. The pharmacy, licensed
pharmacist, or licensed physician may advertise and promote the compounding service
provided by the licensed pharmacist or licensed physician.
(d) REGULATIONS.—
(1) IN GENERAL.—The Secretary shall issue regulations to implement this section. Before
issuing regulations to implement subsections (b)(1)(A)(i)(III), (b)(1)(C), or (b)(3)(A), the
Secretary shall convene and consult an advisory committee on compounding unless the
Secretary determines that the issuance of such regulations before consultation is necessary to
protect the public health. The advisory committee shall include representatives from the
National Association of Boards of Pharmacy, the United States Pharmacopoeia, pharmacy,
physician, and consumer organizations, and other experts selected by the Secretary.
(2) LIMITING COMPOUNDING.—The Secretary, in consultation with the United States
Pharmacopoeia Convention, Incorporated, shall promulgate regulations identifying drug
substances that may be used in compounding under subsection (b)(1)(A)(i)(III) for which a
monograph does not exist or which are not components of drug products approved by the
Secretary. The Secretary shall include in the regulation the criteria for such substances, which
shall include historical use, reports in peer reviewed medical literature, or other criteria the
Secretary may identify.
(e) APPLICATION.—This section shall not apply to—
(1) compounded positron emission tomography drugs as defined in section 201(ii); or
(2) radiopharmaceuticals.
(f) DEFINITION.—As used in this section, the term ‘‘compounding’’ does not include mixing,
reconstituting, or other such acts that are performed in accordance with directions contained in
approved labeling provided by the product’s manufacturer and other manufacturer directions
consistent with that labeling.
VETERINARY FEED DIRECTIVE DRUGS
SEC. 504. [21 U.S.C. 354] (a)(1) A drug intended for use in or on animal feed which is limited
by an approved application filed pursuant to section 512(b), a conditionally-approved
application filed pursuant to section 571, or an index listing pursuant to section 572 to use
under the professional supervision of a licensed veterinarian is a veterinary feed directive drug.
Any animal feed bearing or containing a veterinary feed directive drug shall be fed to animals
only by or upon a lawful veterinary feed directive issued by a licensed veterinarian in the
course of the veterinarian’s professional practice. When labeled, distributed, held, and used in
accordance with this section, a veterinary feed directive drug and any animal feed bearing or
containing a veterinary feed directive drug shall be exempt from section 502(f).
(2) A veterinary feed directive is lawful if it—
(A) contains such information as the Secretary may by general regulation or by order require;
and
(B) is in compliance with the conditions and indications for use of the drug set forth in the
notice published pursuant to section 512(i), or the index listing pursuant to section 572(e).
(3)(A) Any persons involved in the distribution or use of animal feed bearing or containing a
veterinary feed directive drug and the licensed veterinarian issuing the veterinary feed
directive shall maintain a copy of the veterinary feed directive applicable to each such feed,
except in the case of a person distributing such feed to another person for further distribution.
Such person distributing the feed shall maintain a written acknowledgment from the person to
whom the feed is shipped stating that that person shall not ship or move such feed to an
animal production facility without a veterinary feed directive or ship such feed to another
person for further distribution unless that person has provided the same written
acknowledgment to its immediate supplier.
(B) Every person required under subparagraph (A) to maintain records, and every person in
charge or custody thereof, shall, upon request of an officer or employee designated by the
Secretary, permit such officer or employee at all reasonable times to have access to and copy
and verify such records.
(C) Any person who distributes animal feed bearing or containing a veterinary feed directive
drug shall upon first engaging in such distribution notify the Secretary of that person’s name
and place of business. The failure to provide such notification shall be deemed to be an act
which results in the drug being misbranded.
(b) A veterinary feed directive drug and any feed bearing or containing a veterinary feed
directive drug shall be deemed to be misbranded if their labeling fails to bear such cautionary
statement and such other information as the Secretary may by general regulation or by order
prescribe, or their advertising fails to conform to the conditions and indications for use
published pursuant to section 512(i), or the index listing pursuant to section 572(e) or fails to
contain the general cautionary statement prescribed by the Secretary.
(c) Neither a drug subject to this section, nor animal feed bearing or containing such a drug,
shall be deemed to be a prescription article under any Federal or State law.
NEW DRUGS
SEC. 505. [21 U.S.C. 355] (a) No person shall introduce or deliver for introduction into
interstate commerce any new drug, unless an approval of an application filed pursuant to
subsection (b) or (j) is effective with respect to such drug.
(b)(1) Any person may file with the Secretary an application with respect to any drug subject to
the provisions of subsection (a). Such persons shall submit to the Secretary as a part of the
application (A) full reports of investigations which have been made to show whether or not
such drug is safe for use and whether such drug is effective in use; 13 (B) a full list of the
articles used as components of such drug; (C) a full statement of the composition of such drug;
(D) a full description of the methods used in, and the facilities and controls used for, the
manufacture, processing, and packing of such drug; (E) such samples of such drug and of the
articles used as components thereof as the Secretary may require; (F) specimens of the
labeling proposed to be used for such drug and (G) any assessments required under section
505B. The applicant shall file with the application the patent number and the expiration date of
any patent which claims the drug for which the applicant submitted the application or which
claims a method of using such drug and with respect to which a claim of patent infringement
could reasonably be asserted if a person not licensed by the owner engaged in the
manufacture use, or sale of the drug. If a application is filed under this subsection for a drug
and a patent which claims such drug or a method of using such drug is issued after the filing
date but before approval of the application, the applicant shall amend the application to include
the information required by the preceding sentence. Upon approval of the application, the
Secretary shall publish information submitted under the two preceding sentences. The
Secretary shall, in consultation with the Director of the National Institutes of Health and with
representatives of the drug manufacturing industry, review and develop guidance, as
appropriate, on the inclusion of women and minorities in clinical trials required by clause (A).
(2) An application submitted under paragraph (1) for a drug for which the investigations
described in clause (A) of such paragraph and relied upon by the applicant for approval of the
application were not conducted by or for the applicant and for which the applicant has not
obtained a right of reference or use from the person by or for whom the investigations were
conducted shall also include—
(A) a certification, in the opinion of the applicant and to the best of his knowledge, with respect
to each patent which claims the drug for which such investigations were conducted or which
claims a use for such drug for which the applicant is seeking approval under this subsection
and for which information is required to be filed under paragraph (1) or subsection (c)—
(i) that such patent information has not been filed,
(ii) that such patent has expired,
(iii) of the date on which such patent will expire, or
(iv) that such patent is invalid or will not be infringed by the manufacture, use, or sale of the
new drug for which the application is submitted; and
(B) if with respect to the drug for which investigations described in paragraph (1)(A) were
conducted information was filed under paragraph (1) or subsection (c) for a method of use
patent which does not claim a use for which the applicant is seeking approval under this
subsection, a statement that the method of use patent does not claim such a use.
(3) Notice of opinion that patent is invalid or will not be infringed.--
(A) Agreement to give notice.--An applicant that makes a certification described in paragraph
(2)(A)(iv) shall include in the application a statement that the applicant will give notice as
required by this paragraph.
(B) Timing of notice.--An applicant that makes a certification described in paragraph (2)(A)(iv)
shall give notice as required under this paragraph--
(i) if the certification is in the application, not later than 20 days after the date of the postmark
on the notice with which the Secretary informs the applicant that the application has been filed;
or
(ii) if the certification is in an amendment or supplement to the application, at the time at which
the applicant submits the amendment or supplement, regardless of whether the applicant has
already given notice with respect to another such certification contained in the application or in
an amendment or supplement to the application.
(C) Recipients of notice.--An applicant required under this paragraph to give notice shall give
notice to--
(i) each owner of the patent that is the subject of the certification (or a representative of the
owner designated to receive such a notice); and
(ii) the holder of the approved application under this subsection for the drug that is claimed by
the patent or a use of which is claimed by the patent (or a representative of the holder
designated to receive such a notice).
(D) Contents of notice.--A notice required under this paragraph shall--
(i) state that an application that contains data from bioavailability or bioequivalence studies has
been submitted under this subsection for the drug with respect to which the certification is
made to obtain approval to engage in the commercial manufacture, use, or sale of the drug
before the expiration of the patent referred to in the certification; and
(ii) include a detailed statement of the factual and legal basis of the opinion of the applicant
that the patent is invalid or will not be infringed.
(4)(A) An applicant may not amend or supplement an application referred to in paragraph (2)
to seek approval of a drug that is a different drug than the drug identified in the application as
submitted to the Secretary.
(B) With respect to the drug for which such an application is submitted, nothing in this
subsection or subsection (c)(3) prohibits an applicant from amending or supplementing the
application to seek approval of a different strength.
( 5)(A) The Secretary shall issue guidance for the individuals who review applications
submitted under paragraph (1) or under section 351 of the Public Health Service Act, which
shall relate to promptness in conducting the review, technical excellence, lack of bias and
conflict of interest, and knowledge of regulatory and scientific standards, and which shall apply
equally to all individuals who review such applications.
(B) The Secretary shall meet with a sponsor of an investigation or an applicant for approval for
a drug under this subsection or section 351 of the Public Health Service Act if the sponsor or
applicant makes a reasonable written request for a meeting for the purpose of reaching
agreement on the design and size of clinical trials intended to form the primary basis of an
effectiveness claim. The sponsor or applicant shall provide information necessary for
discussion and agreement on the design and size of the clinical trials. Minutes of any such
meeting shall be prepared by the Secretary and made available to the sponsor or applicant
upon request.
(C) Any agreement regarding the parameters of the design and size of clinical trials of a new
drug under this paragraph that is reached between the Secretary and a sponsor or applicant
shall be reduced to writing and made part of the administrative record by the Secretary. Such
agreement shall not be changed after the testing begins, except—
(i) with the written agreement of the sponsor or applicant; or
(ii) pursuant to a decision, made in accordance with subparagraph (D) by the director of the
reviewing division, that a substantial scientific issue essential to determining the safety or
effectiveness of the drug has been identified after the testing has begun.
(D) A decision under subparagraph (C)(ii) by the director shall be in writing and the Secretary
shall provide to the sponsor or applicant an opportunity for a meeting at which the director and
the sponsor or applicant will be present and at which the director will document the scientific
issue involved.
(E) The written decisions of the reviewing division shall be binding upon, and may not directly
or indirectly be changed by, the field or compliance division personnel unless such field or
compliance division personnel demonstrate to the reviewing division why such decision should
be modified.
(F) No action by the reviewing division may be delayed because of the unavailability of
information from or action by field personnel unless the reviewing division determines that a
delay is necessary to assure the marketing of a safe and effective drug.
(G) For purposes of this paragraph, the reviewing division is the division responsible for the
review of an application for approval of a drug under this subsection or section 351 of the
Public Health Service Act (including all scientific and medical matters, chemistry,
manufacturing, and controls).
(c)(1) Within one hundred and eighty days after the filing of an application under subsection (b),
or such additional period as may be agreed upon by the Secretary and the applicant, the
Secretary shall either—
(A) approve the application if he then finds that none of the grounds for denying approval
specified in subsection (d) applies, or
(B) give the applicant notice of an opportunity for a hearing before the Secretary under
subsection (d) on the question whether such application is approvable. If the applicant elects
to accept the opportunity for hearing by written request within thirty days after such notice,
such hearing shall commence not more than ninety days after the expiration of such thirty days
unless the Secretary and the applicant otherwise agree. Any such hearing shall thereafter be
conducted on an expedited basis and the Secretary’s order thereon shall be issued within
ninety days after the date fixed by the Secretary for filing final briefs.
(2) If the patent information described in subsection (b) could not be filed with the submission
of an application under subsection (b) because the application was filed before the patent
information was required under subsection (b) or a patent was issued after the application was
approved under such subsection, the holder of an approved application shall file with the
Secretary, the patent number and the expiration date of any patent which claims the drug for
which the application was submitted or which claims a method of using such drug and with
respect to which a claim of patent infringement could reasonably be asserted if a person not
licensed by the owner engaged in the manufacture, use, or sale of the drug. If the holder of an
approved application could not file patent information under subsection (b) because it was not
required at the time the application was approved, the holder shall file such information under
this subsection not later than thirty days after the date of the enactment of this sentence 14,
and if the holder of an approved application could not file patent information under subsection
(b) because no patent had been issued when an application was filed or approved, the holder
shall file such information under this subsection not later than thirty days after the date the
patent involved is issued. Upon the submission of patent information under this subsection, the
Secretary shall publish it.
(3) The approval of an application filed under subsection (b) which contains a certification
required by paragraph (2) of such subsection shall be made effective on the last applicable
date determined by applying the following to each certification made under subsection
(b)(2)(A):
(A) If the applicant only made a certification described in clause (i) or (ii) of subsection (b)(2)(A)
or in both such clauses, the approval may be made effective immediately.
(B) If the applicant made a certification described in clause (iii) of subsection (b)(2)(A), the
approval may be made effective on the date certified under clause (iii).
(C) If the applicant made a certification described in clause (iv) of subsection (b)(2)(A), the
approval shall be made effective immediately unless, before the expiration of 45 days after the
date on which the notice described in subsection (b)(3) is received, an action is brought for
infringement of the patent that is the subject of the certification and for which information was
submitted to the Secretary under paragraph (2) or subsection (b)(1) before the date on which
the application (excluding an amendment or supplement to the application) was submitted. If
such an action is brought before the expiration of such days, the approval may be made
effective upon the expiration of the thirty-month period beginning on the date of the receipt of
the notice provided under subsection (b)(3) or such shorter or longer period as the court may
order because either party to the action failed to reasonably cooperate in expediting the action,
except that—
(i) if before the expiration of such period the district court decides that the patent is invalid or
not infringed (including any substantive determination that there is no cause of action for
patent infringement or invalidity), the approval shall be made effective on--
(I) the date on which the court enters judgment reflecting the decision; or
(II) the date of a settlement order or consent decree signed and entered by the court stating
that the patent that is the subject of the certification is invalid or not infringed;
(ii) if before the expiration of such period the district court decides that the patent has been
infringed--
(I) if the judgment of the district court is appealed, the approval shall be made effective on--
(aa) the date on which the court of appeals decides that the patent is invalid or not infringed
(including any substantive determination that there is no cause of action for patent
infringement or invalidity); or
(bb) the date of a settlement order or consent decree signed and entered by the court of
appeals stating that the patent that is the subject of the certification is invalid or not infringed;
or
(II) if the judgment of the district court is not appealed or is affirmed, the approval shall be
made effective on the date specified by the district court in a court order under section
271(e)(4)(A) of title 35, United States Code;
(iii) if before the expiration of such period the court grants a preliminary injunction prohibiting
the applicant from engaging in the commercial manufacture or sale of the drug until the court
decides the issues of patent validity and infringement and if the court decides that such patent
is invalid or not infringed, the approval shall be made effective as provided in clause (i); or
(iv) if before the expiration of such period the court grants a preliminary injunction prohibiting
the applicant from engaging in the commercial manufacture or sale of the drug until the court
decides the issues of patent validity and infringement and if the court decides that such patent
has been infringed, the approval shall be made effective as provided in clause (ii).
In such an action, each of the parties shall reasonably cooperate in expediting the action.
(D) Civil action to obtain patent certainty.—
(i) Declaratory judgment absent infringement action.--
(I) In general.--No action may be brought under section 2201 of title 28, United States Code,
by an applicant referred to in subsection (b)(2) for a declaratory judgment with respect to a
patent which is the subject of the certification referred to in subparagraph (C) unless--
(aa) the 45-day period referred to in such subparagraph has expired;
(bb) neither the owner of such patent nor the holder of the approved application under
subsection (b) for the drug that is claimed by the patent or a use of which is claimed by the
patent brought a civil action against the applicant for infringement of the patent before the
expiration of such period; and
(cc) in any case in which the notice provided under paragraph (2)(B) 15 relates to
noninfringement, the notice was accompanied by a document described in subclause (III).
(II) Filing of civil action.--If the conditions described in items (aa), (bb), and as applicable, (cc)
of subclause (I) have been met, the applicant referred to in such subclause may, in
accordance with section 2201 of title 28, United States Code, bring a civil action under such
section against the owner or holder referred to in such subclause (but not against any owner or
holder that has brought such a civil action against the applicant, unless that civil action was
dismissed without prejudice) for a declaratory judgment that the patent is invalid or will not be
infringed by the drug for which the applicant seeks approval, except that such civil action may
be brought for a declaratory judgment that the patent will not be infringed only in a case in
which the condition described in subclause (I)(cc) is applicable. A civil action referred to in this
subclause shall be brought in the judicial district where the defendant has its principal place of
business or a regular and established place of business.
(III) Offer of confidential access to application.--For purposes of subclause (I)(cc), the
document described in this subclause is a document providing an offer of confidential access
to the application that is in the custody of the applicant referred to in subsection (b)(2) for the
purpose of determining whether an action referred to in subparagraph (C) should be brought.
The document providing the offer of confidential access shall contain such restrictions as to
persons entitled to access, and on the use and disposition of any information accessed, as
would apply had a protective order been entered for the purpose of protecting trade secrets
and other confidential business information. A request for access to an application under an
offer of confidential access shall be considered acceptance of the offer of confidential access
with the restrictions as to persons entitled to access, and on the use and disposition of any
information accessed, contained in the offer of confidential access, and those restrictions and
other terms of the offer of confidential access shall be considered terms of an enforceable
contract. Any person provided an offer of confidential access shall review the application for
the sole and limited purpose of evaluating possible infringement of the patent that is the
subject of the certification under subsection (b)(2)(A)(iv) and for no other purpose, and may not
disclose information of no relevance to any issue of patent infringement to any person other
than a person provided an offer of confidential access. Further, the application may be
redacted by the applicant to remove any information of no relevance to any issue of patent
infringement.
(ii) Counterclaim to infringement action.—
(I) In general.--If an owner of the patent or the holder of the approved application under
subsection (b) for the drug that is claimed by the patent or a use of which is claimed by the
patent brings a patent infringement action against the applicant, the applicant may assert a
counterclaim seeking an order requiring the holder to correct or delete the patent information
submitted by the holder under subsection (b) or this subsection on the ground that the patent
does not claim either--
(aa) the drug for which the application was approved; or
(bb) an approved method of using the drug.
(II) No independent cause of action.--Subclause (I) does not authorize the assertion of a claim
described in subclause (I) in any civil action or proceeding other than a counterclaim described
in subclause (I).
(iii) No damages.--An applicant shall not be entitled to damages in a civil action under clause (i)
or a counterclaim under clause (ii).
( E)(i) If an application (other than an abbreviated new drug application) submitted under
subsection (b) for a drug, no active ingredient (including any ester or salt of the active
ingredient) of which has been approved in any other application under subsection (b), was
approved during the period beginning January 1, 1982, and ending on the date of the
enactment of this subsection 16, the Secretary may not make the approval of another
application for a drug for which the investigations described in clause (A) of subsection (b)(1)
and relied upon by the applicant for approval of the application were not conducted by or for
the applicant and for which the applicant has not obtained a right of reference or use from the
person by or for whom the investigations were conducted effective before the expiration of ten
years from the date of the approval of the application previously approved under subsection
(b).
(ii) If an application submitted under subsection (b) for a drug, no active ingredient (including
any ester or salt of the active ingredient) of which has been approved in any other application
under subsection (b), is approved after the date of the enactment of this clause, no application
which refers to the drug for which the subsection (b) application was submitted and for which
the investigations described in clause (A) of subsection (b)(1) and relied upon by the applicant
for approval of the application were not conducted by or for the applicant and for which the
applicant has not obtained a right of reference or use from the person by or for whom the
investigations were conducted may be submitted under subsection (b) before the expiration of
five years from the date of the approval of the application under subsection (b), except that
such an application may be submitted under subsection (b) after the expiration of four years
from the date of the approval of the subsection (b) application if it contains a certification of
patent invalidity or noninfringement described in clause (iv) of subsection (b)(2)(A). The
approval of such an application shall be made effective in accordance with this paragraph
except that, if an action for patent infringement is commenced during the one-year period
beginning forty-eight months after the date of the approval of the subsection (b) application,
the thirty-month period referred to in subparagraph (C) shall be extended by such amount of
time (if any) which is required for seven and one-half years to have elapsed from the date of
approval of the subsection (b) application.
(iii) If an application submitted under subsection (b) for a drug, which includes an active
ingredient (including any ester or salt of the active ingredient) that has been approved in
another application approved under subsection (b), is approved after the date of the
enactment of this clause and if such application contains reports of new clinical investigations
(other than bioavailability studies) essential to the approval of the application and conducted or
sponsored by the applicant, the Secretary may not make the approval of an application
submitted under subsection (b) for the conditions of approval of such drug in the approved
subsection (b) application effective before the expiration of three years from the date of the
approval of the application under subsection (b) if the investigations described in clause (A) of
subsection (b)(1) and relied upon by the applicant for approval of the application were not
conducted by or for the applicant and if the applicant has not obtained a right of reference or
use from the person by or for whom the investigations were conducted.
(iv) If a supplement to an application approved under subsection (b) is approved after the date
of enactment of this clause and the supplement contains reports of new clinical investigations
(other than bioavailabilty 17 studies) essential to the approval of the supplement and
conducted or sponsored by the person submitting the supplement, the Secretary may not
make the approval of an application submitted under subsection (b) for a change approved in
the supplement effective before the expiration of three years from the date of the approval of
the supplement under subsection (b) if the investigations described in clause (A) of subsection
(b)(1) and relied upon by the applicant for approval of the application were not conducted by or
for the applicant and if the applicant has not obtained a right of reference or use from the
person by or for whom the investigations were conducted.
(v) If an application (or supplement to an application) submitted under subsection (b) for a drug,
which includes an active ingredient (including any ester or salt of the active ingredient) that has
been approved in another application under subsection (b), was approved during the period
beginning January 1, 1982, and ending on the date of the enactment of this clause, the
Secretary may not make the approval of an application submitted under this subsection and for
which the investigations described in clause (A) of subsection (b)(1) and relied upon by the
applicant for approval of the application were not conducted by or for the applicant and for
which the applicant has not obtained a right of reference or use from the person by or for
whom the investigations were conducted and which refers to the drug for which the subsection
(b) application was submitted effective before the expiration of two years from the date of
enactment of this clause.
(4) A drug manufactured in a pilot or other small facility may be used to demonstrate the safety
and effectiveness of the drug and to obtain approval for the drug prior to manufacture of the
drug in a larger facility, unless the Secretary makes a determination that a full scale production
facility is necessary to ensure the safety or effectiveness of the drug.
(d) If the Secretary finds, after due notice to the applicant in accordance with subsection (c)
and giving him an opportunity for a hearing, in accordance with said subsection, that (1) the
investigations, reports of which are required to be submitted to the Secretary pursuant to
subsection (b), do not include adequate tests by all methods reasonably applicable to show
whether or not such drug is safe for use under the conditions prescribed, recommended, or
suggested in the proposed labeling thereof; (2) the results of such tests show that such drug is
unsafe for use under such conditions or do not show that such drug is safe for use under such
conditions; (3) the methods used in, and the facilities and controls used for, the manufacture,
processing, and packing of such drug are inadequate to preserve its identity, strength, quality,
and purity; (4) upon the basis of the information submitted to him as part of the application, or
upon the basis of any other information before him with respect to such drug, he has
insufficient information to determine whether such drug is safe for use under such conditions;
or (5) evaluated on the basis of the information submitted to him as part of the application and
any other information before him with respect to such drug, there is a lack of substantial
evidence that the drug will have the effect it purports or is represented to have under the
conditions of use prescribed, recommended, or suggested in the proposed labeling thereof; or
(6) the application failed to contain the patent information prescribed by subsection (b); or (7)
based on a fair evaluation of all material facts, such labeling is false or misleading in any
particular; he shall issue an order refusing to approve the application. If, after such notice and
opportunity for hearing, the Secretary finds that clauses (1) through (6) do not apply, he shall
issue an order approving the application. As used in this subsection and subsection (e), the
term ‘‘substantial evidence’’ means evidence consisting of adequate and well-controlled
investigations, including clinical investigations, by experts qualified by scientific training and
experience to evaluate the effectiveness of the drug involved, on the basis of which it could
fairly and responsibly be concluded by such experts that the drug will have the effect it
purports or is represented to have under the conditions of use prescribed, recommended, or
suggested in the labeling or proposed labeling thereof. If the Secretary determines, based on
relevant science, that data from one adequate and well-controlled clinical investigation and
confirmatory evidence (obtained prior to or after such investigation) are sufficient to establish
effectiveness, the Secretary may consider such data and evidence to constitute substantial
evidence for purposes of the preceding sentence.
(e) The Secretary shall, after due notice and opportunity for hearing to the applicant, withdraw
approval of an application with respect to any drug under this section if the Secretary finds (1)
that clinical or other experience, tests, or other scientific data show that such drug is unsafe for
use under the conditions of use upon the basis of which the application was approved; (2) that
new evidence of clinical experience, not contained in such application or not available to the
Secretary until after such application was approved, or tests by new methods, or tests by
methods not deemed reasonably applicable when such application was approved, evaluated
together with the evidence available to the Secretary when the application was approved,
shows that such drug is not shown to be safe for use under the conditions of use upon the
basis of which the application was approved; or (3) on the basis of new information before him
with respect to such drug, evaluated together with the evidence available to him when the
application was approved, that there is a lack of substantial evidence that the drug will have
the effect it purports or is represented to have under the conditions of use prescribed,
recommended, or suggested in the labeling thereof; or (4) the patent information prescribed by
subsection (c) was not filed within thirty days after the receipt of written notice from the
Secretary specifying the failure to file such information; or (5) that the application contains any
untrue statement of a material fact: Provided, That if the Secretary (or in his absence the
officer acting as Secretary) finds that there is an imminent hazard to the public health, he may
suspend the approval of such application immediately, and give the applicant prompt notice of
his action and afford the applicant the opportunity for an expedited hearing under this
subsection; but the authority conferred by this proviso to suspend the approval of an
application shall not be delegated. The Secretary may also, after due notice and opportunity
for hearing to the applicant, withdraw the approval of an application submitted under
subsection (b) or (j) with respect to any drug under this section if the Secretary finds (1) that
the applicant has failed to establish a system for maintaining required records, or has
repeatedly or deliberately failed to maintain such records or to make required reports, in
accordance with a regulation or order under subsection (k) or to comply with the notice
requirements of section 510(k)(2), or the applicant has refused to permit access to, or copying
or verification of, such records as required by paragraph (2) of such subsection; or (2) that on
the basis of new information before him, evaluated together with the evidence before him
when the application was approved, the methods used in, or the facilities and controls used for,
the manufacture, processing, and packing of such drug are inadequate to assure and preserve
its identity, strength, quality, and purity and were not made adequate within a reasonable time
after receipt of written notice from the Secretary specifying the matter complained of; or (3)
that on the basis of new information before him, evaluated together with the evidence before
him when the application was approved, the labeling of such drug, based on a fair evaluation
of all material facts, is false or misleading in any particular and was not corrected within a
reasonable time after receipt of written notice from the Secretary specifying the matter
complained of. Any order under this subsection shall state the findings upon which it is based.
(f) Whenever the Secretary finds that the facts so require, he shall revoke any previous order
under subsection (d) or (e) refusing, withdrawing, or suspending approval of an application
and shall approve such application or reinstate such approval, as may be appropriate.
(g) Orders of the Secretary issued under this section shall be served (1) in person by any
officer or employee of the Department designated by the Secretary or (2) by mailing the order
by registered mail or by certified mail addressed to the applicant or respondent at his
last-known address in the records of the Secretary.
(h) An appeal may be taken by the applicant from an order of the Secretary refusing or
withdrawing approval of an application under this section. Such appeal shall be taken by filing
in the United States court of appeals for the circuit wherein such applicant resides or has his
principal place of business, or in the United States Court of Appeals for the District of Columbia
Circuit, within sixty days after the entry of such order, a written petition praying that the order of
the Secretary be set aside. A copy of such petition shall be forthwith transmitted by the clerk of
the court to the Secretary, or any officer designated by him for that purpose, and thereupon the
Secretary shall certify and file in the court the record upon which the order complained of was
entered, as provided in section 2112 of title 28, United States Code. Upon the filing of such
petition such court shall have exclusive jurisdiction to affirm or set aside such order, except
that until the filing of the record the Secretary may modify or set aside his order. No objection
to the order of the Secretary shall be considered by the court unless such objection shall have
been urged before the Secretary or unless there were reasonable grounds for failure so to do.
The finding of the Secretary as to the facts, if supported by substantial evidence, shall be
conclusive. If any person shall apply to the court for leave to adduce additional evidence, and
shall show to the satisfaction of the court that such additional evidence is material and that
there were reasonable grounds for failure to adduce such evidence in the proceeding before
the Secretary, the court may order such additional evidence to be taken before the Secretary
and to be adduced upon the hearing in such manner and upon such terms and conditions as to
the court may seem proper. The Secretary may modify his findings as to the facts by reason of
the additional evidence so taken, and he shall file with the court such modified findings which,
if supported by substantial evidence, shall be conclusive, and his recommendation, if any, for
the setting aside of the original order. The judgment of the court affirming or setting aside any
such order of the Secretary shall be final, subject to review by the Supreme Court of the United
States upon certiorari or certification as provided in section 1254 of title 28 of the United States
Code. The commencement of proceedings under this subsection shall not, unless specifically
ordered by the court to the contrary, operate as a stay of the Secretary’s order.
(i)(1) The Secretary shall promulgate regulations for exempting from the operation of the
foregoing subsections of this section drugs intended solely for investigational use by experts
qualified by scientific training and experience to investigate the safety and effectiveness of
drugs. Such regulations may, within the discretion of the Secretary, among other conditions
relating to the protection of the public health, provide for conditioning such exemption upon—
(A) the submission to the Secretary, before any clinical testing of a new drug is undertaken, of
reports, by the manufacturer or the sponsor of the investigation of such drug, or preclinical
tests (including tests on animals) of such drug adequate to justify the proposed clinical testing;
(B) the manufacturer or the sponsor of the investigation of a new drug proposed to be
distributed to investigators for clinical testing obtaining a signed agreement from each of such
investigators that patients to whom the drug is administered will be under his personal
supervision, or under the supervision of investigators responsible to him, and that he will not
supply such drug to any other investigator, or to clinics, for administration to human beings;
(C) the establishment and maintenance of such records, and the making of such reports to the
Secretary, by the manufacturer or the sponsor of the investigation of such drug, of data
(including but not limited to analytical reports by investigators) obtained as the result of such
investigational use of such drug, as the Secretary finds will enable him to evaluate the safety
and effectiveness of such drug in the event of the filing of an application pursuant to
subsection (b) ; and
(D) 18 the submission to the Secretary by the manufacturer or the sponsor of the investigation
of a new drug of a statement of intent regarding whether the manufacturer or sponsor has
plans for assessing pediatric safety and efficacy.
(2) Subject to paragraph (3), a clinical investigation of a new drug may begin 30 days after the
Secretary has received from the manufacturer or sponsor of the investigation a submission
containing such information about the drug and the clinical investigation, including—
(A) information on design of the investigation and adequate reports of basic information,
certified by the applicant to be accurate reports, necessary to assess the safety of the drug for
use in clinical investigation; and
(B) adequate information on the chemistry and manufacturing of the drug, controls available
for the drug, and primary data tabulations from animal or human studies.
(3)(A) At any time, the Secretary may prohibit the sponsor of an investigation from conducting
the investigation (referred to in this paragraph as a ‘‘clinical hold’’) if the Secretary makes a
determination described in subparagraph (B). The Secretary shall specify the basis for the
clinical hold, including the specific information available to the Secretary which served as the
basis for such clinical hold, and confirm such determination in writing.
(B) For purposes of subparagraph (A), a determination described in this subparagraph with
respect to a clinical hold is that—
(i) the drug involved represents an unreasonable risk to the safety of the persons who are the
subjects of the clinical investigation, taking into account the qualifications of the clinical
investigators, information about the drug, the design of the clinical investigation, the condition
for which the drug is to be investigated, and the health status of the subjects involved; or
(ii) the clinical hold should be issued for such other reasons as the Secretary may by regulation
establish (including reasons established by regulation before the date of the enactment of the
Food and Drug Administration Modernization Act of 1997).
(C) Any written request to the Secretary from the sponsor of an investigation that a clinical hold
be removed shall receive a decision, in writing and specifying the reasons therefor, within 30
days after receipt of such request. Any such request shall include sufficient information to
support the removal of such clinical hold.
(4) Regulations under paragraph (1) shall provide that such exemption shall be conditioned
upon the manufacturer, or the sponsor of the investigation, requiring that experts using such
drugs for investigational purposes certify to such manufacturer or sponsor that they will inform
any human beings to whom such drugs, or any controls used in connection therewith, are
being administered, or their representatives, that such drugs are being used for investigational
purposes and will obtain the consent of such human beings or their representatives, except
where it is not feasible or it is contrary to the best interests of such human beings. Nothing in
this subsection shall be construed to require any clinical investigator to submit directly to the
Secretary reports on the investigational use of drugs.
(j)(1) Any person may file with the Secretary an abbreviated application for the approval of a
new drug.
(2)(A) An abbreviated application for a new drug shall contain—
(i) information to show that the conditions of use prescribed, recommended, or suggested in
the labeling proposed for the new drug have been previously approved for a drug listed under
paragraph (7) (hereinafter in this subsection referred to as a ‘‘listed drug’’);
(ii)(I) if the listed drug referred to in clause (i) has only one active ingredient, information to
show that the active ingredient of the new drug is the same as that of the listed drug;
(II) if the listed drug referred to in clause (i) has more than one active ingredient, information to
show that the active ingredients of the new drug are the same as those of the listed drug, or
(III) if the listed drug referred to in clause (i) has more than one active ingredient and if one of
the active ingredients of the new drug is different and the application is filed pursuant to the
approval of a petition filed under subparagraph (C), information to show that the other active
ingredients of the new drug are the same as the active ingredients of the listed drug,
information to show that the different active ingredient is an active ingredient of a listed drug or
of a drug which does not meet the requirements of section 201(p), and such other information
respecting the different active ingredient with respect to which the petition was filed as the
Secretary may require;
(iii) information to show that the route of administration, the dosage form, and the strength of
the new drug are the same as those of the listed drug referred to in clause (i), or, if the route of
administration, the dosage form, or the strength of the new drug is different and the application
is filed pursuant to the approval of a petition filed under subparagraph (C), such information
respecting the route of administration, dosage form, or strength with respect to which the
petition was filed as the Secretary may require;
(iv) information to show that the new drug is bioequivalent to the listed drug referred to in
clause (i), except that if the application is filed pursuant to the approval of a petition filed under
subparagraph (C), information to show that the active ingredients of the new drug are of the
same pharmacological or therapeutic class as those of the listed drug referred to in clause (i)
and the new drug can be expected to have the same therapeutic effect as the listed drug when
administered to patients for a condition of use referred to in clause (i);
(v) information to show that the labeling proposed for the new drug is the same as the labeling
approved for the listed drug referred to in clause (i) except for changes required because of
differences approved under a petition filed under subparagraph (C) or because the new drug
and the listed drug are produced or distributed by different manufacturers;
(vi) the items specified in clauses (B) through (F) of subsection (b)(1);
(vii) a certification, the opinion of the applicant and to the best of his knowledge, with respect to
each patent which claims the listed drug referred to in clause (i) or which claims a use for such
listed drug for which the applicant is seeking approval under this subsection and for which
information is required to be filed under subsection (b) or (c)—
(I) that such patent information has not been filed,
(II) that such patent has expired,
(III) of the date on which such patent will expire, or
(IV) that such patent is invalid or will not be infringed by the manufacture, , use, or sale of the
new drug for which the application is submitted; and
(viii) if with respect to the listed drug referred to in clause (i) information was filed under
subsection (b) or (c) for a method of use patent which does not claim a use for which the
applicant is seeking approval under this subsection, a statement that the method of use patent
does not claim such a use.
The Secretary may not require that an abbreviated application contain information in addition
to that required by clauses (i) through (viii).
(B) Notice of opinion that patent is invalid or will not be infringed.—
(i) Agreement to give notice.--An applicant that makes a certification described in
subparagraph (A)(vii)(IV) shall include in the application a statement that the applicant will give
notice as required by this subparagraph.
(ii) Timing of notice.--An applicant that makes a certification described in subparagraph
(A)(vii)(IV) shall give notice as required under this subparagraph—
(I) if the certification is in the application, not later than 20 days after the date of the postmark
on the notice with which the Secretary informs the applicant that the application has been filed;
or
(II) if the certification is in an amendment or supplement to the application, at the time at which
the applicant submits the amendment or supplement, regardless of whether the applicant has
already given notice with respect to another such certification contained in the application or in
an amendment or supplement to the application.
(iii) Recipients of notice.--An applicant required under this subparagraph to give notice shall
give notice to--
(I) each owner of the patent that is the subject of the certification (or a representative of the
owner designated to receive such a notice); and
(II) the holder of the approved application under subsection (b) for the drug that is claimed by
the patent or a use of which is claimed by the patent (or a representative of the holder
designated to receive such a notice).
(iv) Contents of notice.--A notice required under this subparagraph shall--
(I) state that an application that contains data from bioavailability or bioequivalence studies
has been submitted under this subsection for the drug with respect to which the certification is
made to obtain approval to engage in the commercial manufacture, use, or sale of the drug
before the expiration of the patent referred to in the certification; and
(II) include a detailed statement of the factual and legal basis of the opinion of the applicant
that the patent is invalid or will not be infringed.
(C) If a person wants to submit an abbreviated application for a new drug which has a different
active ingredient or whose route of administration, dosage form, or strength differ from that of a
listed drug, such person shall submit a petition to the Secretary seeking permission to file such
an application. The Secretary shall approve or disapprove a petition submitted under this
subparagraph within ninety days of the date the petition is submitted. The Secretary shall
approve such a petition unless the Secretary finds—
(i) that investigations must be conducted to show the safety and effectiveness of the drug or of
any of its active ingredients, the route of administration, the dosage form, or strength which
differ from the listed drug; or
(ii) that any drug with a different active ingredient may not be adequately evaluated for
approval as safe and effective on the basis of the information required to be submitted in an
abbreviated application.
(D)(i) An applicant may not amend or supplement an application to seek approval of a drug
referring to a different listed drug from the listed drug identified in the application as submitted
to the Secretary.
(ii) With respect to the drug for which an application is submitted, nothing in this subsection
prohibits an applicant from amending or supplementing the application to seek approval of a
different strength.
(iii) Within 60 days after the date of the enactment of the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003, 19 the Secretary shall issue guidance defining
the term `listed drug' for purposes of this subparagraph.
(3)(A) The Secretary shall issue guidance for the individuals who review applications
submitted under paragraph (1), which shall relate to promptness in conducting the review,
technical excellence, lack of bias and conflict of interest, and knowledge of regulatory and
scientific standards, and which shall apply equally to all individuals who review such
applications.
(B) The Secretary shall meet with a sponsor of an investigation or an applicant for approval for
a drug under this subsection if the sponsor or applicant makes a reasonable written request for
a meeting for the purpose of reaching agreement on the design and size of bioavailability and
bioequivalence studies needed for approval of such application. The sponsor or applicant shall
provide information necessary for discussion and agreement on the design and size of such
studies. Minutes of any such meeting shall be prepared by the Secretary and made available
to the sponsor or applicant.
(C) Any agreement regarding the parameters of design and size of bioavailability and
bioequivalence studies of a drug under this paragraph that is reached between the Secretary
and a sponsor or applicant shall be reduced to writing and made part of the administrative
record by the Secretary. Such agreement shall not be changed after the testing begins,
except—
(i) with the written agreement of the sponsor or applicant; or
(ii) pursuant to a decision, made in accordance with subparagraph (D) by the director of the
reviewing division, that a substantial scientific issue essential to determining the safety or
effectiveness of the drug has been identified after the testing has begun.
(D) A decision under subparagraph (C)(ii) by the director shall be in writing and the Secretary
shall provide to the sponsor or applicant an opportunity for a meeting at which the director and
the sponsor or applicant will be present and at which the director will document the scientific
issue involved.
(E) The written decisions of the reviewing division shall be binding upon, and may not directly
or indirectly be changed by, the field or compliance office personnel unless such field or
compliance office personnel demonstrate to the reviewing division why such decision should
be modified.
(F) No action by the reviewing division may be delayed because of the unavailability of
information from or action by field personnel unless the reviewing division determines that a
delay is necessary to assure the marketing of a safe and effective drug.
(G) For purposes of this paragraph, the reviewing division is the division responsible for the
review of an application for approval of a drug under this subsection (including scientific
matters, chemistry, manufacturing, and controls).
(4) Subject to paragraph (5), the Secretary shall approve an application for a drug unless the
Secretary finds—
(A) the methods used in, or the facilities and controls used for, the manufacture, processing,
and packing of the drug are inadequate to assure and preserve its identity, strength, quality,
and purity;
(B) information submitted with the application is insufficient to show that each of the proposed
conditions of use have been previously approved for the listed drug referred to in the
application;
(C)(i) if the listed drug has only one active ingredient, information submitted with the
application is insufficient to show that the active ingredient is the same as that of the listed
drug;
(ii) if the listed drug has more than one active ingredient, information submitted with the
application is insufficient to show that the active ingredients are the same as the active
ingredients of the listed drug, or
(iii) if the listed drug has more than one active ingredient and if the application is for a drug
which has an active ingredient different from the listed drug, information submitted with the
application is insufficient to show—
(I) that the other active ingredients are the same as the active ingredients of the listed drug, or
(II) that the different active ingredient is an active ingredient of a listed drug or a drug which
does not meet the requirements of section 201(p). or no petition to file an application for the
drug with the different ingredient was approved under paragraph (2)(C);
(D)(i) if the application is for a drug whose route of administration, dosage form, or strength of
the drug is the same as the route of administration, dosage form, or strength of the listed drug
referred to in the application, information submitted in the application is insufficient to show
that the route of administration, dosage form, or strength is the same as that of the listed drug,
or
(ii) if the application is for a drug whose route of administration, dosage form, or strength of the
drug is different from that of the listed drug referred to in the application, no petition to file an
application for the drug with the different route of administration, dosage form, or strength was
approved under paragraph (2)(C);
(E) if the application was filed pursuant to the approval of a petition under paragraph (2)(C),
the application did not contain the information required by the Secretary respecting the active
ingredient, route of administration, dosage form, or strength which is not the same;
(F) information submitted in the application is insufficient to show that the drug is bioequivalent
to the listed drug referred to in the application or, if the application was filed pursuant to a
petition approved under paragraph (2)(C) information submitted in the application is
insufficient to show that the active ingredients of the new drug are of the same
pharmacological or therapeutic class as those of the listed drug referred to in paragraph
(2)(A)(i) and that the new drug can be expected to have the same therapeutic effect as the
listed drug when administered to patients for a condition of use referred to in such paragraph;
(G) information submitted in the application is insufficient to show that the labeling proposed
for the drug is the same as the labeling approved for the listed drug referred to in the
application except for changes required because of differences approved under a petition filed
under paragraph (2)(C) or because the drug and the listed drug are produced or distributed by
different manufacturers;
(H) information submitted in the application or any other information available to the Secretary
shows that (i) the inactive ingredients of the drug are unsafe for use under the conditions
prescribed, recommended, or suggested in the labeling proposed for the drug, or (ii) the
composition of the drug is unsafe under such conditions because of the type or quantity of
inactive ingredients included or the manner in which the inactive ingredients are included;
(I) the approval under subsection (c) of the listed drug referred to in the application under this
subsection has been withdrawn or suspended for grounds described in the first sentence of
subsection (e), the Secretary has published a notice of opportunity for hearing to withdraw
approval of the listed drug under subsection (c) for grounds described in the first sentence of
subsection (e), the approval under this subsection of the listed drug referred to in the
application under this subsection has been withdrawn or suspended under paragraph (6), or
the Secretary has determined that the listed drug has been withdrawn from sale for safety or
effectiveness reasons;
(J) the application does not meet any other requirement of paragraph (2)(A); or
(K) the application contains an untrue statement of material fact.
(5)(A) Within one hundred and eighty days of the initial receipt of an application under
paragraph (2) or within such additional period as may be agreed upon by the Secretary and
the applicant, the Secretary shall approve or disapprove the application.
(B) The approval of an application submitted under paragraph (2) shall be made effective on
the last applicable date determined by applying the following to each certification made under
paragraph (2)(A)(vii):
(i) If the applicant only made a certification described in subclause (I) or (II) of paragraph
(2)(A)(vii) or in both such subclauses, the approval may be made effective immediately.
(ii) If the applicant made a certification described in subclause (III) of paragraph (2)(A)(vii), the
approval may be made effective on the date certified under subclause (III).
(iii) If the applicant made a certification described in subclause (IV) of paragraph (2)(A)(vii), the
approval shall be made effective immediately unless, before the expiration of 45 days after the
date on which the notice described in paragraph (2)(B) is received, an action is brought for
infringement of the patent that is the subject of the certification and for which information was
submitted to the Secretary under subsection (b)(1) or (c)(2) before the date on which the
application (excluding an amendment or supplement to the application), which the Secretary
later determines to be substantially complete, was submitted. If such an action is brought
before the expiration of such days, the approval shall be made effective upon the expiration of
the thirty-month period beginning on the date of the receipt of the notice provided under
paragraph (2)(B)(i) or such shorter or longer period as the court may order because either
party to the action failed to reasonably cooperate in expediting the action, except that—
(I) if before the expiration of such period the district court decides that the patent is invalid or
not infringed (including any substantive determination that there is no cause of action for
patent infringement or invalidity), the approval shall be made effective on--
(aa) the date on which the court enters judgment reflecting the decision; or
(bb) the date of a settlement order or consent decree signed and entered by the court stating
that the patent that is the subject of the certification is invalid or not infringed;
(II) if before the expiration of such period the district court decides that the patent has been
infringed--
(aa) if the judgment of the district court is appealed, the approval shall be made effective on--
(AA) the date on which the court of appeals decides that the patent is invalid or not infringed
(including any substantive determination that there is no cause of action for patent
infringement or invalidity); or
(BB) the date of a settlement order or consent decree signed and entered by the court of
appeals stating that the patent that is the subject of the certification is invalid or not infringed;
or
(bb) if the judgment of the district court is not appealed or is affirmed, the approval shall be
made effective on the date specified by the district court in a court order under section
271(e)(4)(A) of title 35, United States Code;
(III) if before the expiration of such period the court grants a preliminary injunction prohibiting
the applicant from engaging in the commercial manufacture or sale of the drug until the court
decides the issues of patent validity and infringement and if the court decides that such patent
is invalid or not infringed, the approval shall be made effective as provided in subclause (I); or
(IV) if before the expiration of such period the court grants a preliminary injunction prohibiting
the applicant from engaging in the commercial manufacture or sale of the drug until the court
decides the issues of patent validity and infringement and if the court decides that such patent
has been infringed, the approval shall be made effective as provided in subclause (II).
In such an action, each of the parties shall reasonably cooperate in expediting the action.
(iv) 180-day exclusivity period.--
(I) Effectiveness of application.--Subject to subparagraph (D), if the application contains a
certification described in paragraph (2)(A)(vii)(IV) and is for a drug for which a first applicant
has submitted an application containing such a certification, the application shall be made
effective on the date that is 180 days after the date of the first commercial marketing of the
drug (including the commercial marketing of the listed drug) by any first applicant.
(II) Definitions.--In this paragraph:
(aa) 180-day exclusivity period.--The term `180-day exclusivity period' means the 180-day
period ending on the day before the date on which an application submitted by an applicant
other than a first applicant could become effective under this clause.
(bb) First applicant.--As used in this subsection, the term `first applicant' means an applicant
that, on the first day on which a substantially complete application containing a certification
described in paragraph (2)(A)(vii)(IV) is submitted for approval of a drug, submits a
substantially complete application that contains and lawfully maintains a certification described
in paragraph (2)(A)(vii)(IV) for the drug.
(cc) Substantially complete application.--As used in this subsection, the term `substantially
complete application' means an application under this subsection that on its face is sufficiently
complete to permit a substantive review and contains all the information required by paragraph
(2)(A).
(dd) Tentative approval.--
(AA) In general.--The term `tentative approval' means notification to an applicant by the
Secretary that an application under this subsection meets the requirements of paragraph
(2)(A), but cannot receive effective approval because the application does not meet the
requirements of this subparagraph, there is a period of exclusivity for the listed drug under
subparagraph (F) or section 505A, or there is a 7-year period of exclusivity for the listed drug
under section 527.
(BB) Limitation.--A drug that is granted tentative approval by the Secretary is not an approved
drug and shall not have an effective approval until the Secretary issues an approval after any
necessary additional review of the application.
(C) Civil action to obtain patent certainty.--
(i) Declaratory judgment absent infringement action.--
(I) In general.--No action may be brought under section 2201 of title 28, United States Code,
by an applicant under paragraph (2) for a declaratory judgment with respect to a patent which
is the subject of the certification referred to in subparagraph (B)(iii) unless--
(aa) the 45-day period referred to in such subparagraph has expired;
(bb) neither the owner of such patent nor the holder of the approved application under
subsection (b) for the drug that is claimed by the patent or a use of which is claimed by the
patent brought a civil action against the applicant for infringement of the patent before the
expiration of such period; and
(cc) in any case in which the notice provided under paragraph (2)(B) relates to
noninfringement, the notice was accompanied by a document described in subclause (III).
(II) Filing of civil action.--If the conditions described in items (aa), (bb), and as applicable, (cc)
of subclause (I) have been met, the applicant referred to in such subclause may, in
accordance with section 2201 of title 28, United States Code, bring a civil action under such
section against the owner or holder referred to in such subclause (but not against any owner or
holder that has brought such a civil action against the applicant, unless that civil action was
dismissed without prejudice) for a declaratory judgment that the patent is invalid or will not be
infringed by the drug for which the applicant seeks approval, except that such civil action may
be brought for a declaratory judgment that the patent will not be infringed only in a case in
which the condition described in subclause (I)(cc) is applicable. A civil action referred to in this
subclause shall be brought in the judicial district where the defendant has its principal place of
business or a regular and established place of business.
(III) Offer of confidential access to application.--For purposes of subclause (I)(cc), the
document described in this subclause is a document providing an offer of confidential access
to the application that is in the custody of the applicant under paragraph (2) for the purpose of
determining whether an action referred to in subparagraph (B)(iii) should be brought. The
document providing the offer of confidential access shall contain such restrictions as to
persons entitled to access, and on the use and disposition of any information accessed, as
would apply had a protective order been entered for the purpose of protecting trade secrets
and other confidential business information. A request for access to an application under an
offer of confidential access shall be considered acceptance of the offer of confidential access
with the restrictions as to persons entitled to access, and on the use and disposition of any
information accessed, contained in the offer of confidential access, and those restrictions and
other terms of the offer of confidential access shall be considered terms of an enforceable
contract. Any person provided an offer of confidential access shall review the application for
the sole and limited purpose of evaluating possible infringement of the patent that is the
subject of the certification under paragraph (2)(A)(vii)(IV) and for no other purpose, and may
not disclose information of no relevance to any issue of patent infringement to any person
other than a person provided an offer of confidential access. Further, the application may be
redacted by the applicant to remove any information of no relevance to any issue of patent
infringement.
(ii) Counterclaim to infringement action.--
(I) In general.--If an owner of the patent or the holder of the approved application under
subsection (b) for the drug that is claimed by the patent or a use of which is claimed by the
patent brings a patent infringement action against the applicant, the applicant may assert a
counterclaim seeking an order requiring the holder to correct or delete the patent information
submitted by the holder under subsection (b) or (c) on the ground that the patent does not
claim either--
(aa) the drug for which the application was approved; or
(bb) an approved method of using the drug.
(II) No independent cause of action.--Subclause (I) does not authorize the assertion of a claim
described in subclause (I) in any civil action or proceeding other than a counterclaim described
in subclause (I).
(iii) No damages.--An applicant shall not be entitled to damages in a civil action under clause (i)
or a counterclaim under clause (ii).
(D) Forfeiture of 180-day exclusivity period.--
(i) Definition of forfeiture event.--In this subparagraph, the term `forfeiture event', with respect
to an application under this subsection, means the occurrence of any of the following:
(I) Failure to market.--The first applicant fails to market the drug by the later of--
(aa) the earlier of the date that is--
(AA) 75 days after the date on which the approval of the application of the first applicant is
made effective under subparagraph (B)(iii); or
(BB) 30 months after the date of submission of the application of the first applicant; or
(bb) with respect to the first applicant or any other applicant (which other applicant has
received tentative approval), the date that is 75 days after the date as of which, as to each of
the patents with respect to which the first applicant submitted and lawfully maintained a
certification qualifying the first applicant for the 180-day exclusivity period under subparagraph
(B)(iv), at least 1 of the following has occurred:
(AA) In an infringement action brought against that applicant with respect to the patent or in a
declaratory judgment action brought by that applicant with respect to the patent, a court enters
a final decision from which no appeal (other than a petition to the Supreme Court for a writ of
certiorari) has been or can be taken that the patent is invalid or not infringed.
(BB) In an infringement action or a declaratory judgment action described in subitem (AA), a
court signs a settlement order or consent decree that enters a final judgment that includes a
finding that the patent is invalid or not infringed.
(CC) The patent information submitted under subsection (b) or (c) is withdrawn by the holder
of the application approved under subsection (b).
(II) Withdrawal of application.--The first applicant withdraws the application or the Secretary
considers the application to have been withdrawn as a result of a determination by the
Secretary that the application does not meet the requirements for approval under paragraph
(4).
(III) Amendment of certification.--The first applicant amends or withdraws the certification for
all of the patents with respect to which that applicant submitted a certification qualifying the
applicant for the 180-day exclusivity period.
(IV) Failure to obtain tentative approval.--The first applicant fails to obtain tentative approval of
the application within 30 months after the date on which the application is filed, unless the
failure is caused by a change in or a review of the requirements for approval of the application
imposed after the date on which the application is filed.
(V) Agreement with another applicant, the listed drug application holder, or a patent
owner.--The first applicant enters into an agreement with another applicant under this
subsection for the drug, the holder of the application for the listed drug, or an owner of the
patent that is the subject of the certification under paragraph (2)(A)(vii)(IV), the Federal Trade
Commission or the Attorney General files a complaint, and there is a final decision of the
Federal Trade Commission or the court with regard to the complaint from which no appeal
(other than a petition to the Supreme Court for a writ of certiorari) has been or can be taken
that the agreement has violated the antitrust laws (as defined in section 1 of the Clayton Act
(15 U.S.C. 12), except that the term includes section 5 of the Federal Trade Commission Act
(15 U.S.C. 45) to the extent that that section applies to unfair methods of competition).
(VI) Expiration of all patents.--All of the patents as to which the applicant submitted a
certification qualifying it for the 180-day exclusivity period have expired.
(ii) Forfeiture.--The 180-day exclusivity period described in subparagraph (B)(iv) shall be
forfeited by a first applicant if a forfeiture event occurs with respect to that first applicant.
(iii) Subsequent applicant.--If all first applicants forfeit the 180-day exclusivity period under
clause (ii)--
(I) approval of any application containing a certification described in paragraph (2)(A)(vii)(IV)
shall be made effective in accordance with subparagraph (B)(iii); and
(II) no applicant shall be eligible for a 180-day exclusivity period.
( E) If the Secretary decides to disapprove an application, the Secretary shall give the
applicant notice of an opportunity for a hearing before the Secretary on the question of
whether such application is approvable. If the applicant elects to accept the opportunity for
hearing by written request within thirty days after such notice, such hearing shall commence
not more than ninety days after the expiration of such thirty days unless the Secretary and the
applicant otherwise agree. Any such hearing shall thereafter be conducted on an expedited
basis and the Secretary’s order thereon shall be issued within ninety days after the date fixed
by the Secretary for filing final briefs.
( F)(i) If an application (other than an abbreviated new drug application) submitted under
subsection (b) for a drug, no active ingredient (including any ester or salt of the active
ingredient) of which has been approved in any other application under subsection (b), was
approved during the period beginning January 1, 1982, and ending on the date of the
enactment of this subsection 20 , the Secretary may not make the approval of an application
submitted under this subsection which refers to the drug for which the subsection (b)
application was submitted effective before the expiration of ten years from the date of the
approval of the application under subsection (b).
(ii) If an application submitted under subsection (b) for a drug, no active ingredient (including
any ester or salt of the active ingredient) of which has been approved in any other application
under subsection (b), is approved after the date of the enactment of this subsection, no
application may be submitted under this subsection which refers to the drug for which the
subsection (b) application was submitted before the expiration of five years from the date of
the approval of the application under subsection (b), except that such an application may be
submitted under this subsection after the expiration of four years from the date of the approval
of the subsection (b) application if it contains a certification of patent invalidity or
noninfringement described in subclause (IV) of paragraph (2)(A)(vii). The approval of such an
application shall be made effective in accordance with subparagraph (B) except that, if an
action for patent infringement is commenced during the one-year period beginning forty-eight
months after the date of the approval of the subsection (b) application, the thirty-month period
referred to in subparagraph (B)(iii) shall be extended by such amount of time (if any) which is
required for seven and one-half years to have elapsed from the date of approval of the
subsection (b) application.
(iii) If an application submitted under subsection (b) for a drug, which includes an active
ingredient (including any ester or salt of the active ingredient) that has been approved in
another application approved under subsection (b), is approved after the date of enactment of
this subsection 20 and if such application contains reports of new clinical investigations (other
than bioavailability studies) essential to the approval of the application and conducted or
sponsored by the applicant, the Secretary may not make the approval of an application
submitted under this subsection for the conditions of approval of such drug in the subsection (b)
application effective before the expiration of three years from the date of the approval of the
application under subsection (b) for such drug.
(iv) If a supplement to an application approved under subsection (b) is approved after the date
of enactment of this subsection 20 and the supplement contains reports of new clinical
investigations (other than bioavailability studies) essential to the approval of the supplement
and conducted or sponsored by the person submitting the supplement, the Secretary may not
make the approval of an application submitted under this subsection for a change approved in
the supplement effective before the expiration of three years from the date of the approval of
the supplement under subsection (b).
(v) If an application (or supplement to an application) submitted under subsection (b) for a drug,
which includes an active ingredient (including any ester or salt of the active ingredient) that has
been approved in another application under subsection (b), was approved during the period
beginning January 1, 1982, and ending on the date of the enactment of this subsection 21 , the
Secretary may not make the approval of an application submitted under this subsection which
refers to the drug for which the subsection (b) application was submitted or which refers to a
change approved in a supplement to the subsection (b) application effective before the
expiration of two years from the date of enactment of this subsection 21.
(6) If a drug approved under this subsection refers in its approved application to a drug the
approval of which was withdrawn or suspended for grounds described in the first sentence of
subsection (e) or was withdrawn or suspended under this paragraph or which, as determined
by the Secretary, has been withdrawn from sale for safety or effectiveness reasons, the
approval of the drug under this subsection shall be withdrawn or suspended—
(A) for the same period as the withdrawal or suspension under subsection (e) or this
paragraph, or
(B) if the listed drug has been withdrawn from sale, for the period of withdrawal from sale or, if
earlier, the period ending on the date the Secretary determines that the withdrawal from sale is
not for safety or effectiveness reasons.
(7)(A)(i) Within sixty days of the date of the enactment of this subsection 22 , the Secretary
shall publish and make available to the public—
(I) a list in alphabetical order of the official and proprietary name of each drug which has been
approved for safety and effectiveness under subsection (c) before the date of the enactment of
this subsection 21;
(II) the date of approval if the drug is approved after 1981 and the number of the application
which was approved; and
(III) whether in vitro or in vivo bioequivalence studies, or both such studies, are required for
applications filed under this subsection which will refer to the drug published.
(ii) Every thirty days after the publication of the first list under clause (i) the Secretary shall
revise the list to include each drug which has been approved for safety and effectiveness
under subsection (c) or approved under this subsection during the thirty day period.
(iii) When patent information submitted under subsection (b) or (c) respecting a drug included
on the list is to be published by the Secretary, the Secretary shall, in revisions made under
clause (ii), include such information for such drug.
(B) A drug approved for safety and effectiveness under subsection (c) or approved under this
subsection shall, for purposes of this subsection, be considered to have been published under
subparagraph (A) on the date of its approval or the date of enactment 23 , whichever is later.
(C) If the approval of a drug was withdrawn or suspended for grounds described in the first
sentence of subsection (e) or was withdrawn or suspended under paragraph (6) or if the
Secretary determines that a drug has been withdrawn from sale for safety or effectiveness
reasons, it may not be published in the list under subparagraph (A) or, if the withdrawal or
suspension occurred after its publication in such list, it shall be immediately removed from
such list—
(i) for the same period as the withdrawal or suspension under subsection (e) or paragraph (6),
or
(ii) if the listed drug has been withdrawn from sale, for the period of withdrawal from sale or, if
earlier, the period ending on the date the Secretary determines that the withdrawal from sale is
not for safety or effectiveness reasons.
A notice of the removal shall be published in the Federal Register.
(8) 24 For purposes of this subsection:
(A)(i) The term `bioavailability' means the rate and extent to which the active ingredient or
therapeutic ingredient is absorbed from a drug and becomes available at the site of drug
action.
(ii) For a drug that is not intended to be absorbed into the bloodstream, the Secretary may
assess bioavailability by scientifically valid measurements intended to reflect the rate and
extent to which the active ingredient or therapeutic ingredient becomes available at the site of
drug action.
(B) A drug shall be considered to be bioequivalent to a listed drug if—
(i) the rate and extent of absorption of the drug do not show a significant difference from the
rate and extent of absorption of the listed drug when administered at the same molar dose of
the therapeutic ingredient under similar experimental conditions in either a single dose or
multiple doses; or
(ii) the extent of absorption of the drug does not show a significant difference from the extent of
absorption of the listed drug when administered at the same molar dose of the therapeutic
ingredient under similar experimental conditions in either a single dose or multiple doses and
the difference from the listed drug in the rate of absorption of the drug is intentional, is reflected
in its proposed labeling, is not essential to the attainment of effective body drug concentrations
on chronic use, and is considered medically insignificant for the drug.
(C) For a drug that is not intended to be absorbed into the bloodstream, the Secretary may
establish alternative, scientifically valid methods to show bioequivalence if the alternative
methods are expected to detect a significant difference between the drug and the listed drug in
safety and therapeutic effect.
(9) The Secretary shall, with respect to each application submitted under this subsection,
maintain a record of—
(A) the name of the applicant,
(B) the name of the drug covered by the application,
(C) the name of each person to whom the review of the chemistry of the application was
assigned and the date of such assignment, and
(D) the name of each person to whom the bioequivalence review for such application was
assigned and the date of such assignment.
The information the Secretary is required to maintain under this paragraph with respect to an
application submitted under this subsection shall be made available to the public after the
approval of such application.
(k)(1) In the case of any drug for which an approval of an application filed under subsection (b)
or (j) is in effect, the applicant shall establish and maintain such records, and make such
reports to the Secretary, of data relating to clinical experience and other data or information,
received or otherwise obtained by such applicant with respect to such drug, as the Secretary
may by general regulation, or by order with respect to such application, prescribe on the basis
of a finding that such records and reports are necessary in order to enable the Secretary to
determine, or facilitate a determination, whether there is or may be ground for invoking
subsection (e) of this section. Regulations and orders issued under this subsection and under
subsection (i) shall have due regard for the professional ethics of the medical profession and
the interests of patients and shall provide, where the Secretary deems it to be appropriate, for
the examination, upon request, by the persons to whom such regulations or orders are
applicable, of similar information received or otherwise obtained by the Secretary.
(2) Every person required under this section to maintain records, and every person in charge
or custody thereof, shall, upon request of an officer or employee designated by the Secretary,
permit such officer or employee at all reasonable times to have access to and copy and verify
such records.
(l) Safety and effectiveness data and information which has been submitted in an application
under subsection (b) for a drug and which has not previously been disclosed to the public shall
be made available to the public, upon request, unless extraordinary circumstances are
shown—
(1) if no work is being or will be undertaken to have the application approved,
(2) if the Secretary has determined that the application is not approvable and all legal appeals
have been exhausted,
(3) if approval of the application under subsection (c) is withdrawn and all legal appeals have
been exhausted,
(4) if the Secretary has determined that such drug is not a new drug, or
(5) upon the effective date of the approval of the first application under subsection (j) which
refers to such drug or upon the date upon which the approval of an application under
subsection (j) which refers to such drug could be made effective if such an application had
been submitted.
(m) For purposes of this section, the term ‘‘patent’’ means a patent issued by the United States
Patent and Trademark Office.
(n)(1) For the purpose of providing expert scientific advice and recommendations to the
Secretary regarding a clinical investigation of a drug or the approval for marketing of a drug
under section 505 or section 351 of the Public Health Service Act, the Secretary shall establish
panels of experts or use panels of experts established before the date of enactment of the
Food and Drug Administration Modernization Act of 1997, or both.
(2) The Secretary may delegate the appointment and oversight authority granted under section
904 to a director of a center or successor entity within the Food and Drug Administration.
(3) The Secretary shall make appointments to each panel established under paragraph (1) so
that each panel shall consist of—
(A) members who are qualified by training and experience to evaluate the safety and
effectiveness of the drugs to be referred to the panel and who, to the extent feasible, possess
skill and experience in the development, manufacture, or utilization of such drugs;
(B) members with diverse expertise in such fields as clinical and administrative medicine,
pharmacy, pharmacology, pharmacoeconomics, biological and physical sciences, and other
related professions;
(C) a representative of consumer interests, and a representative of interests of the drug
manufacturing industry not directly affected by the matter to be brought before the panel; and
(D) two or more members who are specialists or have other expertise in the particular disease
or condition for which the drug under review is proposed to be indicated.
Scientific, trade, and consumer organizations shall be afforded an opportunity to nominate
individuals for appointment to the panels. No individual who is in the regular full-time employ of
the United States and engaged in the administration of this Act may be a voting member of any
panel. The Secretary shall designate one of the members of each panel to serve as chairman
thereof.
(4) Each member of a panel shall publicly disclose all conflicts of interest that member may
have with the work to be undertaken by the panel. No member of a panel may vote on any
matter where the member or the immediate family of such member could gain financially from
the advice given to the Secretary. The Secretary may grant a waiver of any conflict of interest
requirement upon public disclosure of such conflict of interest if such waiver is necessary to
afford the panel essential expertise, except that the Secretary may not grant a waiver for a
member of a panel when the member’s own scientific work is involved.
(5) The Secretary shall, as appropriate, provide education and training to each new panel
member before such member participates in a panel’s activities, including education regarding
requirements under this Act and related regulations of the Secretary, and the administrative
processes and procedures related to panel meetings.
(6) Panel members (other than officers or employees of the United States), while attending
meetings or conferences of a panel or otherwise engaged in its business, shall be entitled to
receive compensation for each day so engaged, including traveltime, at rates to be fixed by the
Secretary, but not to exceed the daily equivalent of the rate in effect for positions classified
above grade GS–15 of the General Schedule. While serving away from their homes or regular
places of business, panel members may be allowed travel expenses (including per diem in lieu
of subsistence) as authorized by section 5703 of title 5, United States Code, for persons in the
Government service employed intermittently.
(7) The Secretary shall ensure that scientific advisory panels meet regularly and at appropriate
intervals so that any matter to be reviewed by such a panel can be presented to the panel not
more than 60 days after the matter is ready for such review. Meetings of the panel may be held
using electronic communication to convene the meetings.
(8) Within 90 days after a scientific advisory panel makes recommendations on any matter
under its review, the Food and Drug Administration official responsible for the matter shall
review the conclusions and recommendations of the panel, and notify the affected persons of
the final decision on the matter, or of the reasons that no such decision has been reached.
Each such final decision shall be documented including the rationale for the decision.
SEC. 505A. [ 21 U.S.C. 355a] PEDIATRIC STUDIES OF DRUGS. 25
( a) DEFINITIONS.—As used in this section, the term ‘‘pediatric studies’’ or ‘‘studies’’ means at
least one clinical investigation (that, at the Secretary’s discretion, may include pharmacokinetic
studies) in pediatric age groups (including neonates in appropriate cases) in which a drug is
anticipated to be used.
( b) MARKET EXCLUSIVITY FOR NEW DRUGS.—If, prior to approval of an application that is
submitted under section 505(b)(1), the Secretary determines that information relating to the
use of a new drug in the pediatric population may produce health benefits in that population,
the Secretary makes a written request for pediatric studies (which shall include a timeframe for
completing such studies), and such studies are completed within any such timeframe and the
reports thereof submitted in accordance with subsection (d)(2) or accepted in accordance with
subsection (d)(3)—
(1)(A)(i) the period referred to in subsection (c)(3)(D)(ii) of section 505, and in subsection
(j)(5)(F)(ii)of such section, is deemed to be five years and six months rather than five years,
and the references in subsections (c)(3)(D)(ii) and (j)(5)(F)(ii) of such section to four years, to
forty-eight months, and to seven and one-half years are deemed to be four and one-half years,
fifty-four months, and eight years, respectively; or
(ii) the period referred to in clauses (iii) and (iv) of subsection (c)(3)(D) of such section, and in
clauses (iii) and (iv) of subsection (j)(5)(F) of such section, is deemed to be three years and six
months rather than three years; and
(B) if the drug is designated under section 526 for a rare disease or condition, the period
referred to in section 527(a) is deemed to be seven years and six months rather than seven
years; and
(2)(A) if the drug is the subject of—
(i) a listed patent for which a certification has been submitted under subsection (b)(2)(A)(ii) or
(j)(2)(A)(vii)(II) of section 505 and for which pediatric studies were submitted prior to the
expiration of the patent (including any patent extensions); or
(ii) a listed patent for which a certification has been submitted under subsections (b)(2)(A)(iii)
or (j)(2)(A)(vii)(III) of section 505,
the period during which an application may not be approved under section 505(c)(3) or section
505(j)(5)(B) shall be extended by a period of six months after the date the patent expires
(including any patent extensions); or
(B) if the drug is the subject of a listed patent for which a certification has been submitted
under subsection (b)(2)(A)(iv) or (j)(2)(A)(vii)(IV) of section 505, and in the patent infringement
litigation resulting from the certification the court determines that the patent is valid and would
be infringed, the period during which an application may not be approved under section
505(c)(3) or section 505(j)(5)(B) shall be extended by a period of six months after the date the
patent expires (including any patent extensions).
(c) MARKET EXCLUSIVITY FOR ALREADY-MARKETED DRUGS.—If the Secretary
determines that information relating to the use of an approved drug in the pediatric population
may produce health benefits in that population and makes a written request to the holder of an
approved application under section 505(b)(1) for pediatric studies (which shall include a
timeframe for completing such studies) , the holder agrees to the request, the studies are
completed within any such timeframe, and the reports thereof are submitted in accordance
with subsection (d)(2) or accepted in accordance with subsection (d)(3)—
(1)(A)(i) the period referred to in subsection (c)(3)(D)(ii) of section 505, and in subsection
(j)(5)(F)(ii) of such section, is deemed to be five years and six months rather than five years,
and the references in subsections (c)(3)(D)(ii) and (j)(5)(F)(ii) of such section to four years, to
forty-eight months, and to seven and one-half years are deemed to be four and one-half years,
fifty-four months, and eight years, respectively; or
(ii) the period referred to in clauses (iii) and (iv) of subsection (c)(3)(D) of such section, and in
clauses (iii) and (iv) of subsection (j)(5)(F) of such section, is deemed to be three years and six
months rather than three years; and
(B) if the drug is designated under section 526 for a rare disease or condition, the period
referred to in section 527(a) is deemed to be seven years and six months rather than seven
years; and
(2)(A) if the drug is the subject of—
(i) a listed patent for which a certification has been submitted under subsection (b)(2)(A)(ii) or
(j)(2)(A)(vii)(II) of section 505 and for which pediatric studies were submitted prior to the
expiration of the patent (including any patent extensions); or
(ii) a listed patent for which a certification has been submitted under subsection (b)(2)(A)(iii) or
(j)(2)(A)(vii)(III) of section 505,
the period during which an application may not be approved under section 505(c)(3) or section
505(j)(5)(B)(ii) shall be extended by a period of six months after the date the patent expires
(including any patent extensions); or
(B) if the drug is the subject of a listed patent for which a certification has been submitted
under subsection (b)(2)(A)(iv) or (j)(2)(A)(vii)(IV) of section 505, and in the patent infringement
litigation resulting from the certification the court determines that the patent is valid and would
be infringed, the period during which an application may not be approved under section
505(c)(3) or section 505(j)(5)(B) shall be extended by a period of six months after the date the
patent expires (including any patent extensions).
(d) CONDUCT OF PEDIATRIC STUDIES.—
(1) AGREEMENT FOR STUDIES.—The Secretary may, pursuant to a written request from the
Secretary under subsection (b) or (c), after consultation with—
(A) the sponsor of an application for an investigational new drug under section 505(i);
(B) the sponsor of an application for a new drug under section 505(b)(1); or
(C) the holder of an approved application for a drug under section 505(b)(1),
agree with the sponsor or holder for the conduct of pediatric studies for such drug. Such
agreement shall be in writing and shall include a timeframe for such studies.
(2) WRITTEN PROTOCOLS TO MEET THE STUDIES REQUIREMENT.— If the sponsor or
holder and the Secretary agree upon written protocols for the studies, the studies requirement
of subsection (b) or (c) is satisfied upon the completion of the studies and submission of the
reports thereof in accordance with the original written request and the written agreement
referred to in paragraph (1). In reaching an agreement regarding written protocols, the
Secretary shall take into account adequate representation of children of ethnic and racial
minorities. Not later than 60 days after the submission of the report of the studies, the
Secretary shall determine if such studies were or were not conducted in accordance with the
original written request and the written agreement and reported in accordance with the
requirements of the Secretary for filing and so notify the sponsor or holder.
(3) OTHER METHODS TO MEET THE STUDIES REQUIREMENT.— If the sponsor or holder
and the Secretary have not agreed in writing on the protocols for the studies, the studies
requirement of subsection (b) or (c) is satisfied when such studies have been completed and
the reports accepted by the Secretary. Not later than 90 days after the submission of the
reports of the studies, the Secretary shall accept or reject such reports and so notify the
sponsor or holder. The Secretary’s only responsibility in accepting or rejecting the reports shall
be to determine, within the 90 days, whether the studies fairly respond to the written request,
have been conducted in accordance with commonly accepted scientific principles and
protocols, and have been reported in accordance with the requirements of the Secretary for
filing.
(4) WRITTEN REQUEST TO HOLDERS OF APPROVED APPLICATIONS FOR DRUGS
THAT HAVE MARKET EXCLUSIVITY-
(A) REQUEST AND RESPONSE- If the Secretary makes a written request for pediatric
studies (including neonates, as appropriate) under subsection (c) to the holder of an
application approved under section 505(b)(1), the holder, not later than 180 days after
receiving the written request, shall respond to the Secretary as to the intention of the holder to
act on the request by--
(i) indicating when the pediatric studies will be initiated, if the holder agrees to the request; or
(ii) indicating that the holder does not agree to the request.
(B) NO AGREEMENT TO REQUEST-
(i) REFERRAL- If the holder does not agree to a written request within the time period
specified in subparagraph (A), and if the Secretary determines that there is a continuing need
for information relating to the use of the drug in the pediatric population (including neonates, as
appropriate), the Secretary shall refer the drug to the Foundation for the National Institutes of
Health established under section 499 of the Public Health Service Act (42 U.S.C. 290b)
(referred to in this paragraph as the `Foundation') for the conduct of the pediatric studies
described in the written request.
(ii) PUBLIC NOTICE- The Secretary shall give public notice of the name of the drug, the name
of the manufacturer, and the indications to be studied made in a referral under clause (i).
(C) LACK OF FUNDS- On referral of a drug under subparagraph (B)(i), the Foundation shall
issue a proposal to award a grant to conduct the requested studies unless the Foundation
certifies to the Secretary, within a timeframe that the Secretary determines is appropriate
through guidance, that the Foundation does not have funds available under section
499(j)(9)(B)(i) 26 to conduct the requested studies. If the Foundation so certifies, the Secretary
shall refer the drug for inclusion on the list established under section 409I of the Public Health
Service Act for the conduct of the studies.
(D) EFFECT OF SUBSECTION- Nothing in this subsection (including with respect to referrals
from the Secretary to the Foundation) alters or amends section 301(j) of this Act or section 552
of title 5 or section 1905 of title 18, United States Code.
(E) NO REQUIREMENT TO REFER- Nothing in this subsection shall be construed to require
that every declined written request shall be referred to the Foundation.
(F) WRITTEN REQUESTS UNDER SUBSECTION (b)- For drugs under subsection (b) for
which written requests have not been accepted, if the Secretary determines that there is a
continuing need for information relating to the use of the drug in the pediatric population
(including neonates, as appropriate), the Secretary shall issue a written request under
subsection (c) after the date of approval of the drug.
(e) DELAY OF EFFECTIVE DATE FOR CERTAIN APPLICATION.—If the Secretary
determines that the acceptance or approval of an application under section 505(b)(2) or 505(j)
for a new drug may occur after submission of reports of pediatric studies under this section,
which were submitted prior to the expiration of the patent (including any patent extension) or
the applicable period under clauses (ii) through (iv) of section 505(c)(3)(D) or clauses (ii)
through (iv) of section 505(j)(5)(F), but before the Secretary has determined whether the
requirements of subsection (d) have been satisfied, the Secretary shall delay the acceptance
or approval under section 505(b)(2) or 505(j) until the determination under subsection (d) is
made, but any such delay shall not exceed 90 days. In the event that requirements of this
section are satisfied, the applicable six month period under subsection ( b) or (c) shall be
deemed to have been running during the period of delay.
(f) NOTICE OF DETERMINATIONS ON STUDIES REQUIREMENT.— The Secretary shall
publish a notice of any determination that the requirements of subsection (d) have been met
and that submissions and approvals under subsection (b)(2) or (j) of section 505 for a drug will
be subject to the provisions of this section.
( g) LIMITATIONS.—A drug to which the six-month period under subsection (b) or (c) has
already been applied—
(1) may receive an additional six-month period under subsection (c)(1)(A)(ii) for a
supplemental application if all other requirements under this section are satisfied, except that
such a drug may not receive any additional such period under subsection (c)(2); and
(2) may not receive any additional such period under subsection (c)(1)(B).
( h) RELATIONSHIP TO PEDIATRIC RESEARCH REQUIREMENTS.—Notwithstanding any
other provision of law, if any pediatric study is required by a provision of law (including a
regulation) other than this section and such study meets the completeness, timeliness, and
other requirements of this section, such study shall be deemed to satisfy the requirement for
market exclusivity pursuant to this section.
(i) LABELING SUPPLEMENTS-
(1) PRIORITY STATUS FOR PEDIATRIC SUPPLEMENTS- Any supplement to an application
under section 505 proposing a labeling change pursuant to a report on a pediatric study under
this section--
(A) shall be considered to be a priority supplement; and
(B) shall be subject to the performance goals established by the Commissioner for priority
drugs.
(2) DISPUTE RESOLUTION-
(A) REQUEST FOR LABELING CHANGE AND FAILURE TO AGREE- If the Commissioner
determines that an application with respect to which a pediatric study is conducted under this
section is approvable and that the only open issue for final action on the application is the
reaching of an agreement between the sponsor of the application and the Commissioner on
appropriate changes to the labeling for the drug that is the subject of the application, not later
than 180 days after the date of submission of the application--
(i) the Commissioner shall request that the sponsor of the application make any labeling
change that the Commissioner determines to be appropriate; and
(ii) if the sponsor of the application does not agree to make a labeling change requested by the
Commissioner, the Commissioner shall refer the matter to the Pediatric Advisory Committee.
(B) ACTION BY THE PEDIATRIC ADVISORY SUBCOMMITTEE OF THE ANTI-INFECTIVE
DRUGS ADVISORY COMMITTEE- Not later than 90 days after receiving a referral under
subparagraph (A)(ii), the Pediatric Advisory Committee shall--
(i) review the pediatric study reports; and
(ii) make a recommendation to the Commissioner concerning appropriate labeling changes, if
any.
(C) CONSIDERATION OF RECOMMENDATIONS- The Commissioner shall consider the
recommendations of the Pediatric Advisory Committee and, if appropriate, not later than 30
days after receiving the recommendation, make a request to the sponsor of the application to
make any labeling change that the Commissioner determines to be appropriate.
(D) MISBRANDING- If the sponsor of the application, within 30 days after receiving a request
under subparagraph (C), does not agree to make a labeling change requested by the
Commissioner, the Commissioner may deem the drug that is the subject of the application to
be misbranded.
(E) NO EFFECT ON AUTHORITY- Nothing in this subsection limits the authority of the United
States to bring an enforcement action under this Act when a drug lacks appropriate pediatric
labeling. Neither course of action (the Pediatric Advisory Committee process or an
enforcement action referred to in the preceding sentence) shall preclude, delay, or serve as
the basis to stay the other course of action.
(j) DISSEMINATION OF PEDIATRIC INFORMATION-
(1) IN GENERAL- Not later than 180 days after the date of submission of a report on a
pediatric study under this section, the Commissioner shall make available to the public a
summary of the medical and clinical pharmacology reviews of pediatric studies conducted for
the supplement, including by publication in the Federal Register.
(2) EFFECT OF SUBSECTION- Nothing in this subsection alters or amends section 301(j) of
this Act or section 552 of title 5 or section 1905 of title 18, United States Code.'.
(k) CLARIFICATION OF INTERACTION OF MARKET EXCLUSIVITY UNDER THIS
SECTION AND MARKET EXCLUSIVITY AWARDED TO AN APPLICANT FOR APPROVAL
OF A DRUG UNDER SECTION 505(j)- If a 180-day period under section 505(j)(5)(B)(iv)
overlaps with a 6-month exclusivity period under this section, so that the applicant for approval
of a drug under section 505(j) entitled to the 180-day period under that section loses a portion
of the 180-day period to which the applicant is entitled for the drug, the 180-day period shall be
extended from--
(1) the date on which the 180-day period would have expired by the number of days of the
overlap, if the 180-day period would, but for the application of this subsection, expire after the
6-month exclusivity period; or
(2) the date on which the 6-month exclusivity period expires, by the number of days of the
overlap if the 180-day period would, but for the application of this subsection, expire during the
six-month exclusivity period.
(l) PROMPT APPROVAL OF DRUGS UNDER SECTION 505(j) WHEN PEDIATRIC
INFORMATION IS ADDED TO LABELING-
(1) GENERAL RULE- A drug for which an application has been submitted or approved under
section 505(j) shall not be considered ineligible for approval under that section or misbranded
under section 502 on the basis that the labeling of the drug omits a pediatric indication or any
other aspect of labeling pertaining to pediatric use when the omitted indication or other aspect
is protected by patent or by exclusivity under clause (iii) or (iv) of section 505(j)(5)(F).
(2) LABELING- Notwithstanding clauses (iii) and (iv) of section 505(j)(5)(F), the Secretary may
require that the labeling of a drug approved under section 505(j) that omits a pediatric
indication or other aspect of labeling as described in paragraph (1) include--
(A) a statement that, because of marketing exclusivity for a manufacturer--
(i) the drug is not labeled for pediatric use; or
(ii) in the case of a drug for which there is an additional pediatric use not referred to in
paragraph (1), the drug is not labeled for the pediatric use under paragraph (1); and
(B) a statement of any appropriate pediatric contraindications, warnings, or precautions that
the Secretary considers necessary.
(3) PRESERVATION OF PEDIATRIC EXCLUSIVITY AND OTHER PROVISIONS- This
subsection does not affect--
(A) the availability or scope of exclusivity under this section;
(B) the availability or scope of exclusivity under section 505 for pediatric formulations;
(C) the question of the eligibility for approval of any application under section 505(j) that omits
any other conditions of approval entitled to exclusivity under clause (iii) or (iv) of section
505(j)(5)(F); or
(D) except as expressly provided in paragraphs (1) and (2), the operation of section 505.
(m) REPORT.—The Secretary shall conduct a study and report to Congress not later than
January 1, 2001, based on the experience under the program established under this section.
The study and report shall examine all relevant issues, including—
(1) the effectiveness of the program in improving information about important pediatric uses for
approved drugs;
(2) the adequacy of the incentive provided under this section;
(3) the economic impact of the program on taxpayers and consumers, including the impact of
the lack of lower cost generic drugs on patients, including on lower income patients; and
(4) any suggestions for modification that the Secretary determines to be appropriate.
(n) SUNSET- A drug may not receive any 6-month period under subsection (b) or (c) 27
unless--
(1) on or before October 1, 2007 , the Secretary makes a written request for pediatric studies
of the drug;
(2) on or before October 1, 2007 , an application for the drug is accepted for filing under
section 505(b); and
(3) all requirements of this section are met.
SEC. 505B. 28 [21 U.S.C. 355c] RESEARCH INTO PEDIATRIC USES FOR DRUGS AND
BIOLOGICAL PRODUCTS.
(a) NEW DRUGS AND BIOLOGICAL PRODUCTS-
(1) IN GENERAL- A person that submits an application (or supplement to an application)—
(A) under section 505 for a new active ingredient, new indication, new dosage form, new
dosing regimen, or new route of administration; or
(B) under section 351 of the Public Health Service Act (42 U.S.C. 262) for a new active
ingredient, new indication, new dosage form, new dosing regimen, or new route of
administration; shall submit with the application the assessments described in paragraph (2).
(2) ASSESSMENTS-
(A) IN GENERAL- The assessments referred to in paragraph (1) shall contain data, gathered
using appropriate formulations for each age group for which the assessment is required, that
are adequate—
(i) to assess the safety and effectiveness of the drug or the biological product for the claimed
indications in all relevant pediatric subpopulations; and
(ii) to support dosing and administration for each pediatric subpopulation for which the drug or
the biological product is safe and effective.
(B) SIMILAR COURSE OF DISEASE OR SIMILAR EFFECT OF DRUG OR BIOLOGICAL
PRODUCT-
(i) IN GENERAL- If the course of the disease and the effects of the drug are sufficiently similar
in adults and pediatric patients, the Secretary may conclude that pediatric effectiveness can be
extrapolated from adequate and well-controlled studies in adults, usually supplemented with
other information obtained in pediatric patients, such as pharmacokinetic studies.
(ii) EXTRAPOLATION BETWEEN AGE GROUPS- A study may not be needed in each
pediatric age group if data from 1 age group can be extrapolated to another age group.
(3) DEFERRAL- On the initiative of the Secretary or at the request of the applicant, the
Secretary may defer submission of some or all assessments required under paragraph (1)
until a specified date after approval of the drug or issuance of the license for a biological
product if--
(A) the Secretary finds that--
(i) the drug or biological product is ready for approval for use in adults before pediatric studies
are complete;
(ii) pediatric studies should be delayed until additional safety or effectiveness data have been
collected; or
(iii) there is another appropriate reason for deferral; and
(B) the applicant submits to the Secretary—
(i) certification of the grounds for deferring the assessments;
(ii) a description of the planned or ongoing studies; and
(iii) evidence that the studies are being conducted or will be conducted with due diligence and
at the earliest possible time.
(4) WAIVERS-
(A) FULL WAIVER- On the initiative of the Secretary or at the request of an applicant, the
Secretary shall grant a full waiver, as appropriate, of the requirement to submit assessments
for a drug or biological product under this subsection if the applicant certifies and the Secretary
finds that--
(i) necessary studies are impossible or highly impracticable (because, for example, the
number of patients is so small or the patients are geographically dispersed);
(ii) there is evidence strongly suggesting that the drug or biological product would be
ineffective or unsafe in all pediatric age groups; or
(iii) the drug or biological product—
(I) does not represent a meaningful therapeutic benefit over existing therapies for pediatric
patients; and
(II) is not likely to be used in a substantial number of pediatric patients.
(B) PARTIAL WAIVER- On the initiative of the Secretary or at the request of an applicant, the
Secretary shall grant a partial waiver, as appropriate, of the requirement to submit
assessments for a drug or biological product under this subsection with respect to a specific
pediatric age group if the applicant certifies and the Secretary finds that—
(i) necessary studies are impossible or highly impracticable (because, for example, the
number of patients in that age group is so small or patients in that age group are
geographically dispersed);
(ii) there is evidence strongly suggesting that the drug or biological product would be
ineffective or unsafe in that age group;
(iii) the drug or biological product—
(I) does not represent a meaningful therapeutic benefit over existing therapies for pediatric
patients in that age group; and
(II) is not likely to be used by a substantial number of pediatric patients in that age group; or
(iv) the applicant can demonstrate that reasonable attempts to produce a pediatric formulation
necessary for that age group have failed
(C) PEDIATRIC FORMULATION NOT POSSIBLE- If a waiver is granted on the ground that it
is not possible to develop a pediatric formulation, the waiver shall cover only the pediatric
groups requiring that formulation.
(D) LABELING REQUIREMENT- If the Secretary grants a full or partial waiver because there
is evidence that a drug or biological product would be ineffective or unsafe in pediatric
populations, the information shall be included in the labeling for the drug or biological product.
(b) MARKETED DRUGS AND BIOLOGICAL PRODUCTS-
(1) IN GENERAL- After providing notice in the form of a letter and an opportunity for written
response and a meeting, which may include an advisory committee meeting, the Secretary
may (by order in the form of a letter) require the holder of an approved application for a drug
under section 505 or the holder of a license for a biological product under section 351 of the
Public Health Service Act (42 U.S.C. 262) to submit by a specified date the assessments
described in subsection (a)(2) if the Secretary finds that—
(A)(i) the drug or biological product is used for a substantial number of pediatric patients for the
labeled indications; and
(ii) the absence of adequate labeling could pose significant risks to pediatric patients; or
(B)(i) there is reason to believe that the drug or biological product would represent a
meaningful therapeutic benefit over existing therapies for pediatric patients for 1 or more of the
claimed indications; and
(ii) the absence of adequate labeling could pose significant risks to pediatric patients.
(2) WAIVERS-
(A) FULL WAIVER- At the request of an applicant, the Secretary shall grant a full waiver, as
appropriate, of the requirement to submit assessments under this subsection if the applicant
certifies and the Secretary finds that--
(i) necessary studies are impossible or highly impracticable (because, for example, the
number of patients in that age group is so small or patients in that age group are
geographically dispersed); or
(ii) there is evidence strongly suggesting that the drug or biological product would be
ineffective or unsafe in all pediatric age groups.
(B) PARTIAL WAIVER- At the request of an applicant, the Secretary shall grant a partial
waiver, as appropriate, of the requirement to submit assessments under this subsection with
respect to a specific pediatric age group if the applicant certifies and the Secretary finds that--
(i) necessary studies are impossible or highly impracticable (because, for example, the
number of patients in that age group is so small or patients in that age group are
geographically dispersed);
(ii) there is evidence strongly suggesting that the drug or biological product would be
ineffective or unsafe in that age group;
(iii)(I) the drug or biological product--
(aa) does not represent a meaningful therapeutic benefit over existing therapies for pediatric
patients in that age group; and
(bb) is not likely to be used in a substantial number of pediatric patients in that age group; and
(II) the absence of adequate labeling could not pose significant risks to pediatric patients; or
(iv) the applicant can demonstrate that reasonable attempts to produce a pediatric formulation
necessary for that age group have failed.
(C) PEDIATRIC FORMULATION NOT POSSIBLE- If a waiver is granted on the ground that it
is not possible to develop a pediatric formulation, the waiver shall cover only the pediatric
groups requiring that formulation.
(D) LABELING REQUIREMENT- If the Secretary grants a full or partial waiver because there
is evidence that a drug or biological product would be ineffective or unsafe in pediatric
populations, the information shall be included in the labeling for the drug or biological product.
(3) RELATIONSHIP TO OTHER PEDIATRIC PROVISIONS-
(A) NO ASSESSMENT WITHOUT WRITTEN REQUEST- No assessment may be required
under paragraph (1) for a drug subject to an approved application under section 505 unless--
(i) the Secretary has issued a written request for a related pediatric study under section 505A(c)
of this Act or section 409I of the Public Health Service Act (42 U.S.C. 284m);
(ii)(I) if the request was made under section 505A(c)--
(aa) the recipient of the written request does not agree to the request; or
(bb) the Secretary does not receive a response as specified under section 505A(d)(4)(A); or
(II) if the request was made under section 409I of the Public Health Service Act (42 U.S.C.
284m)--
(aa) the recipient of the written request does not agree to the request; or
(bb) the Secretary does not receive a response as specified under section 409I(c)(2) of that
Act; and
(iii)(I) the Secretary certifies under subparagraph (B) that there are insufficient funds under
sections 409I and 499 of the Public Health Service Act (42 U.S.C. 284m, 290b) to conduct the
study; or
(II) the Secretary publishes in the Federal Register a certification that certifies that--
(aa) no contract or grant has been awarded under section 409I or 499 of the Public Health
Service Act (42 U.S.C. 284m, 290b); and
(bb) not less than 270 days have passed since the date of a certification under subparagraph
(B) that there are sufficient funds to conduct the study.
(B) NO AGREEMENT TO REQUEST- Not later than 60 days after determining that no holder
will agree to the written request (including a determination that the Secretary has not received
a response specified under section 505A(d) of this Act or section 409I of the Public Health
Service Act (42 U.S.C. 284m), the Secretary shall certify whether the Secretary has sufficient
funds to conduct the study under section 409I or 499 of the Public Health Service Act (42
U.S.C. 284m, 290b), taking into account the prioritization under section 409I.
(c) MEANINGFUL THERAPEUTIC BENEFIT- For the purposes of paragraph (4)(A)(iii)(I) and
(4)(B)(iii)(I) of subsection (a) and paragraphs (1)(B)(i) and (2)(B)(iii)(I)(aa) of subsection (b), a
drug or biological product shall be considered to represent a meaningful therapeutic benefit
over existing therapies if the Secretary estimates that--
(1) if approved, the drug or biological product would represent a significant improvement in the
treatment, diagnosis, or prevention of a disease, compared with marketed products
adequately labeled for that use in the relevant pediatric population; or
(2) the drug or biological product is in a class of products or for an indication for which there is
a need for additional options.
(d) SUBMISSION OF ASSESSMENTS- If a person fails to submit an assessment described in
subsection (a)(2), or a request for approval of a pediatric formulation described in subsection
(a) or (b), in accordance with applicable provisions of subsections (a) and (b)--
(1) the drug or biological product that is the subject of the assessment or request may be
considered misbranded solely because of that failure and subject to relevant enforcement
action (except that the drug or biological product shall not be subject to action under section
303); but
(2) the failure to submit the assessment or request shall not be the basis for a proceeding--
(A) to withdraw approval for a drug under section 505(e); or
(B) to revoke the license for a biological product under section 351 of the Public Health Service
Act (42 U.S.C. 262).
(e) MEETINGS- Before and during the investigational process for a new drug or biological
product, the Secretary shall meet at appropriate times with the sponsor of the new drug or
biological product to discuss--
(1) information that the sponsor submits on plans and timelines for pediatric studies; or
(2) any planned request by the sponsor for waiver or deferral of pediatric studies.
(f) SCOPE OF AUTHORITY- Nothing in this section provides to the Secretary any authority to
require a pediatric assessment of any drug or biological product, or any assessment regarding
other populations or uses of a drug or biological product, other than the pediatric assessments
described in this section.
(g) ORPHAN DRUGS- Unless the Secretary requires otherwise by regulation, this section
does not apply to any drug for an indication for which orphan designation has been granted
under section 526.
(h) INTEGRATION WITH OTHER PEDIATRIC STUDIES- The authority under this section
shall remain in effect so long as an application subject to this section may be accepted for filing
by the Secretary on or before the date specified in section 505A(n).
SEC. 506. [21 U.S.C. 356] FAST TRACK PRODUCTS.
(a) DESIGNATION OF DRUG AS A FAST TRACK PRODUCT.—
(1) IN GENERAL.—The Secretary shall, at the request of the sponsor of a new drug, facilitate
the development and expedite the review of such drug if it is intended for the treatment of a
serious or life-threatening condition and it demonstrates the potential to address unmet
medical needs for such a condition. (In this section, such a drug is referred to as a ‘‘fast track
product’’.)
(2) REQUEST FOR DESIGNATION.—The sponsor of a new drug may request the Secretary
to designate the drug as a fast track product. A request for the designation may be made
concurrently with, or at any time after, submission of an application for the investigation of the
drug under section 505(i) or section 351(a)(3) of the Public Health Service Act.
(3) DESIGNATION.—Within 60 calendar days after the receipt of a request under paragraph
(2), the Secretary shall determine whether the drug that is the subject of the request meets the
criteria described in paragraph (1). If the Secretary finds that the drug meets the criteria, the
Secretary shall designate the drug as a fast track product and shall take such actions as are
appropriate to expedite the development and review of the application for approval of such
product.
(b) APPROVAL OF APPLICATION FOR A FAST TRACK PRODUCT.—
(1) IN GENERAL.—The Secretary may approve an application for approval of a fast track
product under section 505(c) or section 351 of the Public Health Service Act upon a
determination that the product has an effect on a clinical endpoint or on a surrogate endpoint
that is reasonably likely to predict clinical benefit.
(2) LIMITATION.—Approval of a fast track product under this subsection may be subject to the
requirements—
(A) that the sponsor conduct appropriate post-approval studies to validate the surrogate
endpoint or otherwise confirm the effect on the clinical endpoint; and
(B) that the sponsor submit copies of all promotional materials related to the fast track product
during the preapproval review period and, following approval and for such period thereafter as
the Secretary determines to be appropriate, at least 30 days prior to dissemination of the
materials.
(3) EXPEDITED WITHDRAWAL OF APPROVAL.—The Secretary may withdraw approval of a
fast track product using expedited procedures (as prescribed by the Secretary in regulations
which shall include an opportunity for an informal hearing) if—
(A) the sponsor fails to conduct any required post-approval study of the fast track drug with
due diligence;
(B) a post-approval study of the fast track product fails to verify clinical benefit of the product;
(C) other evidence demonstrates that the fast track product is not safe or effective under the
conditions of use; or
(D) the sponsor disseminates false or misleading promotional materials with respect to the
product.
(c) REVIEW OF INCOMPLETE APPLICATIONS FOR APPROVAL OF A FAST TRACK
PRODUCT.—
(1) IN GENERAL.—If the Secretary determines, after preliminary evaluation of clinical data
submitted by the sponsor, that a fast track product may be effective, the Secretary shall
evaluate for filing, and may commence review of portions of, an application for the approval of
the product before the sponsor submits a complete application. The Secretary shall
commence such review only if the applicant—
(A) provides a schedule for submission of information necessary to make the application
complete; and
(B) pays any fee that may be required under section 736.
(2) EXCEPTION.—Any time period for review of human drug applications that has been
agreed to by the Secretary and that has been set forth in goals identified in letters of the
Secretary (relating to the use of fees collected under section 736 to expedite the drug
development process and the review of human drug applications) shall not apply to an
application submitted under paragraph (1) until the date on which the application is complete.
(d) AWARENESS EFFORTS.—The Secretary shall—
(1) develop and disseminate to physicians, patient organizations, pharmaceutical and
biotechnology companies, and other appropriate persons a description of the provisions of this
section applicable to fast track products; and
(2) establish a program to encourage the development of surrogate endpoints that are
reasonably likely to predict clinical benefit for serious or life-threatening conditions for which
there exist significant unmet medical needs.
SEC. 506A. [ 21 U.S.C. 356a] MANUFACTURING CHANGES.
(a) IN GENERAL.—With respect to a drug for which there is in effect an approved application
under section 505 or 512 or a license under section 351 of the Public Health Service Act, a
change from the manufacturing process approved pursuant to such application or license may
be made, and the drug as made with the change may be distributed, if—
(1) the holder of the approved application or license (referred to in this section as a ‘‘holder’’)
has validated the effects of the change in accordance with subsection (b); and
(2)(A) in the case of a major manufacturing change, the holder has complied with the
requirements of subsection (c); or
(B) in the case of a change that is not a major manufacturing change, the holder complies with
the applicable requirements of subsection (d).
(b) VALIDATION OF EFFECTS OF CHANGES.—For purposes of subsection (a)(1), a drug
made with a manufacturing change (whether a major manufacturing change or otherwise) may
be distributed only if, before distribution of the drug as so made, the holder involved validates
the effects of the change on the identity, strength, quality, purity, and potency of the drug as
the identity, strength, quality, purity, and potency may relate to the safety or effectiveness of
the drug.
(c) MAJOR MANUFACTURING CHANGES.—
(1) REQUIREMENT OF SUPPLEMENTAL APPLICATION.—For purposes of subsection
(a)(2)(A), a drug made with a major manufacturing change may be distributed only if, before
the distribution of the drug as so made, the holder involved submits to the Secretary a
supplemental application for such change and the Secretary approves the application. The
application shall contain such information as the Secretary determines to be appropriate, and
shall include the information developed under subsection (b) by the holder in validating the
effects of the change.
(2) CHANGES QUALIFYING AS MAJOR CHANGES.—For purposes of subsection (a)(2)(A),
a major manufacturing change is a manufacturing change that is determined by the Secretary
to have substantial potential to adversely affect the identity, strength, quality, purity, or potency
of the drug as they may relate to the safety or effectiveness of a drug. Such a change includes
a change that—
(A) is made in the qualitative or quantitative formulation of the drug involved or in the
specifications in the approved application or license referred to in subsection (a) for the drug
(unless exempted by the Secretary by regulation or guidance from the requirements of this
subsection);
(B) is determined by the Secretary by regulation or guidance to require completion of an
appropriate clinical study demonstrating equivalence of the drug to the drug as manufactured
without the change; or
(C) is another type of change determined by the Secretary by regulation or guidance to have a
substantial potential to adversely affect the safety or effectiveness of the drug.
(d) OTHER MANUFACTURING CHANGES.—
(1) IN GENERAL.—For purposes of subsection (a)(2)(B), the Secretary may regulate drugs
made with manufacturing changes that are not major manufacturing changes as follows:
(A) The Secretary may in accordance with paragraph (2) authorize holders to distribute such
drugs without submitting a supplemental application for such changes.
(B) The Secretary may in accordance with paragraph (3) require that, prior to the distribution of
such drugs, holders submit to the Secretary supplemental applications for such changes.
(C) The Secretary may establish categories of such changes and designate categories to
which subparagraph (A) applies and categories to which subparagraph (B) applies.
(2) CHANGES NOT REQUIRING SUPPLEMENTAL APPLICATION.—
(A) SUBMISSION OF REPORT.—A holder making a manufacturing change to which
paragraph (1)(A) applies shall submit to the Secretary a report on the change, which shall
contain such information as the Secretary determines to be appropriate, and which shall
include the information developed under subsection (b) by the holder in validating the effects
of the change. The report shall be submitted by such date as the Secretary may specify.
(B) AUTHORITY REGARDING ANNUAL REPORTS.—In the case of a holder that during a
single year makes more than one manufacturing change to which paragraph (1)(A) applies,
the Secretary may in carrying out subparagraph (A) authorize the holder to comply with such
subparagraph by submitting a single report for the year that provides the information required
in such subparagraph for all the changes made by the holder during the year.
(3) CHANGES REQUIRING SUPPLEMENTAL APPLICATION.—
(A) SUBMISSION OF SUPPLEMENTAL APPLICATION.—The supplemental application
required under paragraph (1)(B) for a manufacturing change shall contain such information as
the Secretary determines to be appropriate, which shall include the information developed
under subsection (b) by the holder in validating the effects of the change.
(B) AUTHORITY FOR DISTRIBUTION.—In the case of a manufacturing change to which
paragraph (1)(B) applies:
(i) The holder involved may commence distribution of the drug involved 30 days after the
Secretary receives the supplemental application under such paragraph, unless the Secretary
notifies the holder within such 30-day period that prior approval of the application is required
before distribution may be commenced.
(ii) The Secretary may designate a category of such changes for the purpose of providing that,
in the case of a change that is in such category, the holder involved may commence
distribution of the drug involved upon the receipt by the Secretary of a supplemental
application for the change.
(iii) If the Secretary disapproves the supplemental application, the Secretary may order the
manufacturer to cease the distribution of the drugs that have been made with the
manufacturing change.
SEC. 506B. [ 21 U.S.C. 356b] REPORTS OF POSTMARKETING STUDIES.
(a) SUBMISSION.—
(1) IN GENERAL.—A sponsor of a drug that has entered into an agreement with the Secretary
to conduct a postmarketing study of a drug shall submit to the Secretary, within 1 year after the
approval of such drug and annually thereafter until the study is completed or terminated, a
report of the progress of the study or the reasons for the failure of the sponsor to conduct the
study. The report shall be submitted in such form as is prescribed by the Secretary in
regulations issued by the Secretary.
(2) AGREEMENTS PRIOR TO EFFECTIVE DATE.—Any agreement entered into between the
Secretary and a sponsor of a drug, prior to the date of enactment of the Food and Drug
Administration Modernization Act of 1997, to conduct a postmarketing study of a drug shall be
subject to the requirements of paragraph (1). An initial report for such an agreement shall be
submitted within 6 months after the date of the issuance of the regulations under paragraph
(1).
(b) CONSIDERATION OF INFORMATION AS PUBLIC INFORMATION.— Any information
pertaining to a report described in subsection (a) shall be considered to be public information
to the extent that the information is necessary—
(1) to identify the sponsor; and
(2) to establish the status of a study described in subsection (a) and the reasons, if any, for any
failure to carry out the study.
(c) STATUS OF STUDIES AND REPORTS.—The Secretary shall annually develop and
publish in the Federal Register a report that provides information on the status of the
postmarketing studies—
(1) that sponsors have entered into agreements to conduct; and
(2) for which reports have been submitted under subsection (a)(1).
(d) DISCLOSURE.—If a sponsor fails to complete an agreed upon study required by this
section by its original or otherwise negotiated deadline, the Secretary shall publish a statement
on the Internet site of the Food and Drug Administration stating that the study was not
completed and, if the reasons for such failure to complete the study were not satisfactory to the
Secretary, a statement that such reasons were not satisfactory to the Secretary.
(e) NOTIFICATION.—With respect to studies of the type required under section 506(b)(2)(A)
or under section 314.510 or 601.41 of title 21, Code of Federal Regulations, as each of such
sections was in effect on the day before the effective date 29 of this subsection, the Secretary
may require that a sponsor who, for reasons not satisfactory to the Secretary, fails to complete
by its deadline a study under any of such sections of such type for a drug or biological product
(including such a study conducted after such effective date) notify practitioners who prescribe
such drug or biological product of the failure to complete such study and the questions of
clinical benefit, and, where appropriate, questions of safety, that remain unanswered as a
result of the failure to complete such study. Nothing in this subsection shall be construed as
altering the requirements of the types of studies required under section 506(b)(2)(A) or under
section 314.510 or 601.41 of title 21, Code of Federal Regulations, as so in effect, or as
prohibiting the Secretary from modifying such sections of title 21 of such Code to provide for
studies in addition to those of such type..
SEC. 506C. [ 21 U.S.C. 356c] DISCONTINUANCE OF A LIFE SAVING PRODUCT.
(a) IN GENERAL.—A manufacturer that is the sole manufacturer of a drug—
(1) that is—
(A) life-supporting;
(B) life-sustaining; or
(C) intended for use in the prevention of a debilitating disease or condition;
(2) for which an application has been approved under section 505(b) or 505(j); and
(3) that is not a product that was originally derived from human tissue and was replaced by a
recombinant product, shall notify the Secretary of a discontinuance of the manufacture of the
drug at least 6 months prior to the date of the discontinuance.
(b) REDUCTION IN NOTIFICATION PERIOD.—The notification period required under
subsection (a) for a manufacturer may be reduced if the manufacturer certifies to the Secretary
that good cause exists for the reduction, such as a situation in which—
(1) a public health problem may result from continuation of the manufacturing for the 6-month
period;
(2) a biomaterials shortage prevents the continuation of the manufacturing for the 6-month
period;
(3) a liability problem may exist for the manufacturer if the manufacturing is continued for the
6-month period;
(4) continuation of the manufacturing for the 6-month period may cause substantial economic
hardship for the manufacturer;
(5) the manufacturer has filed for bankruptcy under chapter 7 or 11 of title 11, United States
Code; or
(6) the manufacturer can continue the distribution of the drug involved for 6 months.
(c) DISTRIBUTION.—To the maximum extent practicable, the Secretary shall distribute
information on the discontinuation of the drugs described in subsection (a) to appropriate
physician and patient organizations.
[Section 507 repealed by Pub. L. 105–115, November 21, 1997.]
AUTHORITY TO DESIGNATE OFFICIAL NAMES
SEC. 508. 30 [21 U.S.C. 358] (a) The Secretary may designate an official name for any drug or
device if he determines that such action is necessary or desirable in the interest of usefulness
and simplicity. Any official name designated under this section for any drug or device shall be
the only official name of that drug or device used in any official compendium published after
such name has been prescribed or for any other purpose of this Act. In no event, however,
shall the Secretary establish an official name so as to infringe a valid trademark.
(b) Within a reasonable time after the effective date of this section, and at such other times as
he may deem necessary, the Secretary shall cause a review to be made of the official names
by which drugs are identified in the official United States Pharmacopeia, the official
Homeopathic Pharmacopeia of the United States, and the official National Formulary, and all
supplements thereto, and at such times as he may deem necessary shall cause a review to be
made of the official names by which devices are identified in any official compendium (and all
supplements thereto) to determine whether revision of any of those names is necessary or
desirable in the interest of usefulness and simplicity.
(c) Whenever he determines after any such review that (1) any such official name is unduly
complex or is not useful for any other reason, (2) two or more official names have been applied
to a single drug or device, or to two or more drugs which are identical in chemical structure and
pharmacological action and which are substantially identical in strength, quality, and purity, or
to two or more devices which are substantially equivalent in design and purpose or (3) no
official name has been applied to a medically useful drug or device, he shall transmit in writing
to the compiler of each official compendium in which that drug or drugs or device are identified
and recognized his request for the recommendation of a single official name for such drug or
drugs or device which will have usefulness and simplicity. Whenever such a single official
name has not been recommended within one hundred and eighty days after such request, or
the Secretary determines that any name so recommended is not useful for any reason, he
shall designate a single official name for such drug or drugs or device. Whenever he
determines that the name so recommended is useful, he shall designate that name as the
official name of such drug or drugs or device. Such designation shall be made as a regulation
upon public notice and in accordance with the procedure set forth in section 553 of title 5,
United States Code.
(d) After each such review, and at such other times as the Secretary may determine to be
necessary or desirable, the Secretary shall cause to be compiled, published, and publicly
distributed a list which shall list all revised official names of drugs or devices designated under
this section and shall contain such descriptive and explanatory matter as the Secretary may
determine to be required for the effective use of those names.
(e) Upon a request in writing by any compiler of any official compendium that the Secretary
exercise the authority granted to him under section 508(a), he shall upon public notice and in
accordance with the procedure set forth in section 553 of title 5, United States Code designate
the official name of the drug or device for which the request is made.
NONAPPLICABILITY TO COSMETICS
SEC. 509. [21 U.S.C. 359]This chapter, as amended by the Drug Amendments of 1962, shall
not apply to any cosmetic unless such cosmetic is also a drug or device or component thereof.
REGISTRATION OF PRODUCERS OF DRUGS AND DEVICES 31
SEC. 510. [21 U.S.C. 360] (a) As used in this section—
(1) the term ‘‘manufacture, preparation, propagation, compounding, or processing’’ shall
include repackaging or otherwise changing the container, wrapper, or labeling of any drug
package or device package in furtherance of the distribution of the drug or device from the
original place of manufacture to the person who makes final delivery or sale to the ultimate
consumer or user; and
(2) the term ‘‘name’’ shall include in the case of a partnership the name of each partner and, in
the case of a corporation, the name of each corporate officer and director, and the State of
incorporation.
(b) On or before December 31 of each year every person who owns or operates any
establishment in any State engaged in the manufacture, preparation, propagation,
compounding, or processing of a drug or drugs or a device or devices shall register with the
Secretary his name, places of business, and all such establishments.
(c) Every person upon first engaging in the manufacture, preparation, propagation,
compounding, or processing of a drug or drugs or a device or devices in any establishment
which he owns or operates in any State shall immediately register with the Secretary his name,
place of business, and such establishment.
(d) Every person duly registered in accordance with the foregoing subsections of this section
shall immediately register with the Secretary any additional establishment which he owns or
operates in any State and in which he begins the manufacture, preparation, propagation,
compounding, or processing of a drug or drugs or a device or devices.
(e) The Secretary may assign a registration number to any person or any establishment
registered in accordance with this section. The Secretary may also assign a listing number to
each drug or class of drugs listed under subsection (j). Any number assigned pursuant to the
preceding sentence shall be the same as that assigned pursuant to the National Drug Code.
The Secretary may by regulation prescribe a uniform system for the identification of devices
intended for human use and may require that persons who are required to list such devices
pursuant to subsection (j) shall list such devices in accordance with such system.
(f) The Secretary shall make available for inspection, to any person so requesting, any
registration filed pursuant to this section; except that any list submitted pursuant to paragraph
(3) of subsection (j) and the information accompanying any list or notice filed under paragraph
(1) or (2) of that subsection shall be exempt from such inspection unless the Secretary finds
that such an exemption would be inconsistent with protection of the public health.
(g) The foregoing subsections of this section shall not apply to—
(1) pharmacies which maintain establishments in conformance with any applicable local laws
regulating the practice of pharmacy and medicine and which are regularly engaged in
dispensing prescription drugs or devices, upon prescriptions of practitioners licensed to
administer such drugs or devices to patients under the care of such practitioners in the course
of their professional practice, and which do not manufacture, prepare, propagate, compound,
or process drugs or devices for sale other than in the regular course of their business of
dispensing or selling drugs or devices at retail;
(2) practitioners licensed by law to prescribe or administer drugs or devices and who
manufacture, prepare, propagate, compound, or process drugs or devices solely for use in the
course of their professional practice;
(3) persons who manufacture, prepare, propagate, compound, or process drugs or devices
solely for use in research, teaching, or chemical analysis and not for sale;
(4) any distributor who acts as a wholesale distributor of devices, and who does not
manufacture, repackage, process, or relabel a device; or
(5) such other classes of persons as the Secretary may by regulation exempt from the
application of this section upon a finding that registration by such classes of persons in
accordance with this section is not necessary for the protection of the public health.
In this subsection, the term ‘‘wholesale distributor’’ means any person (other than the
manufacturer or the initial importer) who distributes a device from the original place of
manufacture to the person who makes the final delivery or sale of the device to the ultimate
consumer or user.
(h) Every establishment in any State registered with the Secretary pursuant to this section
shall be subject to inspection pursuant to section 704 and every such establishment engaged
in the manufacture, propagation, compounding, or processing of a drug or drugs or of a device
or devices classified in class II or III shall be so inspected by one or more officers or
employees duly designated by the Secretary , or by persons accredited to conduct inspections
under section 704(g), at least once in the 2-year period beginning with the date of registration
of such establishment pursuant to this section and at least once in every successive 2-year
period thereafter.
(i)(1) On or before December 31 of each year, any establishment within any foreign country
engaged in the manufacture, preparation, propagation, compounding, or processing of a drug
or a device that is imported or offered for import into the United States shall, through electronic
means in accordance with the criteria of the Secretary, register with the Secretary the name
and place of business of the establishment, the name of the United States agent for the
establishment, the name of each importer of such drug or device in the United States that is
known to the establishment, and the name of each person who imports or offers for import
such drug or device to the United States for purposes of importation.
(2) The establishment shall also provide the information required by subsection (j).
(3) The Secretary is authorized to enter into cooperative arrangements with officials of foreign
countries to ensure that adequate and effective means are available for purposes of
determining, from time to time, whether drugs or devices manufactured, prepared, propagated,
compounded, or processed by an establishment described in paragraph (1), if imported or
offered for import into the United States, shall be refused admission on any of the grounds set
forth in section 801(a).
(j)(1) Every person who registers with the Secretary under subsection (b), (c), (d) or (i) shall, at
the time of registration under any such subsection, file with the Secretary a list of all drugs and
a list of all devices and a brief statement of the basis for believing that each device included in
the list is a device rather than a drug (with each drug and device in each list listed by its
established name (as defined in section 502(e)) and by any proprietary name) which are being
manufactured, prepared, propagated, compounded, or processed by him for commercial
distribution and which he has not included in any list of drugs or devices filed by him with the
Secretary under this paragraph or paragraph (2) before such time of registration. Such list
shall be prepared in such form and manner as the Secretary may prescribe and shall be
accompanied by—
(A) in the case of a drug contained in the applicable list and subject to section 505 or 512, or a
device intended for human use contained in the applicable list with respect to which a
performance standard has been established under section 514 or which is subject to section
515, a reference to the authority for the marketing of such drug or device and a copy of all
labeling for such drug or device;
(B) in the case of any other drug or device contained in an applicable list—
(i) which drug is subject to section 503(b)(1), or which device is a restricted device, a copy of
all labeling for such drug or device, a representative sampling of advertisements for such drug
or device, and, upon request made by the Secretary for good cause, a copy of all
advertisements for a particular drug product or device, or
(ii) which drug is not subject to section 503(b)(1) or which device is not a restricted device, the
label and package insert for such drug or device and a representative sampling of any other
labeling for such drug or device;
(C) in the case of any drug contained in an applicable list which is described in subparagraph
(B), a quantitative listing of its active ingredient or ingredients, except that with respect to a
particular drug product the Secretary may require the submission of a quantitative listing of all
ingredients if he finds that such submission is necessary to carry out the purposes of this Act;
and
(D) if the registrant filing a list has determined that a particular drug product or device
contained in such list is not subject to section 505 or 512, or the particular device contained in
such list is not subject to a performance standard established under section 514 or to section
515 or is not a restricted device, a brief statement of the basis upon which the registrant made
such determination if the Secretary requests such a statement with respect to that particular
drug product or device.
(2) Each person who registers with the Secretary under this section shall report to the
Secretary once during the month of June of each year and once during the month of
December of each year the following information:
(A) A list of each drug or device introduced by the registrant for commercial distribution which
has not been included in any list previously filed by him with the Secretary under this
subparagraph or paragraph (1) of this subsection. A list under this subparagraph shall list a
drug or device by its established name (as defined in section 502(e)) and by any proprietary
name it may have and shall be accompanied by the other information required by paragraph
(1).
(B) If since the date the registrant last made a report under this paragraph (or if he has not
made a report under this paragraph, since the effective date of this subsection 32 ) he has
discontinued the manufacture, preparation, propagation, compounding, or processing for
commercial distribution of a drug or device included in a list filed by him under subparagraph
(A) or paragraph (1); notice of such discontinuance, the date of such discontinuance, and the
identity (by established name (as defined in section 502(e)) and by any proprietary name) of
such drug or device.
(C) If since the date the registrant reported pursuant to subparagraph (B) a notice of
discontinuance he has resumed the manufacture, preparation, propagation, compounding, or
processing for commercial distribution of the drug or device with respect to which such notice
of discontinuance was reported; notice of such resumption, the date of such resumption, the
identity of such drug or device (by established name (as defined in section 502(e)) and by any
proprietary name), and the other information required by paragraph (1), unless the registrant
has previously reported such resumption to the Secretary pursuant to this subparagraph.
(D) Any material change in any information previously submitted pursuant to this paragraph or
paragraph (1).
(3) The Secretary may also require each registrant under this section to submit a list of each
drug product which (A) the registrant is manufacturing, preparing, propagating, compounding,
or processing for commercial distribution, and (B) contains a particular ingredient. The
Secretary may not require the submission of such a list unless he has made a finding that the
submission of such a list is necessary to carry out the purposes of this Act.
(k) Each person who is required to register under this section and who proposes to begin the
introduction or delivery for introduction into interstate commerce for commercial distribution of
a device intended for human use shall, at least ninety days before making such introduction or
delivery, report to the Secretary or person who is accredited under section 523(a) (in such
form and manner as the Secretary shall by regulation prescribe)—
(1) the class in which the device is classified under section 513 or if such person determines
that the device is not classified under such section, a statement of that determination and the
basis for such person’s determination that the device is or is not so classified, and
(2) action taken by such person to comply with requirements under section 514 or 515 which
are applicable to the device.
(l) A report under subsection (k) is not required for a device intended for human use that is
exempted from the requirements of this subsection under subsection (m) or is within a type
that has been classified into class I under section 513. The exception established in the
preceding sentence does not apply to any class I device that is intended for a use which is of
substantial importance in preventing impairment of human health, or to any class I device that
presents a potential unreasonable risk of illness or injury.
(m)(1) Not later than 60 days after the date of enactment of the Food and Drug Administration
Modernization Act of 1997, the Secretary shall publish in the Federal Register a list of each
type of class II device that does not require a report under subsection (k) to provide reasonable
assurance of safety and effectiveness. Each type of class II device identified by the Secretary
as not requiring the report shall be exempt from the requirement to provide a report under
subsection (k) as of the date of the publication of the list in the Federal Register. The Secretary
shall publish such list on the Internet site of the Food and Drug Administration. The list so
published shall be updated not later than 30 days after each revision of the list by the
Secretary.
(2) Beginning on the date that is 1 day after the date of the publication of a list under this
subsection, the Secretary may exempt a class II device from the requirement to submit a
report under subsection (k), upon the Secretary’s own initiative or a petition of an interested
person, if the Secretary determines that such report is not necessary to assure the safety and
effectiveness of the device. The Secretary shall publish in the Federal Register notice of the
intent of the Secretary to exempt the device, or of the petition, and provide a 30-day period for
public comment. Within 120 days after the issuance of the notice in the Federal Register, the
Secretary shall publish an order in the Federal Register that sets forth the final determination
of the Secretary regarding the exemption of the device that was the subject of the notice. If the
Secretary fails to respond to a petition within 180 days of receiving it, the petition shall be
deemed to be granted.
(n) The Secretary shall review the report required in subsection (k) and make a determination
under section 513(f)(1) not later than 90 days after receiving the report.
(o)(1) With respect to reprocessed single-use devices for which reports are required under
subsection (k):
(A) The Secretary shall identify such devices or types of devices for which reports under such
subsection must, in order to ensure that the device is substantially equivalent to a predicate
device, include validation data, the types of which shall be specified by the Secretary,
regarding cleaning and sterilization, and functional performance demonstrating that the
single-use device will remain substantially equivalent to its predicate device after the maximum
number of times the device is reprocessed as intended by the person submitting the premarket
notification. Within six months after enactment of this subsection, the Secretary shall publish in
the Federal Register a list of the types so identified, and shall revise the list as appropriate.
Reports under subsection (k) for devices or types of devices within a type included on the list
are, upon publication of the list, required to include such validation data.
(B) In the case of each report under subsection (k) that was submitted to the Secretary before
the publication of the initial list under subparagraph (A), or any revision thereof, and was for a
device or type of device included on such list, the person who submitted the report under
subsection (k) shall submit validation data as described in subparagraph (A) to the Secretary
not later than nine months after the publication of the list. During such nine-month period, the
Secretary may not take any action under this Act against such device solely on the basis that
the validation data for the device have not been submitted to the Secretary. After the
submission of the validation data to the Secretary, the Secretary may not determine that the
device is misbranded under section 502(o), or adulterated under section 501(f)(1)(B), or take
action against the device under section 301(p) for failure to provide any information required
by subsection (k) until (i) the review is terminated by withdrawal of the submission of the report
under subsection (k); (ii) the Secretary finds the data to be acceptable and issues a letter; or (iii)
the Secretary determines that the device is not substantially equivalent to a predicate device.
Upon a determination that a device is not substantially equivalent to a predicate device, or if
such submission is withdrawn, the device can no longer be legally marketed.
(C) In the case of a report under subsection (k) for a device identified under subparagraph (A)
that is of a type for which the Secretary has not previously received a report under such
subsection, the Secretary may, in advance of revising the list under subparagraph (A) to
include such type, require that the report include the validation data specified in subparagraph
(A).
(D) Section 502(o) applies with respect to the failure of a report under subsection (k) to include
validation data required under subparagraph (A).
(2) With respect to critical or semi-critical reprocessed single-use devices that, under
subsection (l) or (m), are exempt from the requirement of submitting reports under subsection
(k):
(A) The Secretary shall identify such devices or types of devices for which such exemptions
should be terminated in order to provide a reasonable assurance of the safety and
effectiveness of the devices. <> The Secretary shall publish in the Federal Register a list of the
devices or types of devices so identified, and shall revise the list as appropriate. The
exemption for each device or type included on the list is terminated upon the publication of the
list. For each report under subsection (k) submitted pursuant to this subparagraph the
Secretary shall require the validation data described in paragraph (1)(A).
(B) For each device or type of device included on the list under subparagraph (A), a report
under subsection (k) shall be submitted to the Secretary not later than 15 months after the
publication of the initial list, or a revision of the list, whichever terminates the exemption for the
device. During such 15-month period, the Secretary may not take any action under this Act
against such device solely on the basis that such report has not been submitted to the
Secretary. After the submission of the report to the Secretary the Secretary may not determine
that the device is misbranded under section 502(o), or adulterated under section 501(f)(1)(B),
or take action against the device under section 301(p) for failure to provide any information
required by subsection (k) until (i) the review is terminated by withdrawal of the submission; (ii)
the Secretary determines by order that the device is substantially equivalent to a predicate
device; or (iii) the Secretary determines by order that the device is not substantially equivalent
to a predicate device. Upon a determination that a device is not substantially equivalent to a
predicate device, the device can no longer be legally marketed.
(C) In the case of semi-critical devices, the initial list under subparagraph (A) shall be
published not later than 18 months after the effective date of this subsection. In the case of
critical devices, the initial list under such subparagraph shall be published not later than six
months after such effective date.
(D) Section 502(o) applies with respect to the failure to submit a report under subsection (k)
that is required pursuant to subparagraph (A), including a failure of the report to include
validation data required in such subparagraph.
(E) The termination under subparagraph (A) of an exemption under subsection (l) or (m) for a
critical or semi-critical reprocessed single-use device does not terminate the exemption under
subsection (l) or (m) for the original device.
(p) Registrations under subsections (b), (c), (d), and (i) (including the submission of updated
information) shall be submitted to the Secretary by electronic means, upon a finding by the
Secretary that the electronic receipt of such registrations is feasible, unless the Secretary
grants a request for waiver of such requirement because use of electronic means is not
reasonable for the person requesting such waiver.
SEC. 511. Repealed by section 701(a) of Public Law 91-513.
Footnotes: Chapter V, Sections 501-510
1. See footnote for section 403(h)(3) regarding the stylistic use of a list consisting of "(a)",
"(b)", etc.
2. So in law. Probably should be "subparagraph".
3. See footnote for section 403(h)(3) regarding the stylistic use of a list consisting of "(a)",
"(b)", etc.
4. Paragraph (d) was struck by section 126(6) of Public Law 105-115 (111 Stat.2327).
5. Paragraph (k) was struck by section 125(a)(2)(B) of Public Law 105–115 (111 Stat. 2325).
Paragraph (l) was struck by section 125(b)(2)(D) of such Public Law.
6. 2 So in law. Probably should be "paragraph (e)".
7. So in law. Probably should be "This paragraph".
8. Sentence was added by title I of Public Law 95–633. Section 112 of such Public Law
provided as follows: "This title shall take effect on the date the Convention on Psychotropic
Substances, signed at Vienna, Austria on February 21, 1971, enters into force in respect to the
United States.". The Convention entered into force in respect to the United States on July 15,
1980.
9. Paragraph (u) was added by section 301(a) of Public Law 107–250 (116 Stat. 1616), which
was enacted October 26, 2002. Subsection (b) of such section (as amended by section 2(c)(1)
of Public Law 108–214; 118 Stat. 575) provides as follows:
(b) EFFECTIVE DATE.—The amendment made by subsection (a) takes effect 36 months after
the date of the enactment of this Act, and only applies to devices introduced or delivered for
introduction into interstate commerce after such effective date.
10. Paragraph (v) was added by section 302(a)(1) of Public Law 107–250 (116 Stat. 1616),
which was enacted October 26, 2002. Paragraph (2) of such subsection provides as follows:
(2) EFFECTIVE DATE.—The amendment made by paragraph (1) takes effect 15 months after
the date of the enactment of this Act, and only applies to devices introduced or delivered for
introduction into interstate commerce after such effective date.
11. The subsection was added by section 16(a)(2) of Public Law 101–692, which was enacted
November 28, 1990. The subsection was added as subsection (f), and was redesignated as
subsection (g) by section 2(d)(4) of Public Law 102–108.
12. Paragraph (4) was added by section 204(3) of Public Law 107–250 (116 Stat. 1611), which
was enacted October 26, 2002.
13. The amendments made to this Act by the Drug Amendments of 1962 (Public Law 87–781)
included amendments establishing the requirement that new drugs be effective. Section 107(c)
of such Public Law concerned the applicability of the amendments, and is included in the
appendix.
14. Provision was added by title I of Public Law 98–417, which was enacted September 24,
1984.
15. So in law. See section 1101(b)(2)(D) of Public Law 108–173 (117 Stat. 2454). Probably
should be "subsection (b)(3)".
16. See footnote for subsection (c)(2).
17. So in law. Probably should be "bioavailability".
18. Indentation is so in law. See section 15(c) of Public Law 107–109 (115 Stat. 1420).
19. Public Law 108–173, enacted December 8, 2003.
20. This subsection was added by title I of Public Law 98–417, which was enacted September
24, 1984.
21. 1 See footnote for clause (i).
22. See footnote for paragraph (5)(F)(i).
23. 1 See footnote for paragraph (5)(F)(i).
24. Subsection (a) of section 1103 of Public Law 108–173 (117 Stat. 2460) amended
subparagraph (A) of paragraph (8) to read as provided above, and also added to such
paragraph subparagraph (C) (see next page). Subsection (b) of such section 1103 provides as
follows: "The amendment made by subsection (a) does not alter the standards for approval of
drugs under section 505(j) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355(j)).".
25. Section 16 of Public Law 107–109 (115 Stat. 1421) requires the Comptroller General of the
United States, in consultation with the Secretary of Health and Human Services, to submit to
Congress a report that relates to section 505A and to section 409I of the Public Health Service
Act. The report is required to be submitted not later than October 1, 2006.
26. So in law. There is no section 499 in this Act. The probable intent of the Congress was to
refer to section 499 of the Public Health Service Act, which provides for a Foundation.
27. Probably should be "subsection (b) or (c)". Section 19(4) of Public Law 107–109 (115 Stat.
1424) provided in part that subsection (m) is amended by striking "subsection (a) or (c)" and
inserting ";subsection (b) or (c)". The language to be struck does not appear in subsection (m),
but does appear in subsection (n). (Subsections (m) and (n) were two of 10 subsections
redesignated by section 19(2) of such Public Law.)
28. Section 2 of Public Law 108–155 (117 Stat. 1936) added section 505B above. Section 4 of
such Act (117 Stat. 1942) provides as follows:
SEC. 4. EFFECTIVE DATE.
(a) IN GENERAL.—Subject to subsection (b), this Act and the amendments made by this Act
take effect on the date of enactment of this Act.
(b) APPLICABILITY TO NEW DRUGS AND BIOLOGICAL PRODUCTS.—
(1) IN GENERAL.—Subsection (a) of section 505B of the Federal Food, Drug, and Cosmetic
Act (as added by section 2) shall apply to an application described in paragraph (1) of that
subsection submitted to the Secretary of Health and Human Services on or after April 1, 1999.
(2) WAIVERS AND DEFERRALS.—
(A) WAIVER OR DEFERRAL GRANTED.—If, with respect to an application submitted to the
Secretary of Health and Human Services between April 1, 1999, and the date of enactment of
this Act, a waiver or deferral of pediatric assessments was granted under regulations of the
Secretary then in effect, the waiver or deferral shall be a waiver or deferral under subsection (a)
of section 505B of the Federal Food, Drug, and Cosmetic Act, except that any date specified in
such a deferral shall be extended by the number of days that is equal to the number of days
between October 17, 2002, and the date of enactment of this Act.
(B) WAIVER AND DEFERRAL NOT GRANTED.—If, with respect to an application submitted
to the Secretary of Health and Human Services between April 1, 1999, and the date of
enactment of this Act, neither a waiver nor deferral of pediatric assessments was granted
under regulations of the Secretary then in effect, the person that submitted the application
shall be required to submit assessments under subsection (a)(2) of section 505B of the
Federal Food, Drug, and Cosmetic Act on the date that is the later of—
(i) the date that is 1 year after the date of enactment of this Act; or
(ii) such date as the Secretary may specify under subsection (a)(3) of that section; unless the
Secretary grants a waiver under subsection (a)(4) of that section.
(c) NO LIMITATION OF AUTHORITY.—Neither the lack of guidance or regulations to
implement this Act or the amendments made by this Act nor the pendency of the process for
issuing guidance or regulations shall limit the authority of the Secretary of Health and Human
Services under, or defer any requirement under, this Act or those amendments.
29. Subsection (e) was added by section 506 of Public Law 107–188 (116 Stat. 693). Section
506 was contained in subtitle A of title V of the Public Law, and section 508 of that subtitle
provided that "The amendments made by this subtitle take effect October 1, 2002."
30. Section 507 was struck by section 125(b)(1) of Public Law 105–115 (111 Stat. 2325).
31. The purpose of section 510 was stated in section 301 of Public Law 82–781 as follows:
"SEC. 301. The Congress hereby finds and declares that in order to make regulation of
interstate commerce in drugs effective, it is necessary to provide for registration and inspection
of all establishments in which drugs are manufactured, prepared, propagated, compounded, or
processed; that the products of all such establishments are likely to enter the channels of
interstate commerce and directly affect such commerce; and that the regulation of interstate
commerce in drugs without provision for registration and inspection of establishments that may
be engaged only in intrastate commerce in such drugs would discriminate against and depress
interstate commerce in such drugs, and adversely burden, obstruct, and affect such interstate
commerce."
32. The effective date is February 1, 1973. This subsection was added by Public Law 92–387,
which was enacted August 16, 1972. Section 5 of such Public Law provided that the
amendments made by the Public Law "shall take effect on the first day of the sixth month
beginning after the date of the enactment of this Act.".
CHAPTER V--Drugs and Devices Subchapter A--Drugs and Devices
NEW ANIMAL DRUGS
SEC. 512. 1, 2 [21 U.S.C. 360b] (a)(1) 3 A new animal drug shall, with respect to any particular
use or intended use of such drug, be deemed unsafe for purposes of section 501(a)(5) and
section 402(a)(2)(C)(ii) unless—
(A) there is in effect an approval of an application filed pursuant to subsection (b) with respect
to such use or intended use of such drug, and such drug, its labeling, and such use conform to
such approved application;
(B) there is in effect a conditional approval of an application filed pursuant to section 571 with
respect to such use or intended use of such drug, and such drug, its labeling, and such use
conform to such conditionally approved application; or
(C) there is in effect an index listing pursuant to section 572 with respect to such use or
intended use of such drug in a minor species, and such drug, its labeling, and such use
conform to such index listing.
A new animal drug shall also be deemed unsafe for such purposes in the event of removal
from the establishment of a manufacturer, packer, or distributor of such drug for use in the
manufacture of animal feed in any State unless at the time of such removal such manufacturer,
packer, or distributor has an unrevoked written statement from the consignee of such drug, or
notice from the Secretary, to the effect that, with respect to the use of such drug in animal feed,
such consignee (i) holds a license issued under subsection (m) and has in its possession
current approved labeling for such drug in animal feed; or (ii) will, if the consignee is not a user
of the drug, ship such drug only to a holder of a license issued under subsection (m).
(2) An animal feed bearing or containing a new animal drug shall, with respect to any particular
use or intended use of such animal feed be deemed unsafe for purposes of section 501(a)(6)
unless—
(A) there is in effect—
(i) an approval of an application filed pursuant to subsection (b) with respect to such drug, as
used in such animal feed, and such animal feed and its labeling, distribution, holding, and use
conform to such approved application;
(ii) a conditional approval of an application filed pursuant to section 571 with respect to such
drug, as used in such animal feed, and such animal feed and its labeling, distribution, holding,
and use conform to such conditionally approved application; or
(iii) an index listing pursuant to section 572 with respect to such drug, as used in such animal
feed, and such animal feed and its labeling, distribution, holding, and use conform to such
index listing; and
(B) such animal feed is manufactured at a site for which there is in effect a license issued
pursuant to subsection (m)(1) to manufacture such animal feed.
(3) A new animal drug or an animal feed bearing or containing a new animal drug shall not be
deemed unsafe for the purposes of section 501(a)(5) or (6) if such article is for investigational
use and conforms to the terms of an exemption in effect with respect thereto under section
512(j).
(4) (A) Except as provided in subparagraph (B), if an approval of an application filed under
subsection (b) is in effect with respect to a particular use or intended use of a new animal drug,
the drug shall not be deemed unsafe for the purposes of paragraph (1) and shall be exempt
from the requirements of section 502(f) with respect to a different use or intended use of the
drug, other than a use in or on animal feed, if such use or intended use—
(i) is by or on the lawful written or oral order of a licensed veterinarian within the context of a
veterinarian-client-patient relationship, as defined by the Secretary; and
(ii) is in compliance with regulations promulgated by the Secretary that establish the conditions
for such different use or intended use.
The regulations promulgated by the Secretary under clause (ii) may prohibit particular uses of
an animal drug and shall not permit such different use of an animal drug if the labeling of
another animal drug that contains the same active ingredient and which is in the same dosage
form and concentration provides for such different use.
(B) If the Secretary finds that there is a reasonable probability that a use of an animal drug
authorized under subparagraph (A) may present a risk to the public health, the Secretary
may—
(i) establish a safe level for a residue of an animal drug when it is used for such different use
authorized by subparagraph (A); and
(ii) require the development of a practical, analytical method for the detection of residues of
such drug above the safe level established under clause (i).
The use of an animal drug that results in residues exceeding a safe level established under
clause (i) shall be considered an unsafe use of such drug under paragraph (1). Safe levels
may be established under clause (i) either by regulation or order.
(C) The Secretary may by general regulation provide access to the records of veterinarians to
ascertain any use or intended use authorized under subparagraph (A) that the Secretary has
determined may present a risk to the public health.
(D) If the Secretary finds, after affording an opportunity for public comment, that a use of an
animal drug authorized under subparagraph (A) presents a risk to the public health or that an
analytical method required under subparagraph (B) has not been developed and submitted to
the Secretary, the Secretary may, by order, prohibit any such use.
(5) If the approval of an application filed under section 505 is in effect, the drug under such
application shall not be deemed unsafe for purposes of paragraph (1) and shall be exempt
from the requirements of section 502(f) with respect to a use or intended use of the drug in
animals if such use or intended use—
(A) is by or on the lawful written or oral order of a licensed veterinarian within the context of a
veterinarian-client-patient relationship, as defined by the Secretary; and
(B) is in compliance with regulations promulgated by the Secretary that establish the
conditions for the use or intended use of the drug in animals.
(6) For purposes of section 402(a)(2)(D), a use or intended use of a new animal drug shall not
be deemed unsafe under this section if the Secretary establishes a tolerance for such drug
and any edible portion of any animal imported into the United States does not contain residues
exceeding such tolerance. In establishing such tolerance, the Secretary shall rely on data
sufficient to demonstrate that a proposed tolerance is safe based on similar food safety criteria
used by the Secretary to establish tolerances for applications for new animal drugs filed under
subsection (b)(1). The Secretary may consider and rely on data submitted by the drug
manufacturer, including data submitted to appropriate regulatory authorities in any country
where the new animal drug is lawfully used or data available from a relevant international
organization, to the extent such data are not inconsistent with the criteria used by the
Secretary to establish a tolerance for applications for new animal drugs filed under subsection
(b)(1). For purposes of this paragraph, ‘‘relevant international organization’’ means the Codex
Alimenterius Commission or other international organization deemed appropriate by the
Secretary. The Secretary may, under procedures specified by regulation, revoke a tolerance
established under this paragraph if information demonstrates that the use of the new animal
drug under actual use conditions results in food being imported into the United States with
residues exceeding the tolerance or if scientific evidence shows the tolerance to be unsafe.
(b)(1) Any person may file with the Secretary an application with respect to any intended use
or uses of a new animal drug. Such person shall submit to the Secretary as a part of the
application (A) full reports of investigations which have been made to show whether or not
such drug is safe and effective for use; (B) a full list of the articles used as components of such
drug; (C) a full statement of the composition of such drug; (D) a full description of the methods
used in, and the facilities and controls used for, the manufacture, processing, and packing of
such drug; (E) such samples of such drug and of the articles used as components thereof, of
any animal feed for use in or on which such drug is intended, and of the edible portions or
products (before or after slaughter) of animals to which such drug (directly or in or on animal
feed) is intended to be administered, as the Secretary may require; (F) specimens of the
labeling proposed to be used for such drug, or in case such drug is intended for use in animal
feed, proposed labeling appropriate for such use, and specimens of the labeling for the drug to
be manufactured, packed, or distributed by the applicant; (G) a description of practicable
methods for determining the quantity, if any, of such drug in or on food, and any substance
formed in or on food, because of its use; and (H) the proposed tolerance or withdrawal period
or other use restrictions for such drug if any tolerance or withdrawal period or other use
restrictions are required in order to assure that the proposed use of such drug will be safe. The
applicant shall file with the application the patent number and the expiration date of any patent
which claims the new animal drug for which the applicant filed the application or which claims a
method of using such drug and with respect to which a claim of patent infringement could
reasonably be asserted if a person not licensed by the owner engaged in the manufacture, use,
or sale of the drug. If an application is filed under this subsection for a drug and a patent which
claims such drug or a method of using such drug is issued after the filing date but before
approval of the application, the applicant shall amend the application to include the information
required by the preceding sentence. Upon approval of the application, the Secretary shall
publish information submitted under the two preceding sentences.
(2) Any person may file with the Secretary an abbreviated application for the approval of a new
animal drug. An abbreviated application shall contain the information required by subsection
(n).
(3) Any person intending to file an application under paragraph (1), section 571, or a request
for an investigational exemption under subsection (j) shall be entitled to one or more
conferences prior to such submission to reach an agreement acceptable to the Secretary
establishing a submission or an investigational requirement, which may include a requirement
for a field investigation. A decision establishing a submission or an investigational requirement
shall bind the Secretary and the applicant or requestor unless (A) the Secretary and the
applicant or requestor mutually agree to modify the requirement, or (B) the Secretary by
written order determines that a substantiated scientific requirement essential to the
determination of safety or effectiveness of the animal drug involved has appeared after the
conference. No later than 25 calendar days after each such conference, the Secretary shall
provide a written order setting forth a scientific justification specific to the animal drug and
intended uses under consideration if the agreement referred to in the first sentence requires
more than one field investigation as being essential to provide substantial evidence of
effectiveness for the intended uses of the drug. Nothing in this paragraph shall be construed
as compelling the Secretary to require a field investigation.
(c)(1) Within one hundred and eighty days after the filing of an application pursuant to
subsection (b), or such additional period as may be agreed upon by the Secretary and the
applicant, the Secretary shall either (A) issue an order approving the application if he then
finds that none of the grounds for denying approval specified in subsection (d) applies, or (B)
give the applicant notice of an opportunity for a hearing before the Secretary under subsection
(d) on the question whether such application is approvable. If the applicant elects to accept the
opportunity for a hearing by written request within thirty days after such notice, such hearing
shall commence not more than ninety days after the expiration of such thirty days unless the
Secretary and the applicant otherwise agree. Any such hearing shall thereafter be conducted
on an expedited basis and the Secretary’s order thereon shall be issued within ninety days
after the date fixed by the Secretary for filing final briefs.
(2)(A) Subject to subparagraph (C), the Secretary shall approve an abbreviated application for
a drug unless the Secretary finds—
(i) the methods used in, or the facilities and controls used for, the manufacture, processing,
and packing of the drug are inadequate to assure and preserve its identity, strength, quality,
and purity;
(ii) the conditions of use prescribed, recommended, or suggested in the proposed labeling are
not reasonably certain to be followed in practice or, except as provided in subparagraph (B),
information submitted with the application is insufficient to show that each of the proposed
conditions of use or similar limitations (whether in the labeling or published pursuant to
subsection (i)) have been previously approved for the approved new animal drug referred to in
the application;
(iii) information submitted with the application is insufficient to show that the active ingredients
are the same as those of the approved new animal drug referred to in the application;
(iv)(I) if the application is for a drug whose active ingredients, route of administration, dosage
form, strength, or use with other animal drugs in animal feed is the same as the active
ingredients, route of administration, dosage form, strength, or use with other animal drugs in
animal feed of the approved new animal drug referred to in the application, information
submitted in the application is insufficient to show that the active ingredients, route of
administration, dosage form, strength, or use with other animal drugs in animal feed is the
same as that of the approved new animal drug, or
(II) if the application is for a drug whose active ingredients, route of administration, dosage
form, strength, or use with other animal drugs in animal feed is different from that of the
approved new animal drug referred to in the application, no petition to file an application for the
drug with the different active ingredients, route of administration, dosage form, strength, or use
with other animal drugs in animal feed was approved under subsection (n)(3);
(v) if the application was filed pursuant to the approval of a petition under subsection (n)(3), the
application did not contain the information required by the Secretary respecting the active
ingredients, route of administration, dosage form, strength, or use with other animal drugs in
animal feed which is not the same;
(vi) information submitted in the application is insufficient to show that the drug is bioequivalent
to the approved new animal drug referred to in the application, or if the application is filed
under a petition approved pursuant to subsection (n)(3), information submitted in the
application is insufficient to show that the active ingredients of the new animal drug are of the
same pharmacological or therapeutic class as the pharmacological or therapeutic class of the
approved new animal drug and that the new animal drug can be expected to have the same
therapeutic effect as the approved new animal drug when used in accordance with the
labeling;
(vii) information submitted in the application is insufficient to show that the labeling proposed
for the drug is the same as the labeling approved for the approved new animal drug referred to
in the application except for changes required because of differences approved under a
petition filed under subsection (n)(3), because of a different withdrawal period, or because the
drug and the approved new animal drug are produced or distributed by different
manufacturers;
(viii) information submitted in the application or any other information available to the Secretary
shows that (I) the inactive ingredients of the drug are unsafe for use under the conditions
prescribed, recommended, or suggested in the labeling proposed for the drug, (II) the
composition of the drug is unsafe under such conditions because of the type or quantity of
inactive ingredients included or the manner in which the inactive ingredients are included, or
(III) in the case of a drug for food producing animals, the inactive ingredients of the drug or its
composition may be unsafe with respect to human food safety;
(ix) the approval under subsection (b)(1) of the approved new animal drug referred to in the
application filed under subsection (b)(2) has been withdrawn or suspended for grounds
described in paragraph (1) of subsection (e), the Secretary has published a notice of a hearing
to withdraw approval of the approved new animal drug for such grounds, the approval under
this paragraph of the new animal drug for which the application under subsection (b)(2) was
filed has been withdrawn or suspended under subparagraph (G) for such grounds, or the
Secretary has determined that the approved new animal drug has been withdrawn from sale
for safety or effectiveness reasons;
(x) the application does not meet any other requirement of subsection (n); or
(xi) the application contains an untrue statement of material fact.
(B) If the Secretary finds that a new animal drug for which an application is submitted under
subsection (b)(2) is bioequivalent to the approved new animal drug referred to in such
application and that residues of the new animal drug are consistent with the tolerances
established for such approved new animal drug but at a withdrawal period which is different
than the withdrawal period approved for such approved new animal drug, the Secretary may
establish, on the basis of information submitted, such different withdrawal period as the
withdrawal period for the new animal drug for purposes of the approval of such application for
such drug.
(C) Within 180 days of the initial receipt of an application under subsection (b)(2) or within such
additional period as may be agreed upon by the Secretary and the applicant, the Secretary
shall approve or disapprove the application.
(D) The approval of an application filed under subsection (b)(2) shall be made effective on the
last applicable date determined under the following:
(i) If the applicant only made a certification described in clause (i) or (ii) of subsection (n)(1)(G)
or in both such clauses, the approval may be made effective immediately.
(ii) If the applicant made a certification described in clause (iii) of subsection (n)(1)(G), the
approval may be made effective on the date certified under clause (iii).
(iii) If the applicant made a certification described in clause (iv) of subsection (n)(1)(G), the
approval shall be made effective immediately unless an action is brought for infringement of a
patent which is the subject of the certification before the expiration of 45 days from the date the
notice provided under subsection (n)(2)(B)(i) is received. If such an action is brought before
the expiration of such days, the approval shall be made effective upon the expiration of the 30
month period beginning on the date of the receipt of the notice provided under subsection
(n)(2)(B) or such shorter or longer period as the court may order because either party to the
action failed to reasonably cooperate in expediting the action, except that if before the
expiration of such period—
(I) the court decides that such patent is invalid or not infringed, the approval shall be made
effective on the date of the court decision,
(II) the court decides that such patent has been infringed, the approval shall be made effective
on such date as the court orders under section 271(e)(4)(A) of title 35, United States Code, or
(III) the court grants a preliminary injunction prohibiting the applicant from engaging in the
commercial manufacture or sale of the drug until the court decides the issues of patent validity
and infringement and if the court decides that such patent is invalid or not infringed, the
approval shall be made effective on the date of such court decision.
In such an action, each of the parties shall reasonably cooperate in expediting the action. Until
the expiration of 45 days from the date the notice made under subsection (n)(2)(B) is received,
no action may be brought under section 2201 of title 28, United States Code, for a declaratory
judgment with respect to the patent. Any action brought under section 2201 shall be brought in
the judicial district where the defendant has its principal place of business or a regular and
established place of business.
(iv) If the application contains a certification described in clause (iv) of subsection (n)(1)(G) and
is for a drug for which a previous application has been filed under this subsection containing
such a certification, the application shall be made effective not earlier than 180 days after—
(I) the date the Secretary receives notice from the applicant under the previous application of
the first commercial marketing of the drug under the previous application, or
(II) the date of a decision of a court in an action described in subclause (III) 4 holding the
patent which is the subject of the certification to be invalid or not infringed, whichever is earlier.
(E) If the Secretary decides to disapprove an application, the Secretary shall give the applicant
notice of an opportunity for a hearing before the Secretary on the question of whether such
application is approvable. If the applicant elects to accept the opportunity for hearing by written
request within 30 days after such notice, such hearing shall commence not more than 90 days
after the expiration of such 30 days unless the Secretary and the applicant otherwise agree.
Any such hearing shall thereafter be conducted on an expedited basis and the Secretary’s
order thereon shall be issued within 90 days after the date fixed by the Secretary for filing final
briefs.
(F)(i) If an application submitted under subsection (b)(1) for a drug, no active ingredient
(including any ester or salt of the active ingredient) of which has been approved in any other
application under subsection (b)(1), is approved after the date of the enactment of this
paragraph 5 , no application may be submitted under subsection (b)(2) which refers to the drug
for which the subsection (b)(1) application was submitted before the expiration of 5 years from
the date of the approval of the application under subsection (b)(1), except that such an
application may be submitted under subsection (b)(2) after the expiration of 4 years from the
date of the approval of the subsection (b)(1) application if it contains a certification of patent
invalidity or noninfringement described in clause (iv) of subsection (n)(1)(G). The approval of
such an application shall be made effective in accordance with subparagraph (B) except that, if
an action for patent infringement is commenced during the one-year period beginning 48
months after the date of the approval of the subsection (b) application, the 30 month period
referred to in subparagraph (D)(iii) shall be extended by such amount of time (if any) which is
required for seven and one-half years to have elapsed from the date of approval of the
subsection (b) application.
(ii) If an application submitted under subsection (b)(1) for a drug, which includes an active
ingredient (including any ester or salt of the active ingredient) that has been approved in
another application approved under such subsection, is approved after the date of enactment
of this paragraph 5 and if such application contains substantial evidence of the effectiveness of
the drug involved, any studies of animal safety, or, in the case of food producing animals,
human food safety studies ( other than bioequivalence studies or residue depletion studies,
except residue depletion studies for minor uses or minor species) required for the approval of
the application and conducted or sponsored by the applicant, the Secretary may not make the
approval of an application submitted under subsection (b)(2) for the conditions of approval of
such drug in the subsection (b)(1) application effective before the expiration of 3 years from
the date of the approval of the application under subsection (b)(1) for such drug.
(iii) If a supplement to an application approved under subsection (b)(1) is approved after the
date of enactment of this paragraph 2 and the supplement contains substantial evidence of the
effectiveness of the drug involved, any studies of animal safety, or, in the case of food
producing animals, human food safety studies ( other than bioequivalence studies or residue
depletion studies, except residue depletion studies for minor uses or minor species) 6 required
for the approval of the supplement and conducted or sponsored by the person submitting the
supplement, the Secretary may not make the approval of an application submitted under
subsection (b)(2) for a change approved in the supplement effective before the expiration of 3
years from the date of the approval of the supplement.
(iv) An applicant under subsection (b)(1) who comes within the provisions of clause (i) of this
subparagraph as a result of an application which seeks approval for a use solely in non-food
producing animals, may elect, within 10 days of receiving such approval, to waive clause (i) of
this subparagraph, in which event the limitation on approval of applications submitted under
subsection (b)(2) set forth in clause (ii) of this subparagraph shall be applicable to the
subsection (b)(1) application.
(v) If an application (including any supplement to a new animal drug application) submitted
under subsection (b)(1) for a new animal drug for a food-producing animal use, which includes
an active ingredient (including any ester or salt of the active ingredient) which has been the
subject of a waiver under clause (iv) is approved after the date of enactment of this paragraph
7 , and if the application contains substantial evidence of the effectiveness of the drug involved,
any studies of animal safety, or human food safety studies ( other than bioequivalence studies
or residue depletion studies, except residue depletion studies for minor uses or minor species)
required for the new approval of the application and conducted or sponsored by the applicant,
the Secretary may not make the approval of an application (including any supplement to such
application) submitted under subsection (b)(2) for the new conditions of approval of such drug
in the subsection (b)(1) application effective before the expiration of five years from the date of
approval of the application under subsection (b)(1) for such drug. The provisions of this
paragraph shall apply only to the first approval for a food-producing animal use for the same
applicant after the waiver under clause (iv).
(G) If an approved application submitted under subsection (b)(2) for a new animal drug refers
to a drug the approval of which was withdrawn or suspended for grounds described in
paragraph (1) or (2) of subsection (e) or was withdrawn or suspended under this subparagraph
or which, as determined by the Secretary, has been withdrawn from sale for safety or
effectiveness reasons, the approval of the drug under this paragraph shall be withdrawn or
suspended—
(i) for the same period as the withdrawal or suspension under subsection (e) or this
subparagraph, or
(ii) if the approved new animal drug has been withdrawn from sale, for the period of withdrawal
from sale or, if earlier, the period ending on the date the Secretary determines that the
withdrawal from sale is not for safety or effectiveness reasons.
(H) For purposes of this paragraph:
(i) The term "bioequivalence" means the rate and extent to which the active ingredient or
therapeutic ingredient is absorbed from a new animal drug and becomes available at the site
of drug action.
(ii) A new animal drug shall be considered to be bioequivalent to the approved new animal
drug referred to in its application under subsection (n) if—
(I) the rate and extent of absorption of the drug do not show a significant difference from the
rate and extent of absorption of the approved new animal drug referred to in the application
when administered at the same dose of the active ingredient under similar experimental
conditions in either a single dose or multiple doses;
(II) the extent of absorption of the drug does not show a significant difference from the extent
of absorption of the approved new animal drug referred to in the application when
administered at the same dose of the active ingredient under similar experimental conditions in
either a single dose or multiple doses and the difference from the approved new animal drug in
the rate of absorption of the drug is intentional, is reflected in its proposed labeling, is not
essential to the attainment of effective drug concentrations in use, and is considered
scientifically insignificant for the drug in attaining the intended purposes of its use and
preserving human food safety; or
(III) in any case in which the Secretary determines that the measurement of the rate and extent
of absorption or excretion of the new animal drug in biological fluids is inappropriate or
impractical, an appropriate acute pharmacological effects test or other test of the new animal
drug and, when deemed scientifically necessary, of the approved new animal drug referred to
in the application in the species to be tested or in an appropriate animal model does not show
a significant difference between the new animal drug and such approved new animal drug
when administered at the same dose under similar experimental conditions.
If the approved new animal drug referred to in the application for a new animal drug under
subsection (n) is approved for use in more than one animal species, the bioequivalency
information described in subclauses (I), (II), and (III) shall be obtained for one species, or if the
Secretary deems appropriate based on scientific principles, shall be obtained for more than
one species. The Secretary may prescribe the dose to be used in determining bioequivalency
under subclause (I), (II), or (III). To assure that the residues of the new animal drug will be
consistent with the established tolerances for the approved new animal drug referred to in the
application under subsection (b)(2) upon the expiration of the withdrawal period contained in
the application for the new animal drug, the Secretary shall require bioequivalency data or
residue depletion studies of the new animal drug or such other data or studies as the Secretary
considers appropriate based on scientific principles. If the Secretary requires one or more
residue studies under the preceding sentence, the Secretary may not require that the assay
methodology used to determine the withdrawal period of the new animal drug be more
rigorous than the methodology used to determine the withdrawal period for the approved new
animal drug referred to in the application. If such studies are required and if the approved new
animal drug, referred to in the application for the new animal drug for which such studies are
required, is approved for use in more than one animal species, such studies shall be
conducted for one species, or if the Secretary deems appropriate based on scientific principles,
shall be conducted for more than one species.
(3) If the patent information described in subsection (b)(1) could not be filed with the
submission of an application under subsection (b)(1) because the application was filed before
the patent information was required under subsection (b)(1) or a patent was issued after the
application was approved under such subsection, the holder of an approved application shall
file with the Secretary the patent number and the expiration date of any patent which claims
the new animal drug for which the application was filed or which claims a method of using such
drug and with respect to which a claim of patent infringement could reasonably be asserted if a
person not licensed by the owner engaged in the manufacture, use, or sale of the drug. If the
holder of an approved application could not file patent information under subsection (b)(1)
because it was not required at the time the application was approved, the holder shall file such
information under this subsection not later than 30 days after the date of the enactment of this
sentence 8 , and if the holder of an approved application could not file patent information under
subsection (b)(1) because no patent had been issued when an application was filed or
approved, the holder shall file such information under this subsection not later than 30 days
after the date the patent involved is issued. Upon the submission of patent information under
this subsection, the Secretary shall publish it.
(4) A drug manufactured in a pilot or other small facility may be used to demonstrate the safety
and effectiveness of the drug and to obtain approval for the drug prior to manufacture of the
drug in a larger facility, unless the Secretary makes a determination that a full scale production
facility is necessary to ensure the safety or effectiveness of the drug.
(d)(1) If the Secretary finds, after due notice to the applicant in accordance with subsection (c)
and giving him an opportunity for a hearing, in accordance with said subsection, that—
(A) the investigations, reports of which are required to be submitted to the Secretary pursuant
to subsection (b), do not include adequate tests by all methods reasonably applicable to show
whether or not such drug is safe for use under the conditions prescribed, recommended, or
suggested in the proposed labeling thereof;
(B) the results of such tests show that such drug is unsafe for use under such conditions or do
not show that such drug is safe for use under such conditions;
(C) the methods used in, and the facilities and controls used for, the manufacture, processing,
and packing of such drug are inadequate to preserve its identity, strength, quality, and purity;
(D) upon the basis of the information submitted to him as part of the application, or upon the
basis of any other information before him with respect to such drug, he has insufficient
information to determine whether such drug is safe for use under such conditions;
(E) evaluated on the basis of the information submitted to him as part of the application and
any other information before him with respect to such drug, there is a lack of substantial
evidence that the drug will have the effect it purports or is represented to have under the
conditions of use prescribed, recommended, or suggested in the proposed labeling thereof;
(F) upon the basis of information submitted to the Secretary as part of the application or any
other information before the Secretary with respect to such drug, any use prescribed,
recommended, or suggested in labeling proposed for such drug will result in a residue of such
drug in excess of a tolerance found by the Secretary to be safe for such drug;
(G) the application failed to contain the patent information prescribed by subsection (b)(1);
(H) based on a fair evaluation of all material facts, such labeling is false or misleading in any
particular; or
(I) such drug induces cancer when ingested by man or animal or, after tests which are
appropriate for the evaluation of the safety of such drug, induces cancer in man or animal,
except that the foregoing provisions of this subparagraph shall not apply with respect to such
drug if the Secretary finds that, under the conditions of use specified in proposed labeling and
reasonably certain to be followed in practice (i) such drug will not adversely affect the animals
for which it is intended, and (ii) no residue of such drug will be found (by methods of
examination prescribed or approved by the Secretary by regulations, which regulations shall
not be subject to subsections (c), (d), and (h)), in any edible portion of such animals after
slaughter or in any food yielded by or derived from the living animals;
he shall issue an order refusing to approve the application. If, after such notice and opportunity
for hearing, the Secretary finds that subparagraphs (A) through (I) do not apply, he shall issue
an order approving the application.
(2) In determining whether such drug is safe for use under the conditions prescribed,
recommended, or suggested in the proposed labeling thereof, the Secretary shall consider,
among other relevant factors, (A) the probable consumption of such drug and of any
substance formed in or on food because of the use of such drug, (B) the cumulative effect on
man or animal of such drug, taking into account any chemically or pharmacologically related
substance, (C) safety factors which in the opinion of experts, qualified by scientific training and
experience to evaluate the safety of such drugs, are appropriate for the use of animal
experimentation data, and (D) whether the conditions of use prescribed, recommended, or
suggested in the proposed labeling are reasonably certain to be followed in practice. Any order
issued under this subsection refusing to approve an application shall state the findings upon
which it is based.
(3) As used in this section, the term "substantial evidence" means evidence consisting of one
or more adequate and well controlled investigations, such as—
(A) a study in a target species;
(B) a study in laboratory animals;
(C) any field investigation that may be required under this section and that meets the
requirements of subsection (b)(3) if a presubmission conference is requested by the applicant;
(D) a bioequivalence study; or
(E) an in vitro study; by experts qualified by scientific training and experience to evaluate the
effectiveness of the drug involved, on the basis of which it could fairly and reasonably be
concluded by such experts that the drug will have the effect it purports or is represented to
have under the conditions of use prescribed, recommended, or suggested in the labeling or
proposed labeling thereof.
(4) In a case in which an animal drug contains more than one active ingredient, or the labeling
of the drug prescribes, recommends, or suggests use of the drug in combination with one or
more other animal drugs, and the active ingredients or drugs intended for use in the
combination have previously been separately approved pursuant to an application submitted
under section 512(b)(1) 9 for particular uses and conditions of use for which they are intended
for use in the combination—
(A) the Secretary shall not issue an order under paragraph (1)(A), (1)(B), or (1)(D) refusing to
approve the application for such combination on human food safety grounds unless the
Secretary finds that the application fails to establish that—
(i) none of the active ingredients or drugs intended for use in the combination, respectively, at
the longest withdrawal time of any of the active ingredients or drugs in the combination,
respectively, exceeds its established tolerance; or
(ii) none of the active ingredients or drugs in the combination interferes with the methods of
analysis for another of the active ingredients or drugs in the combination, respectively;
(B) the Secretary shall not issue an order under paragraph (1)(A), (1)(B), or (1)(D) refusing to
approve the application for such combination on target animal safety grounds unless the
Secretary finds that—
(i)(I) there is a substantiated scientific issue, specific to one or more of the active ingredients or
animal drugs in the combination, that cannot adequately be evaluated based on information
contained in the application for the combination (including any investigations, studies, or tests
for which the applicant has a right of reference or use from the person by or for whom the
investigations, studies, or tests were conducted); or
(II) there is a scientific issue raised by target animal observations contained in studies
submitted to the Secretary as part of the application; and
(ii) based on the Secretary’s evaluation of the information contained in the application with
respect to the issues identified in clauses (i) (I) and (II), paragraph (1) (A), (B), or (D) apply;
(C) except in the case of a combination that contains a nontopical antibacterial ingredient or
animal drug, the Secretary shall not issue an order under paragraph (1)(E) refusing to approve
an application for a combination animal drug intended for use other than in animal feed or
drinking water unless the Secretary finds that the application fails to demonstrate that—
(i) there is substantial evidence that any active ingredient or animal drug intended only for the
same use as another active ingredient or animal drug in the combination makes a contribution
to labeled effectiveness;
(ii) each active ingredient or animal drug intended for at least one use that is different from all
other active ingredients or animal drugs used in the combination provides appropriate
concurrent use for the intended target population; or
(iii) where based on scientific information the Secretary has reason to believe the active
ingredients or animal drugs may be physically incompatible or have disparate dosing regimens,
such active ingredients or animal drugs are physically compatible or do not have disparate
dosing regimens; and
(D) the Secretary shall not issue an order under paragraph (1)(E) refusing to approve an
application for a combination animal drug intended for use in animal feed or drinking water
unless the Secretary finds that the application fails to demonstrate that—
(i) there is substantial evidence that any active ingredient or animal drug intended only for the
same use as another active ingredient or animal drug in the combination makes a contribution
to the labeled effectiveness;
(ii) each of the active ingredients or animal drugs intended for at least one use that is different
from all other active ingredients or animal drugs used in the combination provides appropriate
concurrent use for the intended target population;
(iii) where a combination contains more than one nontopical antibacterial ingredient or animal
drug, there is substantial evidence that each of the nontopical antibacterial ingredients or
animal drugs makes a contribution to the labeled effectiveness, except that for purposes of this
clause, antibacterial ingredient or animal drug does not include the ionophore or arsenical
classes of animal drugs; or
(iv) where based on scientific information the Secretary has reason to believe the active
ingredients or animal drugs intended for use in drinking water may be physically incompatible,
such active ingredients or animal drugs intended for use in drinking water are physically
compatible.
(5) 10 In reviewing an application that proposes a change to add an intended use for a minor
use or a minor species to an approved new animal drug application, the Secretary shall
reevaluate only the relevant information in the approved application to determine whether the
application for the minor use or minor species can be approved. A decision to approve the
application for the minor use or minor species is not, implicitly or explicitly, a reaffirmation of
the approval of the original application.
(e)(1) The Secretary shall, after due notice and opportunity for hearing to the applicant, issue
an order withdrawing approval of an application filed pursuant to subsection (b) with respect to
any new animal drug if the Secretary finds—
(A) that experience or scientific data show that such drug is unsafe for use under the
conditions of use upon the basis of which the application was approved or the condition of use
authorized under subsection (a)(4)(A);
(B) that new evidence not contained in such application or not available to the Secretary until
after such application was approved, or tests by new methods, or tests by methods not
deemed reasonably applicable when such application was approved, evaluated together with
the evidence available to the Secretary when the application was approved, shows that such
drug is not shown to be safe for use under the conditions of use upon the basis of which the
application was approved or that subparagraph (I) of paragraph (1) of subsection (d) applies to
such drug;
(C) on the basis of new information before him with respect to such drug, evaluated together
with the evidence available to him when the application was approved, that there is a lack of
substantial evidence that such drug will have the effect it purports or is represented to have
under the conditions of use prescribed, recommended, or suggested in the labeling thereof;
(D) the patent information prescribed by subsection (c)(3) was not filed within 30 days after the
receipt of written notice from the Secretary specifying the failure to file such information;
(E) that the application contains any untrue statement of a material fact; or
(F) that the applicant has made any changes from the standpoint of safety or effectiveness
beyond the variations provided for in the application unless he has supplemented the
application by filing with the Secretary adequate information respecting all such changes and
unless there is in effect an approval of the supplemental application. The supplemental
application shall be treated in the same manner as the original application.
If the Secretary (or in his absence the officer acting as Secretary) finds that there is an
imminent hazard to the health of man or of the animals for which such drug is intended, he
may suspend the approval of such application immediately, and give the applicant prompt
notice of his action and afford the applicant the opportunity for an expedited hearing under this
subsection; but the authority conferred by this sentence to suspend the approval of an
application shall not be delegated.
(2) The Secretary may also, after due notice and opportunity for hearing to the applicant, issue
an order withdrawing the approval of an application with respect to any new animal drug under
this section if the Secretary finds—
(A) that the applicant has failed to establish a system for maintaining required records, or has
repeatedly or deliberately failed to maintain such records or to make required reports in
accordance with a regulation or order under subsection (l), or the applicant has refused to
permit access to, or copying or verification of, such records as required by paragraph (2) of
such subsection;
(B) that on the basis of new information before him, evaluated together with the evidence
before him when the application was approved, the methods used in, or the facilities and
controls used for, the manufacture, processing, and packing of such drug are inadequate to
assure and preserve its identity, strength, quality, and purity and were not made adequate
within a reasonable time after receipt of written notice from the Secretary specifying the matter
complained of; or
(C) that on the basis of new information before him, evaluated together with the evidence
before him when the application was approved, the labeling of such drug, based on a fair
evaluation of all material facts, is false or misleading in any particular and was not corrected
within a reasonable time after receipt of written notice from the Secretary specifying the matter
complained of.
(3) Any order under this subsection shall state the findings upon which it is based.
(f) Whenever the Secretary finds that the facts so require, he shall revoke any previous order
under subsection (d), (e), or (m), or section 571 (c), (d), or (e) refusing, withdrawing, or
suspending approval of an application and shall approve such application or reinstate such
approval, as may be appropriate.
(g) Orders of the Secretary issued under this section, or section 571(other than orders issuing,
amending, or repealing regulations) shall be served (1) in person by any officer or employee of
the department designated by the Secretary or (2) by mailing the order by registered mail or by
certified mail addressed to the applicant or respondent at his last known address in the records
of the Secretary.
(h) An appeal may be taken by the applicant from an order of the Secretary refusing or
withdrawing approval of an application filed under subsection (b) or (m) of this section. The
provisions of subsection (h) of section 505 of this Act shall govern any such appeal.
(i) When a new animal drug application filed pursuant to subsection (b) or section 571 is
approved, the Secretary shall by notice, which upon publication shall be effective as a
regulation, publish in the Federal Register the name and address of the applicant and the
conditions and indications of use of the new animal drug covered by such application,
including any tolerance and withdrawal period or other use restrictions and, if such new animal
drug is intended for use in animal feed, appropriate purposes and conditions of use (including
special labeling requirements and any requirement that an animal feed bearing or containing
the new animal drug be limited to use under the professional supervision of a licensed
veterinarian) applicable to any animal feed for use in which such drug is approved, and such
other information, upon the basis of which such application was approved, as the Secretary
deems necessary to assure the safe and effective use of such drug. Upon withdrawal of
approval of such new animal drug application or upon its suspension or upon failure to renew a
conditional approval under section 571, the Secretary shall forthwith revoke or suspend, as the
case may be, the regulation published pursuant to this subsection (i) 11 insofar as it is based
on the approval of such application.
(j) To the extent consistent with the public health, the Secretary shall promulgate regulations
for exempting from the operation of this section new animal drugs, and animal feeds bearing or
containing new animal drugs, intended solely for investigational use by experts qualified by
scientific training and experience to investigate the safety and effectiveness of animal drugs.
Such regulations may, in the discretion of the Secretary, among other conditions relating to the
protection of the public health, provide for conditioning such exemption upon the establishment
and maintenance of such records, and the making of such reports to the Secretary, by the
manufacturer or the sponsor of the investigation of such article, of data (including but not
limited to analytical reports by investigators) obtained as a result of such investigational use of
such article, as the Secretary finds will enable him to evaluate the safety and effectiveness of
such article in the event of the filing of an application pursuant to this section. Such regulations,
among other things, shall set forth the conditions (if any) upon which animals treated with such
articles, and any products of such animals (before or after slaughter), may be marketed for
food use.
(k) While approval of an application for a new animal drug is effective, a food shall not, by
reason of bearing or containing such drug or any substance formed in or on the food because
of its use in accordance with such application (including the conditions and indications of use
prescribed pursuant to subsection (i)), be considered adulterated within the meaning of clause
(1) of section 402(a).
(l)(1) In the case of any new animal drug for which an approval of an application filed pursuant
to ubsection (b) or section 571 is in effect, the applicant shall establish and maintain such
records, and make such reports to the Secretary, of data relating to experience, including
experience with uses authorized under subsection (a)(4)(A), and other data or information,
received or otherwise obtained by such applicant with respect to such drug, or with respect to
animal feeds bearing or containing such drug, as the Secretary may by general regulation, or
by order with respect to such application, prescribe on the basis of a finding that such records
and reports are necessary in order to enable the Secretary to determine, or facilitate a
determination, whether there is or may be ground for invoking subsection (e) or subsection
(m)(4) of this section. Such regulation or order shall provide, where the Secretary deems it to
be appropriate, for the examination, upon request, by the persons to whom such regulation or
order is applicable, of similar information received or otherwise obtained by the Secretary.
(2) Every person required under this subsection to maintain records, and every person in
charge or custody thereof, shall, upon request of an officer or employee designated by the
Secretary, permit such officer or employee at all reasonable times to have access to and copy
and verify such records.
(m)(1) Any person may file with the Secretary an application for a license to manufacture
animal feeds bearing or containing new animal drugs. Such person shall submit to the
Secretary as part of the application (A) a full statement of the business name and address of
the specific facility at which the manufacturing is to take place and the facility’s registration
number, (B) the name and signature of the responsible individual or individuals for that facility,
(C) a certification that the animal feeds bearing or containing new animal drugs are
manufactured and labeled in accordance with the applicable regulations published pursuant to
subsection (i) or for indexed new animal drugs in accordance with the index listing published
pursuant to section 572(e)(2) and the labeling requirements set forth in section 572(h), and (D)
a certification that the methods used in, and the facilities and controls used for, manufacturing,
processing, packaging, and holding such animal feeds are in conformity with current good
manufacturing practice as described in section 501(a)(2)(B).
(2) Within 90 days after the filing of an application pursuant to paragraph (1), or such additional
period as may be agreed upon by the Secretary and the applicant, the Secretary shall (A)
issue an order approving the application if the Secretary then finds that none of the grounds for
denying approval specified in paragraph (3) applies, or (B) give the applicant notice of an
opportunity for a hearing before the Secretary under paragraph (3) on the question whether
such application is approvable. The procedure governing such a hearing shall be the
procedure set forth in the last two sentences of subsection (c)(1).
(3) If the Secretary, after due notice to the applicant in accordance with paragraph (2) and
giving the applicant an opportunity for a hearing in accordance with such paragraph, finds, on
the basis of information submitted to the Secretary as part of the application, on the basis of a
preapproval inspection, or on the basis of any other information before the Secretary—
(A) that the application is incomplete, false, or misleading in any particular;
(B) that the methods used in, and the facilities and controls used for, the manufacture,
processing, and packing of such animal feed are inadequate to preserve the identity, strength,
quality, and purity of the new animal drug therein; or
(C) that the facility manufactures animal feeds bearing or containing new animal drugs in a
manner that does not accord with the specifications for manufacture or labels animal feeds
bearing or containing new animal drugs in a manner that does not accord with the conditions
or indications of use that are published pursuant to subsection (i) or an index listing pursuant to
section 572(e),
the Secretary shall issue an order refusing to approve the application. If, after such notice and
opportunity for hearing, the Secretary finds that subparagraphs (A) through (C) do not apply,
the Secretary shall issue an order approving the application. An order under this subsection
approving an application for a license to manufacture animal feeds bearing or containing new
animal drugs shall permit a facility to manufacture only those animal feeds bearing or
containing new animal drugs for which there are in effect regulations pursuant to subsection (i)
or an index listing pursuant to section 572(e) relating to the use of such drugs in or on such
animal feed.
(4)(A) The Secretary shall, after due notice and opportunity for hearing to the applicant, revoke
a license to manufacture animal feeds bearing or containing new animal drugs under this
subsection if the Secretary finds—
(i) that the application for such license contains any untrue statement of a material fact; or
(ii) that the applicant has made changes that would cause the application to contain any untrue
statements of material fact or that would affect the safety or effectiveness of the animal feeds
manufactured at the facility unless the applicant has supplemented the application by filing
with the Secretary adequate information respecting all such changes and unless there is in
effect an approval of the supplemental application.
If the Secretary (or in the Secretary’s absence the officer acting as the Secretary) finds that
there is an imminent hazard to the health of humans or of the animals for which such animal
feed is intended, the Secretary may suspend the license immediately, and give the applicant
prompt notice of the action and afford the applicant the opportunity for an expedited hearing
under this subsection; but the authority conferred by this sentence shall not be delegated.
(B) The Secretary may also, after due notice and opportunity for hearing to the applicant,
revoke a license to manufacture animal feed under this subsection if the Secretary finds—
(i) that the applicant has failed to establish a system for maintaining required records, or has
repeatedly or deliberately failed to maintain such records or to make required reports in
accordance with a regulation or order under paragraph (5)(A) of this subsection or section
504(a)(3)(A), or the applicant has refused to permit access to, or copying or verification of,
such records as required by subparagraph (B) of such paragraph or section 504(a)(3)(B);
(ii) that on the basis of new information before the Secretary, evaluated together with the
evidence before the Secretary when such license was issued, the methods used in, or the
facilities and controls used for, the manufacture, processing, packing, and holding of such
animal feed are inadequate to assure and preserve the identity, strength, quality, and purity of
the new animal drug therein, and were not made adequate within a reasonable time after
receipt of written notice from the Secretary, specifying the matter complained of;
(iii) that on the basis of new information before the Secretary, evaluated together with the
evidence before the Secretary when such license was issued, the labeling of any animal feeds,
based on a fair evaluation of all material facts, is false or misleading in any particular and was
not corrected within a reasonable time after receipt of written notice from the Secretary
specifying the matter complained of; or
(iv) that on the basis of new information before the Secretary, evaluated together with the
evidence before the Secretary when such license was issued, the facility has manufactured,
processed, packed, or held animal feed bearing or containing a new animal drug adulterated
under section 501(a)(6) and the facility did not discontinue the manufacture, processing,
packing, or holding of such animal feed within a reasonable time after receipt of written notice
from the Secretary specifying the matter complained of.
(C) The Secretary may also revoke a license to manufacture animal feeds under this
subsection if an applicant gives notice to the Secretary of intention to discontinue the
manufacture of all animal feed covered under this subsection and waives an opportunity for a
hearing on the matter.
(D) Any order under this paragraph shall state the findings upon which it is based.
(5) When a license to manufacture animal feeds bearing or containing new animal drugs has
been issued—
(A) the applicant shall establish and maintain such records, and make such reports to the
Secretary, or (at the option of the Secretary) to the appropriate person or persons holding an
approved application filed under subsection (b), as the Secretary may by general regulation, or
by order with respect to such application, prescribe on the basis of a finding that such records
and reports are necessary in order to enable the Secretary to determine, or facilitate a
determination, whether there is or may be ground for invoking subsection (e) or paragraph (4);
and
(B) every person required under this subsection to maintain records, and every person in
charge or custody thereof, shall, upon request of an officer or employee designated by the
Secretary, permit such officer or employee at all reasonable times to have access to and copy
and verify such records.
(6) To the extent consistent with the public health, the Secretary may promulgate regulations
for exempting from the operation of this subsection facilities that manufacture, process, pack,
or hold animal feeds bearing or containing new animal drugs.
(n)(1) An abbreviated application for a new animal drug shall contain—
(A)(i) except as provided in clause (ii), information to show that the conditions of use or similar
limitations (whether in the labeling or published pursuant to subsection (i)) prescribed,
recommended, or suggested in the labeling proposed for the new animal drug have been
previously approved for a new animal drug listed under paragraph (4) (hereinafter in this
subsection referred to as an "approved new animal drug"), and
(ii) information to show that the withdrawal period at which residues of the new animal drug will
be consistent with the tolerances established for the approved new animal drug is the same as
the withdrawal period previously established for the approved new animal drug or, if the
withdrawal period is proposed to be different, information showing that the residues of the new
animal drug at the proposed different withdrawal period will be consistent with the tolerances
established for the approved new animal drug;
(B)(i) information to show that the active ingredients of the new animal drug are the same as
those of the approved new animal drug, and
(ii) if the approved new animal drug has more than one active ingredient, and if one of the
active ingredients of the new animal drug is different from one of the active ingredients of the
approved new animal drug and the application is filed pursuant to the approval of a petition
filed under paragraph (3)—
(I) information to show that the other active ingredients of the new animal drug are the same as
the active ingredients of the approved new animal drug,
(II) information to show either that the different active ingredient is an active ingredient of
another approved new animal drug or of an animal drug which does not meet the requirements
of section 201(v), and
(III) such other information respecting the different active ingredients as the Secretary may
require;
(C)(i) if the approved new animal drug is permitted to be used with one or more animal drugs in
animal feed, information to show that the proposed uses of the new animal drug with other
animal drugs in animal feed are the same as the uses of the approved new animal drug, and
(ii) if the approved new animal drug is permitted to be used with one or more other animal
drugs in animal feed, and one of the other animal drugs proposed for use with the new animal
drug in animal feed is different from one of the other animal drugs permitted to be used in
animal feed with the approved new animal drug, and the application is filed pursuant to the
approval of a petition filed under paragraph (3)—
(I) information to show either that the different animal drug proposed for use with the approved
new animal drug in animal feed is an approved new animal drug permitted to be used in animal
feed or does not meet the requirements of section 201(v) when used with another animal drug
in animal feed,
(II) information to show that other animal drugs proposed for use with the new animal drug in
animal feed are the same as the other animal drugs permitted to be used with the approved
new animal drug, and
(III) such other information respecting the different animal drug or combination with respect to
which the petition was filed as the Secretary may require,
(D) information to show that the route of administration, the dosage form, and the strength of
the new animal drug are the same as those of the approved new animal drug or, if the route of
administration, the dosage form, or the strength of the new animal drug is different and the
application is filed pursuant to the approval of a petition filed under paragraph (3), such
information respecting the route of administration, dosage form, or strength with respect to
which the petition was filed as the Secretary may require;
(E) information to show that the new animal drug is bioequivalent to the approved new animal
drug, except that if the application is filed pursuant to the approval of a petition filed under
paragraph (3) for the purposes described in subparagraph (B) or (C), information to show that
the active ingredients of the new animal drug are of the same pharmacological or therapeutic
class as the pharmacological or therapeutic class of the approved new animal drug and that
the new animal drug can be expected to have the same therapeutic effect as the approved
new animal drug when used in accordance with the labeling;
(F) information to show that the labeling proposed for the new animal drug is the same as the
labeling approved for the approved new animal drug except for changes required because of
differences approved under a petition filed under paragraph (3), because of a different
withdrawal period, or because the new animal drug and the approved new animal drug are
produced or distributed by different manufacturers;
(G) the items specified in clauses (B) through (F) of subsection (b)(1);
(H) a certification, in the opinion of the applicant and to the best of his knowledge, with respect
to each patent which claims the approved new animal drug or which claims a use for such
approved new animal drug for which the applicant is seeking approval under this subsection
and for which information is required to be filed under subsection (b)(1) or (c)(3)—
(i) that such patent information has not been filed,
(ii) that such patent has expired,
(iii) of the date on which such patent will expire, or
(iv) that such patent is invalid or will not be infringed by the manufacture, use, or sale of the
new animal drug for which the application is filed; and
(I) if with respect to the approved new animal drug information was filed under subsection (b)(1)
or (c)(3) for a method of use patent which does not claim a use for which the applicant is
seeking approval of an application under subsection (c)(2), a statement that the method of use
patent does not claim such a use.
The Secretary may not require that an abbreviated application contain information in addition
to that required by subparagraphs (A) through (I).
(2)(A) An applicant who makes a certification described in paragraph (1)(G)(iv) shall include in
the application a statement that the applicant will give the notice required by subparagraph (B)
to—
(i) each owner of the patent which is the subject of the certification or the representative of
such owner designated to receive such notice, and
(ii) the holder of the approved application under subsection (c)(1) for the drug which is claimed
by the patent or a use of which is claimed by the patent or the representative of such holder
designated to receive such notice.
(B) The notice referred to in subparagraph (A) shall state that an application, which contains
data from bioequivalence studies, has been filed under this subsection for the drug with
respect to which the certification is made to obtain approval to engage in the commercial
manufacture, use, or sale of such drug before the expiration of the patent referred to in the
certification. Such notice shall include a detailed statement of the factual and legal basis of the
applicant’s opinion that the patent is not valid or will not be infringed.
(C) If an application is amended to include a certification described in paragraph (1)(G)(iv), the
notice required by subparagraph (B) shall be given when the amended application is filed.
(3) If a person wants to submit an abbreviated application for a new animal drug—
(A) whose active ingredients, route of administration, dosage form, or strength differ from that
of an approved new animal drug, or
(B) whose use with other animal drugs in animal feed differs from that of an approved new
animal drug, such person shall submit a petition to the Secretary seeking permission to file
such an application. The Secretary shall approve a petition for a new animal drug unless the
Secretary finds that—
(C) investigations must be conducted to show the safety and effectiveness, in animals to be
treated with the drug, of the active ingredients, route of administration, dosage form, strength,
or use with other animal drugs in animal feed which differ from the approved new animal drug,
or
(D) investigations must be conducted to show the safety for human consumption of any
residues in food resulting from the proposed active ingredients, route of administration, dosage
form, strength, or use with other animal drugs in animal feed for the new animal drug which is
different from the active ingredients, route of administration, dosage form, strength, or use with
other animal drugs in animal feed of the approved new animal drug.
The Secretary shall approve or disapprove a petition submitted under this paragraph within 90
days of the date the petition is submitted.
(4)(A)(i) Within 60 days of the date of the enactment of this subsection 1, the Secretary shall
publish and make available to the public a list in alphabetical order of the official and
proprietary name of each new animal drug which has been approved for safety and
effectiveness before the date of the enactment of this subsection.
(ii) Every 30 days after the publication of the first list under clause (i) the Secretary shall revise
the list to include each new animal drug which has been approved for safety and effectiveness
under subsection (c) during the 30 day period.
(iii) When patent information submitted under subsection (b)(1) or (c)(3) respecting a new
animal drug included on the list is to be published by the Secretary, the Secretary shall, in
revisions made under clause (ii), include such information for such drug.
(B) A new animal drug approved for safety and effectiveness before the date of the enactment
of this subsection or approved for safety and effectiveness under subsection (c) shall, for
purposes of this subsection, be considered to have been published under subparagraph (A) on
the date of its approval or the date of enactment, whichever is later.
(C) If the approval of a new animal drug was withdrawn or suspended under subsection
(c)(2)(G) or for grounds described in subsection (e) or if the Secretary determines that a drug
has been withdrawn from sale for safety or effectiveness reasons, it may not be published in
the list under subparagraph (A) or, if the withdrawal or suspension occurred after its
publication in such list, it shall be immediately removed from such list—
(i) for the same period as the withdrawal or suspension under subsection (c)(2)(G) or (e), or
(ii) if the listed drug has been withdrawn from sale, for the period of withdrawal from sale or, if
earlier, the period ending on the date the Secretary determines that the withdrawal from sale is
not for safety or effectiveness reasons.
A notice of the removal shall be published in the Federal Register.
(5) If an application contains the information required by clauses (A), (G), and (H) of
subsection (b)(1) and such information—
(A) is relied on by the applicant for the approval of the application, and
(B) is not information derived either from investigations, studies, or tests conducted by or for
the applicant or for which the applicant had obtained a right of reference or use from the
person by or for whom the investigations, studies, or tests were conducted, such application
shall be considered to be an application filed under subsection (b)(2).
(o) For purposes of this section, the term "patent" means a patent issued by the United States
Patent and Trademark Office.
(p)(1) Safety and effectiveness data and information which has been submitted in an
application filed under subsection (b)(1) or section 571(a) for a drug and which has not
previously been disclosed to the public shall be made available to the public, upon request,
unless extraordinary circumstances are shown—
(A) if no work is being or will be undertaken to have the application approved,
(B) if the Secretary has determined that the application is not approvable and all legal appeals
have been exhausted,
(C) if approval of the application under subsection (c) is withdrawn and all legal appeals have
been exhausted,
(D) if the Secretary has determined that such drug is not a new drug, or
(E) upon the effective date of the approval of the first application filed under subsection (b)(2)
which refers to such drug or upon the date upon which the approval of an application filed
under subsection (b)(2) which refers to such drug could be made effective if such an
application had been filed.
(2) Any request for data and information pursuant to paragraph (1) shall include a verified
statement by the person making the request that any data or information received under such
paragraph shall not be disclosed by such person to any other person—
(A) for the purpose of, or as part of a plan, scheme, or device for, obtaining the right to make,
use, or market, or making, using, or marketing, outside the United States, the drug identified in
the application filed under subsection (b)(1) or section 571(a), and
(B) without obtaining from any person to whom the data and information are disclosed an
identical verified statement, a copy of which is to be provided by such person to the Secretary,
which meets the requirements of this paragraph.
Footnotes: Section 512
1. Section 511 was repealed by section 701(a) of Public Law 91–513.
2. Section 512 was added by Public Law 90–399, which was enacted July 13, 1968. Section
108 of such Public Law concerned the effective date and applicability of the amendment, and
is included in the appendix to this compilation.
3. Separate indentation of paragraph (1) is so in law. See section 102(b)(5)(I) of Public Law
108–282.
4. So in law. Probably should be "clause (iii)(III)".
5. The reference to "this paragraph" is a reference to paragraph (2) of subsection (c).
Paragraph (2) was added by title I of Public Law 100–670, which was enacted November 16,
1988.
6. The language within parentheses appears so as to reflect the probable intent of the
Congress. Section 102(b)(2) of Public Law 108–282 provides for amendments to the
parenentical language, and states that "Section 512(c)(2)(F) (ii), (iii), and (v) of the Federal
Food, Drug, and Cosmetic Act is amended by". The probable intent of the Congress was to
provide that "Clauses (ii), (iii), and (v) of section 512(c)(2)(F) of the Federal Food, Drug, and
Cosmetic Act are each amended by".
7. The reference to "this paragraph" is a reference to paragraph (2) of subsection (c).
Paragraph
(2) was added by title I of Public Law 100–670, which was enacted November 16, 1988.
8. The sentence was added by title I of Public Law 100–670, which was enacted November 16,
1988.
9. 1 So in law. See section 102(b)(5)(K) of Public Law 108-282. Probably should be
"subsection (b)(1)".
10. Identation is so in law. See section 102(b)(3) of Public Law 108-282.
11. So in law. Probably should be "this subsection".
CHAPTER V--DRUGS AND DEVICES SUBCHAPTER A--DRUGS AND DEVICES
CLASSIFICATION OF DEVICES INTENDED FOR HUMAN USE
SEC. 513. [21 U.S.C. 360c ] (a) Device Classes
(1) There are established the following classes of devices intended for human use:
(A) CLASS I, GENERAL CONTROLS.—
(i) A device for which the controls authorized by or under section 501, 502, 510, 516, 518, 519,
or 520 or any combination of such sections are sufficient to provide reasonable assurance of
the safety and effectiveness of the device.
(ii) A device for which insufficient information exists to determine that the controls referred to in
clause (i) are sufficient to provide reasonable assurance of the safety and effectiveness of the
device or to establish special controls to provide such assurance, but because it—
(I) is not purported or represented to be for a use in supporting or sustaining human life or for a
use which is of substantial importance in preventing impairment of human health, and
(II) does not present a potential unreasonable risk of illness or injury,
is to be regulated by the controls referred to in clause (i).
(B) CLASS II, SPECIAL CONTROLS.—A device which cannot be classified as a class I device
because the general controls by themselves are insufficient to provide reasonable assurance
of the safety and effectiveness of the device, and for which there is sufficient information to
establish special controls to provide such assurance, including the promulgation of
performance standards, postmarket surveillance, patient registries, development and
dissemination of guidelines (including guidelines for the submission of clinical data in
premarket notification submissions in accordance with section 510(k)), recommendations, and
other appropriate actions as the Secretary deems necessary to provide such assurance. For a
device that is purported or represented to be for a use in supporting or sustaining human life,
the Secretary shall examine and identify the special controls, if any, that are necessary to
provide adequate assurance of safety and effectiveness and describe how such controls
provide such assurance.
(C) CLASS III, PREMARKET APPROVAL.—A device which because—
(i) it (I) cannot be classified as a class I device because insufficient information exists to
determine that the application of general controls are sufficient to provide reasonable
assurance of the safety and effectiveness of the device, and (II) cannot be classified as a class
II device because insufficient information exists to determine that the special controls
described in subparagraph (B) would provide reasonable assurance of its safety and
effectiveness, and
(ii)(I) is purported or represented to be for a use in supporting or sustaining human life or for a
use which is of substantial importance in preventing impairment of human health, or
(II) presents a potential unreasonable risk of illness or injury,
is to be subject, in accordance with section 515, to Premarket approval to provide reasonable
assurance of its safety and effectiveness.
If there is not sufficient information to establish a performance standard for a device to provide
reasonable assurance of its safety and effectiveness, the Secretary may conduct such
activities as may be necessary to develop or obtain such information.
(2) For purposes of this section and sections 514 and 515, the safety and effectiveness of a
device are to be determined—
(A) with respect to the persons for whose use the device is represented or intended,
(B) with respect to the conditions of use prescribed, recommended, or suggested in the
labeling of the device, and
(C) weighing any probable benefit to health from the use of the device against any probable
risk of injury or illness from such use.
(3)(A) Except as authorized by subparagraph (B), the effectiveness of a device is, for purposes
of this section and sections 514 and 515, to be determined, in accordance with regulations
promulgated by the Secretary, on the basis of well-controlled investigations, including 1 or
more clinical investigations where appropriate, by experts qualified by training and experience
to evaluate the effectiveness of the device, from which investigations it can fairly and
responsibly be concluded by qualified experts that the device will have the effect it purports or
is represented to have under the conditions of use prescribed, recommended, or suggested in
the labeling of the device.
(B) If the Secretary determines that there exists valid scientific evidence (other than evidence
derived from investigations described in subparagraph (A))—
(i) which is sufficient to determine the effectiveness of a device, and
(ii) from which it can fairly and responsibly be concluded by qualified experts that the device
will have the effect it purports or is represented to have under the conditions of use prescribed,
recommended, or suggested in the labeling of the device, then, for purposes of this section
and sections 514 and 515, the Secretary may authorize the effectiveness of the device to be
determined on the basis of such evidence.
(C) In making a determination of a reasonable assurance of the effectiveness of a device for
which an application under section 515 has been submitted, the Secretary shall consider
whether the extent of data that otherwise would be required for approval of the application with
respect to effectiveness can be reduced through reliance on postmarket controls.
(D)(i) The Secretary, upon the written request of any person intending to submit an application
under section 515, shall meet with such person to determine the type of valid scientific
evidence (within the meaning of subparagraphs (A) and (B)) that will be necessary to
demonstrate for purposes of approval of an application the effectiveness of a device for the
conditions of use proposed by such person. The written request shall include a detailed
description of the device, a detailed description of the proposed conditions of use of the device,
a proposed plan for determining whether there is a reasonable assurance of effectiveness,
and, if available, information regarding the expected performance from the device. Within 30
days after such meeting, the Secretary shall specify in writing the type of valid scientific
evidence that will provide a reasonable assurance that a device is effective under the
conditions of use proposed by such person.
(ii) Any clinical data, including one or more well-controlled investigations, specified in writing by
the Secretary for demonstrating a reasonable assurance of device effectiveness shall be
specified as result of a determination by the Secretary that such data are necessary to
establish device effectiveness. The Secretary shall consider, in consultation with the applicant,
the least burdensome appropriate means of evaluating device effectiveness that would have a
reasonable likelihood of resulting in approval.
(iii) The determination of the Secretary with respect to the specification of valid scientific
evidence under clauses (i) and (ii) shall be binding upon the Secretary, unless such
determination by the Secretary could be contrary to the public health.
(b) Classification; Classification Panels
(1) For purposes of—
(A) determining which devices intended for human use should be subject to the requirements
of general controls, performance standards, or premarket approval, and
(B) providing notice to the manufacturers and importers of such devices to enable them to
prepare for the application of such requirements to devices manufactured or imported by them,
the Secretary shall classify all such devices (other than devices classified by subsection (f))
into the classes established by subsection (a). For the purpose of securing recommendations
with respect to the classification of devices, the Secretary shall establish panels of experts or
use panels of experts established before the date of the enactment of this section, or both.
Section 14 of the Federal Advisory Committee Act shall not apply to the duration of a panel
established under this paragraph.
(2) The Secretary shall appoint to each panel established under paragraph (1) persons who
are qualified by training and experience to evaluate the safety and effectiveness of the devices
to be referred to the panel and who, to the extent feasible, possess skill in the use of, or
experience in the development, manufacture, or utilization of, such devices. The Secretary
shall make appointments to each panel so that each panel shall consist of members with
adequately diversified expertise in such fields as clinical and administrative medicine,
engineering, biological and physical sciences, and other related professions. In addition, each
panel shall include as nonvoting members a representative of consumer interests and a
representative of interests of the device manufacturing industry. Scientific, trade, and
consumer organizations shall be afforded an opportunity to nominate individuals for
appointment to the panels. No individual who is in the regular full-time employ of the United
States and engaged in the administration of this Act may be a member of any panel. The
Secretary shall designate one of the members of each panel to serve as chairman thereof.
(3) Panel members (other than officers or employees of the United States), while attending
meetings or conferences of a panel or otherwise engaged in its business, shall be entitled to
receive compensation at rates to be fixed by the Secretary, but not at rates exceeding the daily
equivalent of the rate in effect for grade GS–18 of the General Schedule 1 , for each day so
engaged, including travel time; and while so serving away from their homes or regular places
of business each member may be allowed travel expenses (including per diem in lieu of
subsistence) as authorized by section 5703 of title 5, United States Code, for persons in the
Government service employed intermittently.
(4) The Secretary shall furnish each panel with adequate clerical and other necessary
assistance.
(5) Classification panels covering each type of device shall be scheduled to meet at such times
as may be appropriate for the Secretary to meet applicable statutory deadlines.
(6)(A) Any person whose device is specifically the subject of review by a classification panel
shall have—
(i) the same access to data and information submitted to a classification panel (except for data
and information that are not available for public disclosure under section 552 of title 5, United
States Code) as the Secretary;
(ii) the opportunity to submit, for review by a classification panel, information that is based on
the data or information provided in the application submitted under section 515 by the person,
which information shall be submitted to the Secretary for prompt transmittal to the
classification panel; and
(iii) the same opportunity as the Secretary to participate in meetings of the panel.
(B) Any meetings of a classification panel shall provide adequate time for initial presentations
and for response to any differing views by persons whose devices are specifically the subject
of a classification panel review, and shall encourage free and open participation by all
interested persons.
(7) After receiving from a classification panel the conclusions and recommendations of the
panel on a matter that the panel has reviewed, the Secretary shall review the conclusions and
recommendations, shall make a final decision on the matter in accordance with section
515(d)(2), and shall notify the affected persons of the decision in writing and, if the decision
differs from the conclusions and recommendations of the panel, shall include the reasons for
the difference.
(8) A classification panel under this subsection shall not be subject to the annual chartering
and annual report requirements of the Federal Advisory Committee Act.
(c) Classification Panel Organization and Operation
(1) The Secretary shall organize the panels according to the various fields of clinical medicine
and fundamental sciences in which devices intended for human use are used. The Secretary
shall refer a device to be classified under this section to an appropriate panel established or
authorized to be used under subsection (b) for its review and for its recommendation
respecting the classification of the device. The Secretary shall by regulation prescribe the
procedure to be followed by the panels in making their reviews and recommendations. In
making their reviews of devices, the panels, to the maximum extent practicable, shall provide
an opportunity for interested persons to submit data and views on the classification of the
devices.
(2)(A) Upon completion of a panel’s review of a device referred to it under paragraph (1), the
panel shall, subject to subparagraphs (B) and (C), submit to the Secretary its recommendation
for the classification of the device. Any such recommendation shall (i) contain (I) a summary of
the reasons for the recommendation, (II) a summary of the data upon which the
recommendation is based, and (III) an identification of the risks to health (if any) presented by
the device with respect to which the recommendation is made, and (ii) to the extent practicable,
include a recommendation for the assignment of a priority for the application of the
requirements of section 514 or 515 to a device recommended to be classified in class II or
class III.
(B) A recommendation of a panel for the classification of a device in class I shall include a
recommendation as to whether the device should be exempted from the requirements of
section 510, 519, or 520(f).
(C) In the case of a device which has been referred under paragraph (1) to a panel, and
which—
(i) is intended to be implanted in the human body or is purported or represented to be for a use
in supporting or sustaining human life, and
(ii)(I) has been introduced or delivered for introduction into interstate commerce for commercial
distribution before the date of enactment of this section, or
(II) is within a type of device which was so introduced or delivered before such date and is
substantially equivalent to another device within that type,
such panel shall recommend to the Secretary that the device be classified in class III unless
the panel determines that classification of the device in such class is not necessary to provide
reasonable assurance of its safety and effectiveness. If a panel does not recommend that such
a device be classified in class III, it shall in its recommendation to the Secretary for the
classification of the device set forth the reasons for not recommending classification of the
device in such class.
(3) The panels shall submit to the Secretary within one year of the date funds are first
appropriated for the implementation of this section their recommendations respecting all
devices of a type introduced or delivered for introduction into interstate commerce for
commercial distribution before the date of the enactment of this section.
(d) Classification
(1) Upon receipt of a recommendation from a panel respecting a device, the Secretary shall
publish in the Federal Register the panel’s recommendation and a proposed regulation
classifying such device and shall provide interested persons an opportunity to submit
comments on such recommendation and the proposed regulation. After reviewing such
comments, the Secretary shall, subject to paragraph (2), by regulation classify such device.
(2)(A) A regulation under paragraph (1) classifying a device in class I shall prescribe which, if
any, of the requirements of section 510, 519 or 520(f) shall not apply to the device. A
regulation which makes a requirement of section 510, 519, or 520(f) inapplicable to a device
shall be accompanied by a statement of the reasons of the Secretary for making such
requirement inapplicable.
(B) A device described in subsection (c)(2)(C) shall be classified in class III unless the
Secretary determines that classification of the device in such class is not necessary to provide
reasonable assurance of its safety and effectiveness. A proposed regulation under paragraph
(1) classifying such a device in a class other than class III shall be accompanied by a full
statement of the reasons of the Secretary (and supporting documentation and data) for not
classifying such device in such class and an identification of the risks to health (if any)
presented by such device.
(3) In the case of devices classified in class II and devices classified under this subsection in
class III and described in section 515(b)(1) the Secretary may establish priorities which, in his
discretion, shall be used in applying sections 514 and 515, as appropriate, to such devices.
(e) Classification Changes
(1) Based on new information respecting a device, the Secretary may, upon his own initiative
or upon petition of an interested person, by regulation (A) change such device’s classification,
and (B) revoke, because of the change in classification, any regulation or requirement in effect
under section 514 or 515 with respect to such device. In the promulgation of such a regulation
respecting a device’s classification, the Secretary may secure from the panel to which the
device was last referred pursuant to subsection (c) a recommendation respecting the
proposed change in the device’s classification and shall publish in the Federal Register any
recommendation submitted to the Secretary by the panel respecting such change. A regulation
under this subsection changing the classification of a device from class III to class II may
provide that such classification shall not take effect until the effective date of a performance
standard established under section 514 for such device.
(2) By regulation promulgated under paragraph (1), the Secretary may change the
classification of a device from class III—
(A) to class II if the Secretary determines that special controls would provide reasonable
assurance of the safety and effectiveness of the device and that general controls would not
provide reasonable assurance of the safety and effectiveness of the device, or
(B) to class I if the Secretary determines that general controls would provide reasonable
assurance of the safety and effectiveness of the device.
(f) Initial Classification and Reclassification of Certain Devices
(1) Any device intended for human use which was not introduced or delivered for introduction
into interstate commerce for commercial distribution before the date of the enactment of this
section is classified in class III unless—
(A) the device—
(i) is within a type of device (I) which was introduced or delivered for introduction into interstate
commerce for commercial distribution before such date and which is to be classified pursuant
to subsection (b), or (II) which was not so introduced or delivered before such date and has
been classified in class I or II, and
(ii) is substantially equivalent to another device within such type, or
(B) the Secretary in response to a petition submitted under paragraph (3) has classified such
device in class I or II.
A device classified in class III under this paragraph shall be classified in that class until the
effective date of an order of the Secretary under paragraph (2) or (3) classifying the device in
class I or II.
(2)(A) Any person who submits a report under section 510(k) for a type of device that has not
been previously classified under this Act, and that is classified into class III under paragraph
(1), may request, within 30 days after receiving written notice of such a classification, the
Secretary to classify the device under the criteria set forth in subparagraphs (A) through (C) of
subsection (a)(1). The person may, in the request, recommend to the Secretary a classification
for the device. Any such request shall describe the device and provide detailed information
and reasons for the recommended classification.
(B)(i) Not later than 60 days after the date of the submission of the request under
subparagraph (A), the Secretary shall by written order classify the device involved. Such
classification shall be the initial classification of the device for purposes of paragraph (1) and
any device classified under this paragraph shall be a predicate device for determining
substantial equivalence under paragraph (1).
(ii) A device that remains in class III under this subparagraph shall be deemed to be
adulterated within the meaning of section 501(f)(1)(B) until approved under section 515 or
exempted from such approval under section 520(g).
(C) Within 30 days after the issuance of an order classifying a device under this paragraph, the
Secretary shall publish a notice in the Federal Register announcing such classification.
(3)(A) The Secretary may initiate the reclassification of a device classified into class III under
paragraph (1) of this subsection or the manufacturer or importer of a device classified under
paragraph (1) may petition the Secretary (in such form and manner as he shall prescribe) for
the issuance of an order classifying the device in class I or class II. Within thirty days of the
filing of such a petition, the Secretary shall notify the petitioner of any deficiencies in the
petition which prevent the Secretary from making a decision on the petition.
(B)(i) Upon determining that a petition does not contain any deficiency which prevents the
Secretary from making a decision on the petition, the Secretary may for good cause shown
refer the petition to an appropriate panel established or authorized to be used under
subsection (b). A panel to which such a petition has been referred shall not later than ninety
days after the referral of the petition make a recommendation to the Secretary respecting
approval or denial of the petition. Any such recommendation shall contain (I) a summary of the
reasons for the recommendation, (II) a summary of the data upon which the recommendation
is based, and (III) an identification of the risks to health (if any) presented by the device with
respect to which the petition was filed. In the case of a petition for a device which is intended to
be implanted in the human body or which is purported or represented to be for a use in
supporting or sustaining human life, the panel shall recommend that the petition be denied
unless the panel determines that the classification in class III of the device is not necessary to
provide reasonable assurance of its safety and effectiveness. If the panel recommends that
such petition be approved, it shall in its recommendation to the Secretary set forth its reasons
for such recommendation.
(ii) The requirements of paragraphs (1) and (2) of subsection (c) (relating to opportunities for
submission of data and views and recommendations respecting priorities and exemptions from
sections 510, 519, and 520(f)) shall apply with respect to consideration by panels of petitions
submitted under subparagraph (A).
(C)(i) Within ninety days from the date the Secretary receives the recommendation of a panel
respecting a petition (but not later than 210 days after the filing of such petition) the Secretary
shall by order deny or approve the petition. If the Secretary approves the petition, the
Secretary shall order the classification of the device into class I or class II in accordance with
the criteria prescribed by subsection (a)(1)(A) or (a)(1)(B). In the case of a petition for a device
which is intended to be implanted in the human body or which is purported or represented to
be for a use in supporting or sustaining human life, the Secretary shall deny the petition unless
the Secretary determines that the classification in class III of the device is not necessary to
provide reasonable assurance of its safety and effectiveness. An order approving such petition
shall be accompanied by a full statement of the reasons of the Secretary (and supporting
documentation and data) for approving the petition and an identification of the risks to health (if
any) presented by the device to which such order applies.
(ii) The requirements of paragraphs (1) and (2)(A) of subsection (d) (relating to publication of
recommendations, opportunity for submission of comments, and exemption from sections 510,
519, and 520(f)) shall apply with respect to action by the Secretary on petitions submitted
under subparagraph (A).
(4) If a manufacturer reports to the Secretary under section 510(k) that a device is substantially
equivalent to another device—
(A) which the Secretary has classified as a class III device under subsection (b),
(B) which was introduced or delivered for introduction into interstate commerce for commercial
distribution before December 1, 1990, and
(C) for which no final regulation requiring premarket approval has been promulgated under
section 515(b),
the manufacturer shall certify to the Secretary that the manufacturer has conducted a
reasonable search of all information known or otherwise available to the manufacturer
respecting such other device and has included in the report under section 510(k) a summary of
and a citation to all adverse safety and effectiveness data respecting such other device and
respecting the device for which the section 510(k) report is being made and which has not
been submitted to the Secretary under section 519. The Secretary may require the
manufacturer to submit the adverse safety and effectiveness data described in the report.
(5) The Secretary may not withhold a determination of the initial classification of a device
under paragraph (1) because of a failure to comply with any provision of this Act unrelated to a
substantial equivalence decision, including a finding that the facility in which the device is
manufactured is not in compliance with good manufacturing requirements as set forth in
regulations of the Secretary under section 520(f) (other than a finding that there is a
substantial likelihood that the failure to comply with such regulations will potentially present a
serious risk to human health).
(g) Information. Within sixty days of the receipt of a written request of any person for
information respecting the class in which a device has been classified or the requirements
applicable to a device under this Act, the Secretary shall provide such person a written
statement of the classification (if any) of such device and the requirements of this Act
applicable to the device.
(h) Definitions. For purposes of this section and sections 501, 510, 514, 515, 516, 519, and
520—
(1) a reference to "general controls" is a reference to the controls authorized by or under
sections 501, 502, 510, 516, 518, 519, and 520,
(2) a reference to "class I," "class II," or "class III" is a reference to a class of medical devices
described in subparagraph (A), (B), or (C) of subsection (a)(1), and
(3) a reference to a "panel under section 513" is a reference to a panel established or
authorized to be used under this section.
(i) Substantial Equivalence
(1)(A) For purposes of determinations of substantial equivalence under subsection (f) and
section 520(l), the term "substantially equivalent" or "substantial equivalence" means, with
respect to a device being compared to a predicate device, that the device has the same
intended use as the predicate device and that the Secretary by order has found that the
device—
(i) has the same technological characteristics as the predicate device, or
(ii)(I) has different technological characteristics and the information submitted that the device is
substantially equivalent to the predicate device contains information, including appropriate
clinical or scientific data if deemed necessary by the Secretary or a person accredited under
section 523, that demonstrates that the device is as safe and effective as a legally marketed
device, and (II) does not raise different questions of safety and effectiveness than the
predicate device.
(B) For purposes of subparagraph (A), the term "different technological characteristics" means,
with respect to a device being compared to a predicate device, that there is a significant
change in the materials, design, energy source, or other features of the device from those of
the predicate device.
(C) To facilitate reviews of reports submitted to the Secretary under section 510(k), the
Secretary shall consider the extent to which reliance on postmarket controls may expedite the
classification of devices under subsection (f)(1) of this section.
(D) Whenever the Secretary requests information to demonstrate that devices with differing
technological characteristics are substantially equivalent, the Secretary shall only request
information that is necessary to making substantial equivalence determinations. In making
such request, the Secretary shall consider the least burdensome means of demonstrating
substantial equivalence and request information accordingly.
(E)(i) Any determination by the Secretary of the intended use of a device shall be based upon
the proposed labeling submitted in a report for the device under section 510(k). However,
when determining that a device can be found substantially equivalent to a legally marketed
device, the director of the organizational unit responsible for regulating devices (in this
subparagraph referred to as the "Director") may require a statement in labeling that provides
appropriate information regarding a use of the device not identified in the proposed labeling if,
after providing an opportunity for consultation with the person who submitted such report, the
Director determines and states in writing—
(I) that there is a reasonable likelihood that the device will be used for an intended use not
identified in the proposed labeling for the device; and
(II) that such use could cause harm.
(ii) Such determination shall—
(I) be provided to the person who submitted the report within 10 days from the date of the
notification of the Director’s concerns regarding the proposed labeling;
(II) specify the limitations on the use of the device not included in the proposed labeling; and
(III) find the device substantially equivalent if the requirements of subparagraph (A) are met
and if the labeling for such device conforms to the limitations specified in subclause (II).
(iii) The responsibilities of the Director under this subparagraph may not be delegated.
(iv) This subparagraph has no legal effect after the expiration of the five-year period beginning
on the date of the enactment of the Food and Drug Administration Modernization Act of 1997.
(F) Not later than 270 days after the date of the enactment of the Food and Drug
Administration Modernization Act of 1997, the Secretary shall issue guidance specifying the
general principles that the Secretary will consider in determining when a specific intended use
of a device is not reasonably included within a general use of such device for purposes of a
determination of substantial equivalence under subsection (f) or section 520(l).
(2) A device may not be found to be substantially equivalent to a predicate device that has
been removed from the market at the initiative of the Secretary or that has been determined to
be misbranded or adulterated by a judicial order.
(3)(A) As part of a submission under section 510(k) respecting a device, the person required to
file a premarket notification under such section shall provide an adequate summary of any
information respecting safety and effectiveness or state that such information will be made
available upon request by any person.
(B) Any summary under subparagraph (A) respecting a device shall contain detailed
information regarding data concerning adverse health effects and shall be made available to
the public by the Secretary within 30 days of the issuance of a determination that such device
is substantially equivalent to another device.
PERFORMANCE STANDARDS
SEC. 514. [21 U.S.C. 360d ] (a) Provisions of Standards
(1) The special controls required by section 513(a)(1)(B) shall include performance standards
for a class II device if the Secretary determines that a performance standard is necessary to
provide reasonable assurance of the safety and effectiveness of the device. A class III device
may also be considered a class II device for purposes of establishing a standard for the device
under subsection (b) if the device has been reclassified as a class II device under a regulation
under section 513(e) but such regulation provides that the reclassification is not to take effect
until the effective date of such a standard for the device.
(2) A performance standard established under subsection (b) for a device—
(A) shall include provisions to provide reasonable assurance of its safe and effective
performance;
(B) shall, where necessary to provide reasonable assurance of its safe and effective
performance, include—
(i) provisions respecting the construction, components, ingredients, and properties of the
device and its compatibility with power systems and connections to such systems,
(ii) provisions for the testing (on a sample basis or, if necessary, on an individual basis) of the
device or, if it is determined that no other more practicable means are available to the
Secretary to assure the conformity of the device to the standard, provisions for the testing (on
a sample basis or, if necessary, on an individual basis) by the Secretary or by another person
at the direction of the Secretary,
(iii) provisions for the measurement of the performance characteristics of the device,
(iv) provisions requiring that the results of each or of certain of the tests of the device required
to be made under clause (ii) show that the device is in conformity with the portions of the
standard for which the test or tests were required, and
(v) a provision requiring that the sale and distribution of the device be restricted but only to the
extent that the sale and distribution of a device may be restricted under a regulation under
section 520(e); and
(C) shall, where appropriate, require the use and prescribe the form and content of labeling for
the proper installation, maintenance, operation, and use of the device.
(3) The Secretary shall provide for periodic evaluation of performance standards established
under subsection (b) to determine if such standards should be changed to reflect new medical,
scientific, or other technological data.
(4) In carrying out his duties under this subsection and subsection (b), the Secretary shall, to
the maximum extent practicable—
(A) use personnel, facilities, and other technical support available in other Federal agencies,
(B) consult with other Federal agencies concerned with standard-setting and other nationally
or internationally recognized standard-setting entities, and
(C) invite appropriate participation, through joint or other conferences, workshops, or other
means, by informed persons representative of scientific, professional, industry, or consumer
organizations who in his judgment can make a significant contribution.
(b) Establishment of a Standard
(1)(A) The Secretary shall publish in the Federal Register a notice of proposed rulemaking for
the establishment, amendment, or revocation of any performance standard for a device.
(B) A notice of proposed rulemaking for the establishment or amendment of a performance
standard for a device shall—
(i) set forth a finding with supporting justification that the performance standard is appropriate
and necessary to provide reasonable assurance of the safety and effectiveness of the device,
(ii) set forth proposed findings with respect to the risk of illness or injury that the performance
standard is intended to reduce or eliminate,
(iii) invite interested persons to submit to the Secretary, within 30 days of the publication of the
notice, requests for changes in the classification of the device pursuant to section 513(e)
based on new information relevant to the classification, and
(iv) invite interested persons to submit an existing performance standard for the device,
including a draft or proposed performance standard, for consideration by the Secretary.
(C) A notice of proposed rulemaking for the revocation of a performance standard shall set
forth a finding with supporting justification that the performance standard is no longer
necessary to provide reasonable assurance of the safety and effectiveness of a device.
(D) The Secretary shall provide for a comment period of not less than 60 days.
(2) If, after publication of a notice in accordance with paragraph (1), the Secretary receives a
request for a change in the classification of the device, the Secretary shall, within 60 days of
the publication of the notice, after consultation with the appropriate panel under section 513,
either deny the request or give notice of an intent to initiate such change under section 513(e).
(3)(A) After the expiration of the period for comment on a notice of proposed rulemaking
published under paragraph (1) respecting a performance standard and after consideration of
such comments and any report from an advisory committee under paragraph (5), the
Secretary shall (i) promulgate a regulation establishing a performance standard and publish in
the Federal Register findings on the matters referred to in paragraph (1), or (ii) publish a notice
terminating the proceeding for the development of the standard together with the reasons for
such termination. If a notice of termination is published, the Secretary shall (unless such notice
is issued because the device is a banned device under section 516) initiate a proceeding
under section 513(e) to reclassify the device subject to the proceeding terminated by such
notice.
(B) A regulation establishing a performance standard shall set forth the date or dates upon
which the standard shall take effect, but no such regulation may take effect before one year
after the date of its publication unless (i) the Secretary determines that an earlier effective date
is necessary for the protection of the public health and safety, or (ii) such standard has been
established for a device which, effective upon the effective date of the standard, has been
reclassified from class III to class II. Such date or dates shall be established so as to minimize,
consistent with the public health and safety, economic loss to, and disruption or dislocation of,
domestic and international trade.
(4)(A) The Secretary, upon his own initiative or upon petition of an interested person may by
regulation, promulgated in accordance with the requirements of paragraphs (1), (2), and (3)(B)
of this subsection, amend or revoke a performance standard.
(B) The Secretary may declare a proposed amendment of a performance standard to be
effective on and after its publication in the Federal Register and until the effective date of any
final action taken on such amendment if he determines that making it so effective is in the
public interest. A proposed amendment of a performance standard made so effective under
the preceding sentence may not prohibit, during the period in which it is so effective, the
introduction or delivery for introduction into interstate commerce of a device which conforms to
such standard without the change or changes provided by such proposed amendment.
(5)(A) The Secretary—
(i) may on his own initiative refer a proposed regulation for the establishment, amendment, or
revocation of a performance standard, or
(ii) shall, upon the request of an interested person which demonstrates good cause for referral
and which is made before the expiration of the period for submission of comments on such
proposed regulation refer such proposed regulation, to an advisory committee of experts,
established pursuant to subparagraph (B) for a report and recommendation with respect to any
matter involved in the proposed regulation which requires the exercise of scientific judgment. If
a proposed regulation is referred under this subparagraph to an advisory committee, the
Secretary shall provide the advisory committee with the data and information on which such
proposed regulation is based. The advisory committee shall, within sixty days of the referral of
a proposed regulation and after independent study of the data and information furnished to it
by the Secretary and other data and information before it, submit to the Secretary a report and
recommendation respecting such regulation, together with all underlying data and information
and a statement of the reason or basis for the recommendation. A copy of such report and
recommendation shall be made public by the Secretary.
(B) The Secretary shall establish advisory committees (which may not be panels under section
513) to receive referrals under subparagraph (A). The Secretary shall appoint as members of
any such advisory committee persons qualified in the subject matter to be referred to the
committee and of appropriately diversified professional background, except that the Secretary
may not appoint to such a committee any individual who is in the regular full-time employ of the
United States and engaged in the administration of this Act. Each such committee shall include
as nonvoting members a representative of consumer interests and a representative of
interests of the device manufacturing industry. Members of an advisory committee who are not
officers or employees of the United States, while attending conferences or meetings of their
committee or otherwise serving at the request of the Secretary, shall be entitled to receive
compensation at rates to be fixed by the Secretary, which rates may not exceed the daily
equivalent of the rate in effect for grade GS–18 of the General Schedule 2 , for each day
(including travel time) they are so engaged; and while so serving away from their homes or
regular places of business each member may be allowed travel expenses, including per diem
in lieu of subsistence, as authorized by section 5703 of title 5 of the United States Code for
persons in the Government service employed intermittently. The Secretary shall designate one
of the members of each advisory committee to serve as chairman thereof. The Secretary shall
furnish each advisory committee with clerical and other assistance, and shall by regulation
prescribe the procedures to be followed by each such committee in acting on referrals made
under subparagraph (A).
(c) Recognition of a Standard
(1)(A) In addition to establishing a performance standard under this section, the Secretary
shall, by publication in the Federal Register, recognize all or part of an appropriate standard
established by a nationally or internationally recognized standard development organization
for which a person may submit a declaration of conformity in order to meet a premarket
submission requirement or other requirement under this Act to which such standard is
applicable.
(B) If a person elects to use a standard recognized by the Secretary under subparagraph (A) to
meet the requirements described in such subparagraph, the person shall provide a declaration
of conformity to the Secretary that certifies that the device is in conformity with such standard.
A person may elect to use data, or information, other than data required by a standard
recognized under subparagraph (A) to meet any requirement regarding devices under this Act.
(2) The Secretary may withdraw such recognition of a standard through publication of a notice
in the Federal Register if the Secretary determines that the standard is no longer appropriate
for meeting a requirement regarding devices under this Act.
(3)(A) Subject to subparagraph (B), the Secretary shall accept a declaration of conformity that
a device is in conformity with a standard recognized under paragraph (1) unless the Secretary
finds—
(i) that the data or information submitted to support such declaration does not demonstrate that
the device is in conformity with the standard identified in the declaration of conformity; or
(ii) that the standard identified in the declaration of conformity is not applicable to the particular
device under review.
(B) The Secretary may request, at any time, the data or information relied on by the person to
make a declaration of conformity with respect to a standard recognized under paragraph (1).
(C) A person making a declaration of conformity with respect to a standard recognized under
paragraph (1) shall maintain the data and information demonstrating conformity of the device
to the standard for a period of two years after the date of the classification or approval of the
device by the Secretary or a period equal to the expected design life of the device, whichever
is longer.
PREMARKET APPROVAL
SEC. 515. [21 U.S.C. 360e ] (a) General Requirement. A class III device—
(1) which is subject to a regulation promulgated under subsection (b); or
(2) which is a class III device because of section 513(f), is required to have, unless exempt
under section 520(g), an approval under this section of an application for premarket approval
or, as applicable, an approval under subsection (c)(2) of a report seeking premarket approval.
(b) Regulation To Require Premarket Approval
(1) In the case of a class III device which—
(A) was introduced or delivered for introduction into interstate commerce for commercial
distribution before the date of enactment of this section; or
(B) is (i) of a type so introduced or delivered, and (ii) is substantially equivalent to another
device within that type;
the Secretary shall by regulation, promulgated in accordance with this subsection, require that
such device have an approval under this section of an application for premarket approval.
(2)(A) A proceeding for the promulgation of a regulation under paragraph (1) respecting a
device shall be initiated by the publication in the Federal Register of a notice of proposed
rulemaking. Such notice shall contain—
(i) the proposed regulation;
(ii) proposed findings with respect to the degree of risk of illness or injury designed to be
eliminated or reduced by requiring the device to have an approved application for Premarket
approval and the benefit to the public from use of the device;
(iii) opportunity for the submission of comments on the proposed regulation and the proposed
findings; and
(iv) opportunity to request a change in the classification of the device based on new
information relevant to the classification of the device.
(B) If, within fifteen days after publication of a notice under subparagraph (A), the Secretary
receives a request for a change in the classification of a device, he shall, within sixty days of
the publication of such notice and after consultation with the appropriate panel under section
513, by order published in the Federal Register, either deny the request for change in
classification or give notice of his intent to initiate such a change under section 513(e).
(3) After the expiration of the period for comment on a proposed regulation and proposed
findings published under paragraph (2) and after consideration of comments submitted on
such proposed regulation and findings, the Secretary shall (A) promulgate such regulation and
publish in the Federal Register findings on the matters referred to in paragraph (2)(A)(ii), or (B)
publish a notice terminating the proceeding for the promulgation of the regulation together with
the reasons for such termination. If a notice of termination is published, the Secretary shall
(unless such notice is issued because the device is a banned device under section 516)
initiate a proceeding under section 513(e) to reclassify the device subject to the proceeding
terminated by such notice.
(4) The Secretary, upon his own initiative or upon petition of an interested person, may by
regulation amend or revoke any regulation promulgated under this subsection. A regulation to
amend or revoke a regulation under this subsection shall be promulgated in accordance with
the requirements prescribed by this subsection for the promulgation of the regulation to be
amended or revoked.
(c) Application for Premarket Approval
(1) Any person may file with the Secretary an application for premarket approval for a class III
device. Such an application for a device shall contain—
(A) full reports of all information, published or known to or which should reasonably be known
to the applicant, concerning investigations which have been made to show whether or not such
device is safe and effective;
(B) a full statement of the components, ingredients, and properties and of the principle or
principles of operation, of such device;
(C) a full description of the methods used in, and the facilities and controls used for, the
manufacture, processing, and, when relevant, packing and installation of, such device;
(D) an identifying reference to any performance standard under section 514 which would be
applicable to any aspect of such device if it were a class II device, and either adequate
information to show that such aspect of such device fully meets such performance standard or
adequate information to justify any deviation from such standard;
(E) such samples of such device and of components thereof as the Secretary may reasonably
require, except that where the submission of such samples is impracticable or unduly
burdensome, the requirement of this subparagraph may be met by the submission of complete
information concerning the location of one or more such devices readily available for
examination and testing;
(F) specimens of the labeling proposed to be used for such device; and
(G) such other information relevant to the subject matter of the application as the Secretary,
with the concurrence of the appropriate panel under section 513, may require.
(2)(A) Any person may file with the Secretary a report seeking premarket approval for a class
III device referred to in subsection (a) that is a reprocessed single-use device. Such a report
shall contain the following:
(i) The device name, including both the trade or proprietary name and the common or usual
name.
(ii) The establishment registration number of the owner or operator submitting the report.
(iii) Actions taken to comply with performance standards under section 514.
(iv) Proposed labels, labeling, and advertising sufficient to describe the device, its intended
use, and directions for use.
(v) Full reports of all information, published or known to or which should be reasonably known
to the applicant, concerning investigations which have been made to show whether or not the
device is safe or effective.
(vi) A description of the device's components, ingredients, and properties.
(vii) A full description of the methods used in, and the facilities and controls used for, the
reprocessing and packing of the device.
(viii) Such samples of the device that the Secretary may reasonably require.
(ix) A financial certification or disclosure statement or both, as required by part 54 of title 21,
Code of Federal Regulations.
(x) A statement that the applicant believes to the best of the applicant's knowledge that all data
and information submitted to the Secretary are truthful and accurate and that no material fact
has been omitted in the report.
(xi) Any additional data and information, including information of the type required in paragraph
(1) for an application under such paragraph, that the Secretary determines is necessary to
determine whether there is reasonable assurance of safety and effectiveness for the
reprocessed device.
(xii) Validation data described in section 510(o)(1)(A) that demonstrates that the reasonable
assurance of the safety or effectiveness of the device will remain after the maximum number of
times the device is reprocessed as intended by the person submitting such report.
(B) In the case of a class III device referred to in subsection (a) that is a reprocessed
single-use device:
(i) Subparagraph (A) of this paragraph applies in lieu of paragraph (1).
(ii) Subject to clause (i), the provisions of this section apply to a report under subparagraph (A)
to the same extent and in the same manner as such provisions apply to an application under
paragraph (1).
(iii) Each reference in other sections of this Act to an application under this section, other than
such a reference in section 737 or 738, shall be considered to be a reference to a report under
subparagraph (A).
(iv) Each reference in other sections of this Act to a device for which an application under this
section has been approved, or has been denied, suspended, or withdrawn, other than such a
reference in section 737 or 738, shall be considered to be a reference to a device for which a
report under subparagraph (A) has been approved, or has been denied, suspended, or
withdrawn, respectively.
(3) Upon receipt of an application meeting the requirements set forth in paragraph (1), the
Secretary—
(A) may on the Secretary’s own initiative, or
(B) shall, upon the request of an applicant unless the Secretary finds that the information in the
application which would be reviewed by a panel substantially duplicates information which has
previously been reviewed by a panel appointed under section 513, refer such application to the
appropriate panel under section 513 for study and for submission (within such period as he
may establish) of a report and recommendation respecting approval of the application,
together with all underlying data and the reasons or basis for the recommendation.
(4)(A) Prior to the submission of an application under this subsection, the Secretary shall
accept and review any portion of the application that the applicant and the Secretary agree is
complete, ready, and appropriate for review, except that such requirement does not apply, and
the Secretary has discretion whether to accept and review such portion, during any period in
which, under section 738(g), the Secretary does not have the authority to collect fees under
section 738(a).
(B) Each portion of a submission reviewed under subparagraph (A) and found acceptable by
the Secretary shall not be further reviewed after receipt of an application that satisfies the
requirements of paragraph (1), unless an issue of safety unless an issue of a significant safety
or effectiveness provides the Secretary reason to review such accepted portion.
(C) Whenever the Secretary determines that a portion of a submission under subparagraph (A)
is unacceptable, the Secretary shall, in writing, provide to the applicant a description of any
deficiencies in such portion and identify the information that is required to correct these
deficiencies, unless the applicant is no longer pursuing the application. Where appropriate, the
Secretary shall ensure that such panel includes, or consults with, one or more pediatric
experts.
(d) Action on an Application for Premarket Approval
(1)(A) As promptly as possible, but in no event later than one hundred and eighty days after
the receipt of an application under subsection (c) (except as provided in section 520(l)(3)(D)(ii)
or unless, in accordance with subparagraph (B)(i), an additional period as agreed upon by the
Secretary and the applicant), the Secretary, after considering the report and recommendation
submitted under paragraph (2) of such subsection, shall—
(i) issue an order approving the application if he finds that none of the grounds for denying
approval specified in paragraph (2) of this subsection applies; or
(ii) deny approval of the application if he finds (and sets forth the basis for such finding as part
of or accompanying such denial) that one or more grounds for denial specified in paragraph (2)
of this subsection apply.
In making the determination whether to approve or deny the application, the Secretary shall
rely on the conditions of use included in the proposed labeling as the basis for determining
whether or not there is a reasonable assurance of safety and effectiveness, if the proposed
labeling is neither false nor misleading. In determining whether or not such labeling is false or
misleading, the Secretary shall fairly evaluate all material facts pertinent to the proposed
labeling.
(B)(i) The Secretary may not enter into an agreement to extend the period in which to take
action with respect to an application submitted for a device subject to a regulation promulgated
under subsection (b) unless he finds that the continued availability of the device is necessary
for the public health.
(ii) An order approving an application for a device may require as a condition to such approval
that the sale and distribution of the device be restricted but only to the extent that the sale and
distribution of a device may be restricted under a regulation under section 520(e).
(iii) The Secretary shall accept and review statistically valid and reliable data and any other
information from investigations conducted under the authority of regulations required by
section 520(g) to make a determination of whether there is a reasonable assurance of safety
and effectiveness of a device subject to a pending application under this section if—
(I) the data or information is derived from investigations of an earlier version of the device, the
device has been modified during or after the investigations (but prior to submission of an
application under subsection (c)) and such a modification of the device does not constitute a
significant change in the design or in the basic principles of operation of the device that would
invalidate the data or information; or
(II) the data or information relates to a device approved under this section, is available for use
under this Act, and is relevant to the design and intended use of the device for which the
application is pending.
(2) The Secretary shall deny approval of an application for a device if, upon the basis of the
information submitted to the Secretary as part of the application and any other information
before him with respect to such device, the Secretary finds that—
(A) there is a lack of a showing of reasonable assurance that such device is safe under the
conditions of use prescribed, recommended, or suggested in the proposed labeling thereof;
(B) there is a lack of a showing of reasonable assurance that the device is effective under the
conditions of use prescribed, recommended, or suggested in the proposed labeling thereof;
(C) the methods used in, or the facilities or controls used for, the manufacture, processing,
packing, or installation of such device do not conform to the requirements of section 520(f);
(D) based on a fair evaluation of all material facts, the proposed labeling is false or misleading
in any particular; or
(E) such device is not shown to conform in all respects to a performance standard in effect
under section 514 compliance with which is a condition to approval of the application and there
is a lack of adequate information to justify the deviation from such standard.
Any denial of an application shall, insofar as the Secretary determines to be practicable, be
accompanied by a statement informing the applicant of the measures required to place such
application in approvable form (which measures may include further research by the applicant
in accordance with one or more protocols prescribed by the Secretary).
(3)(A)(i) The Secretary shall, upon the written request of an applicant, meet with the applicant,
not later than 100 days after the receipt of an application that has been filed as complete under
subsection (c), to discuss the review status of the application.
(ii) The Secretary shall, in writing and prior to the meeting, provide to the applicant a
description of any deficiencies in the application that, at that point, have been identified by the
Secretary based on an interim review of the entire application and identify the information that
is required to correct those deficiencies.
(iii) The Secretary shall notify the applicant promptly of—
(I) any additional deficiency identified in the application, or
(II) any additional information required to achieve completion of the review and final action on
the application,
that was not described as a deficiency in the written description provided by the Secretary
under clause (ii).
(B) The Secretary and the applicant may, by mutual consent, establish a different schedule for
a meeting required under this paragraph.
(4) An applicant whose application has been denied approval may, by petition filed on or
before the thirtieth day after the date upon which he receives notice of such denial, obtain
review thereof in accordance with either paragraph (1) or (2) of subsection (g), and any
interested person may obtain review, in accordance with paragraph (1) or (2) of subsection (g),
of an order of the Secretary approving an application.
(5) In order to provide for more effective treatment or diagnosis of life-threatening or
irreversibly debilitating human diseases or conditions, the Secretary shall provide review
priority for devices—
(A) representing breakthrough technologies,
(B) for which no approved alternatives exist,
(C) which offer significant advantages over existing approved alternatives, or
(D) the availability of which is in the best interest of the patients.
(6)(A)(i) A supplemental application shall be required for any change to a device subject to an
approved application under this subsection that affects safety or effectiveness, unless such
change is a modification in a manufacturing procedure or method of manufacturing and the
holder of the approved application submits a written notice to the Secretary that describes in
detail the change, summarizes the data or information supporting the change, and informs the
Secretary that the change has been made under the requirements of section 520(f).
(ii) The holder of an approved application who submits a notice under clause (i) with respect to
a manufacturing change of a device may distribute the device 30 days after the date on which
the Secretary receives the notice, unless the Secretary within such 30-day period notifies the
holder that the notice is not adequate and describes such further information or action that is
required for acceptance of such change. If the Secretary notifies the holder that a
supplemental application is required, the Secretary shall review the supplement within 135
days after the receipt of the supplement. The time used by the Secretary to review the notice
of the manufacturing change shall be deducted from the 135-day review period if the notice
meets appropriate content requirements for Premarket approval supplements.
(B)(i) Subject to clause (ii), in reviewing a supplement to an approved application, for an
incremental change to the design of a device that affects safety or effectiveness, the Secretary
shall approve such supplement if—
(I) nonclinical data demonstrate that the design modification creates the intended additional
capacity, function, or performance of the device; and
(II) clinical data from the approved application and any supplement to the approved application
provide a reasonable assurance of safety and effectiveness for the changed device.
(ii) The Secretary may require, when necessary, additional clinical data to evaluate the design
modification of the device to provide a reasonable assurance of safety and effectiveness.
(e) Withdrawal and Temporary Suspension of Approval of Application
(1) The Secretary shall, upon obtaining, where appropriate, advice on scientific matters from a
panel or panels under section 513, and after due notice and opportunity for informal hearing to
the holder of an approved application for a device, issue an order withdrawing approval of the
application if the Secretary finds—
(A) that such device is unsafe or ineffective under the conditions of use prescribed,
recommended, or suggested in the labeling thereof;
(B) on the basis of new information before him with respect to such device, evaluated together
with the evidence available to him when the application was approved, that there is a lack of a
showing of reasonable assurance that the device is safe or effective under the conditions of
use prescribed, recommended, or suggested in the labeling thereof;
(C) that the application contained or was accompanied by an untrue statement of a material
fact;
(D) that the applicant (i) has failed to establish a system for maintaining records, or has
repeatedly or deliberately failed to maintain records or to make reports, required by an
applicable regulation under section 519(a), (ii) has refused to permit access to, or copying or
verification of, such records as required by section 704, or (iii) has not complied with the
requirements of section 510;
(E) on the basis of new information before him with respect to such device, evaluated together
with the evidence before him when the application was approved, that the methods used in, or
the facilities and controls used for, the manufacture, processing, packing, or installation of
such device do not conform with the requirements of section 520(f) and were not brought into
conformity with such requirements within a reasonable time after receipt of written notice from
the Secretary of nonconformity;
(F) on the basis of new information before him, evaluated together with the evidence before
him when the application was approved, that the labeling of such device, based on a fair
evaluation of all material facts, is false or misleading in any particular and was not corrected
within a reasonable time after receipt of written notice from the Secretary of such fact; or
(G) on the basis of new information before him, evaluated together with the evidence before
him when the application was approved, that such device is not shown to conform in all
respects to a performance standard which is in effect under section 514 compliance with which
was a condition to approval of the application and that there is a lack of adequate information
to justify the deviation from such standard.
(2) The holder of an application subject to an order issued under paragraph (1) withdrawing
approval of the application may, by petition filed on or before the thirtieth day after the date
upon which he receives notice of such withdrawal, obtain review thereof in accordance with
either paragraph (1) or (2) of subsection (g).
(3) If, after providing an opportunity for an informal hearing, the Secretary determines there is
reasonable probability that the continuation of distribution of a device under an approved
application would cause serious, adverse health consequences or death, the Secretary shall
by order temporarily suspend the approval of the application approved under this section. If the
Secretary issues such an order, the Secretary shall proceed expeditiously under paragraph (1)
to withdraw such application.
(f) Product Development Protocol
(1) In the case of a class III device which is required to have an approval of an application
submitted under subsection (c), such device shall be considered as having such an approval if
a notice of completion of testing conducted in accordance with a product development protocol
approved under paragraph (4) has been declared completed under paragraph (6).
(2) Any person may submit to the Secretary a proposed product development protocol with
respect to a device. Such a protocol shall be accompanied by data supporting it. If, within thirty
days of the receipt of such a protocol, the Secretary determines that it appears to be
appropriate to apply the requirements of this subsection to the device with respect to which the
protocol is submitted, the Secretary—
(A) may, at the initiative of the Secretary, refer the proposed protocol to the appropriate panel
under section 513 for its recommendation respecting approval of the protocol; or
(B) shall so refer such protocol upon the request of the submitter, unless the Secretary finds
that the proposed protocol and accompanying data which would be reviewed by such panel
substantially duplicate a product development protocol and accompanying data which have
previously been reviewed by such a panel.
(3) A proposed product development protocol for a device may be approved only if—
(A) the Secretary determines that it is appropriate to apply the requirements of this subsection
to the device in lieu of the requirement of approval of an application submitted under
subsection (c); and
(B) the Secretary determines that the proposed protocol provides—
(i) a description of the device and the changes which may be made in the device,
(ii) a description of the preclinical trials (if any) of the device and a specification of (I) the results
from such trials to be required before the commencement of clinical trials of the device, and (II)
any permissible variations in preclinical trials and the results therefrom,
(iii) a description of the clinical trials (if any) of the device and a specification of (I) the results
from such trials to be required before the filing of a notice of completion of the requirements of
the protocol, and (II) any permissible variations in such trials and the results therefrom,
(iv) a description of the methods to be used in, and the facilities and controls to be used for, the
manufacture, processing, and when relevant, packing and installation of the device,
(v) an identifying reference to any performance standard under section 514 to be applicable to
any aspect of such device,
(vi) if appropriate, specimens of the labeling proposed to be used for such device,
(vii) such other information relevant to the subject matter of the protocol as the Secretary, with
the concurrence of the appropriate panel or panels under section 513, may require, and
(viii) a requirement for submission of progress reports and, when completed, records of the
trials conducted under the protocol which records are adequate to show compliance with the
protocol.
(4) The Secretary shall approve or disapprove a proposed product development protocol
submitted under paragraph (2) within one hundred and twenty days of its receipt unless an
additional period is agreed upon by the Secretary and the person who submitted the protocol.
Approval of a protocol or denial of approval of a protocol is final agency action subject to
judicial review under chapter 7 of title 5, United States Code.
(5) At any time after a product development protocol for a device has been approved pursuant
to paragraph (4), the person for whom the protocol was approved may submit a notice of
completion—
(A) stating
(i) his determination that the requirements of the protocol have been fulfilled and that, to the
best of his knowledge, there is no reason bearing on safety or effectiveness why the notice of
completion should not become effective, and
(ii) the data and other information upon which such determination was made, and
(B) setting forth the results of the trials required by the protocol and all the information required
by subsection (c)(1).
(6)(A) The Secretary may, after providing the person who has an approved protocol an
opportunity for an informal hearing and at any time prior to receipt of notice of completion of
such protocol, issue a final order to revoke such protocol if he finds that—
(i) such person has failed substantially to comply with the requirements of the protocol,
(ii) the results of the trials obtained under the protocol differ so substantially from the results
required by the protocol that further trials cannot be justified, or
(iii) the results of the trials conducted under the protocol or available new information do not
demonstrate that the device tested under the protocol does not present an unreasonable risk
to health and safety.
(B) After the receipt of a notice of completion of an approved protocol the Secretary shall,
within the ninety-day period beginning on the date such notice is received, by order either
declare the protocol completed or declare it not completed. An order declaring a protocol not
completed may take effect only after the Secretary has provided the person who has the
protocol opportunity for an informal hearing on the order. Such an order may be issued only if
the Secretary finds—
(i) such person has failed substantially to comply with the requirements of the protocol,
(ii) the results of the trials obtained under the protocol differ substantially from the results
required by the protocol, or
(iii) there is a lack of a showing of reasonable assurance of the safety and effectiveness of the
device under the conditions of use prescribed, recommended, or suggested in the proposed
labeling thereof.
(C) A final order issued under subparagraph (A) or (B) shall be in writing and shall contain the
reasons to support the conclusions thereof.
(7) At any time after a notice of completion has become effective, the Secretary may issue an
order (after due notice and opportunity for an informal hearing to the person for whom the
notice is effective) revoking the approval of a device provided by a notice of completion which
has become effective as provided in subparagraph (B) if he finds that any of the grounds listed
in subparagraphs (A) through (G) of subsection (e)(1) of this section apply. Each reference in
such subparagraphs to an application shall be considered for purposes of this paragraph as a
reference to a protocol and the notice of completion of such protocol, and each reference to
the time when an application was approved shall be considered for purposes of this paragraph
as a reference to the time when a notice of completion took effect.
(8) A person who has an approved protocol subject to an order issued under paragraph (6)(A)
revoking such protocol, a person who has an approved protocol with respect to which an order
under paragraph (6)(B) was issued declaring that the protocol had not been completed, or a
person subject to an order issued under paragraph
(7) revoking the approval of a device may, by petition filed on or before the thirtieth day after
the date upon which he receives notice of such order, obtain review thereof in accordance with
either paragraph (1) or (2) of subsection (g).
(g) Review
(1) Upon petition for review of—
(A) an order under subsection (d) approving or denying approval of an application or an order
under subsection (e) withdrawing approval of an application, or
(B) an order under subsection (f)(6)(A) revoking an approved protocol, under subsection
(f)(6)(B) declaring that an approved protocol has not been completed, or under subsection (f)(7)
revoking the approval of a device,
the Secretary shall, unless he finds the petition to be without good cause or unless a petition
for review of such order has been submitted under paragraph (2), hold a hearing, in
accordance with section 554 of title 5 of the United States Code, on the order. The panel or
panels which considered the application, protocol, or device subject to such order shall
designate a member to appear and testify at any such hearing upon request of the Secretary,
the petitioner, or the officer conducting the hearing, but this requirement does not preclude any
other member of the panel or panels from appearing and testifying at any such hearing. Upon
completion of such hearing and after considering the record established in such hearing, the
Secretary shall issue an order either affirming the order subject to the hearing or reversing
such order and, as appropriate, approving or denying approval of the application, reinstating
the application’s approval, approving the protocol, or placing in effect a notice of completion.
(2)(A) Upon petition for review of—
(i) an order under subsection (d) approving or denying approval of an application or an order
under subsection (e) withdrawing approval of an application, or
(ii) an order under subsection (f)(6)(A) revoking an approved protocol, under subsection
(f)(6)(B) declaring that an approved protocol has not been completed, or under subsection (f)(7)
revoking the approval of a device,
the Secretary shall refer the application or protocol subject to the order and the basis for the
order to an advisory committee of experts established pursuant to subparagraph (B) for a
report and recommendation with respect to the order. The advisory committee shall, after
independent study of the data and information furnished to it by the Secretary and other data
and information before it, submit to the Secretary a report and recommendation, together with
all underlying data and information and a statement of the reasons or basis for the
recommendation. A copy of such report shall be promptly supplied by the Secretary to any
person who petitioned for such referral to the advisory committee.
(B) The Secretary shall establish advisory committees (which may not be panels under section
513) to receive referrals under subparagraph (A). The Secretary shall appoint as members of
any such advisory committee persons qualified in the subject matter to be referred to the
committee and of appropriately diversified professional backgrounds, except that the
Secretary may not appoint to such a committee any individual who is in the regular full-time
employ of the United States and engaged in the administration of this Act. Members of an
advisory committee (other than officers or employees of the United States), while attending
conferences or meetings of their committee or otherwise serving at the request of the
Secretary, shall be entitled to receive compensation at rates to be fixed by the Secretary which
rates may not exceed the daily equivalent for grade GS–18 of the General Schedule for each
day (including travel time) they are so engaged; and while so serving away from their homes or
regular places of business each member may be allowed travel expenses, including per diem
in lieu of subsistence, as authorized by section 5703 of title 5 of the United States Code for
persons in the Government service employed intermittently. The Secretary shall designate the
chairman of an advisory committee from its members. The Secretary shall furnish each
advisory committee with clerical and other assistance, and shall by regulation prescribe the
procedures to be followed by each such committee in acting on referrals made under
subparagraph (A).
(C) The Secretary shall make public the report and recommendation made by an advisory
committee with respect to an application and shall by order, stating the reasons therefor, either
affirm the order referred to the advisory committee or reverse such order and, if appropriate,
approve or deny approval of the application, reinstate the application’s approval, approve the
protocol, or place in effect a notice of completion.
(h) Service of Orders. Orders of the Secretary under this section shall be served (1) in person
by any officer or employee of the department designated by the Secretary, or (2) by mailing the
order by registered mail or certified mail addressed to the applicant at his last known address
in the records of the Secretary.
(i) Revision
(1) Before December 1, 1995, the Secretary shall by order require manufacturers of devices,
which were introduced or delivered for introduction into interstate commerce for commercial
distribution before May 28, 1976, and which are subject to revision of classification under
paragraph (2), to submit to the Secretary a summary of and citation to any information known
or otherwise available to the manufacturer respecting such devices, including adverse safety
or effectiveness information which has not been submitted under section 519. The Secretary
may require the manufacturer to submit the adverse safety or effectiveness data for which a
summary and citation were submitted, if such data are available to the manufacturer.
(2) After the issuance of an order under paragraph (1) but before December 1, 1995, the
Secretary shall publish a regulation in the Federal Register for each device—
(A) which the Secretary has classified as a class III device, and
(B) for which no final regulation has been promulgated under section 515(b),
revising the classification of the device so that the device is classified into class I or class II,
unless the regulation requires the device to remain in class III. In determining whether to revise
the classification of a device or to require a device to remain in class III, the Secretary shall
apply the criteria set forth in section 513(a). Before the publication of a regulation requiring a
device to remain in class III or revising its classification, the Secretary shall publish a proposed
regulation respecting the classification of a device under this paragraph and provide
reasonable opportunity for the submission of comments on any such regulation. No regulation
requiring a device to remain in class III or revising its classification may take effect before the
expiration of 90 days from the date of its publication in the Federal Register as a proposed
regulation.
(3) The Secretary shall, as promptly as is reasonably achievable, but not later than 12 months
after the effective date of the regulation requiring a device to remain in class III, establish a
schedule for the promulgation of a section 515(b) regulation for each device which is subject to
the regulation requiring the device to remain in class III.
BANNED DEVICES
SEC. 516. [21 U.S.C. 360f ] (a) General Rule. Whenever the Secretary finds, on the basis of all
available data and information, that—
(1) a device intended for human use presents substantial deception or an unreasonable and
substantial risk of illness or injury; and
(2) in the case of substantial deception or an unreasonable and substantial risk of illness or
injury which the Secretary determined could be corrected or eliminated by labeling or change
in labeling and with respect to which the Secretary provided written notice to the manufacturer
specifying the deception or risk of illness or injury, the labeling or change in labeling to correct
the deception or eliminate or reduce such risk, and the period within which such labeling or
change in labeling was to be done, such labeling or change in labeling was not done within
such period;
he may initiate a proceeding to promulgate a regulation to make such device a banned device.
(b) Special Effective Date. The Secretary may declare a proposed regulation under subsection
(a) to be effective upon its publication in the Federal Register and until the effective date of any
final action taken respecting such regulation if (1) he determines, on the basis of all available
data and information, that the deception or risk of illness or injury associated with the use of
the device which is subject to the regulation presents an unreasonable, direct, and substantial
danger to the health of individuals, and (2) before the date of the publication of such regulation,
the Secretary notifies the manufacturer of such device that such regulation is to be made so
effective. If the Secretary makes a proposed regulation so effective, he shall, as expeditiously
as possible, give interested persons prompt notice of his action under this subsection, provide
reasonable opportunity for an informal hearing on the proposed regulation, and either affirm,
modify, or revoke such proposed regulation.
JUDICIAL REVIEW
SEC. 517. [21 U.S.C. 360g ] (a) Application of Section. Not later than thirty days after—
(1) the promulgation of a regulation under section 513 classifying a device in class I or
changing the classification of a device to class I or an order under subsection (f)(2) of such
section reclassifying a device or denying a petition for reclassification of a device,
(2) the promulgation of a regulation under section 514 establishing, amending, or revoking a
performance standard for a device,
(3) the issuance of an order under section 514(b)(2) or 515 (b)(2)(B) denying a request for
reclassification of a device,
(4) the promulgation of a regulation under paragraph (3) of section 515(b) requiring a device to
have an approval of a premarket application, a regulation under paragraph (4) of that section
amending or revoking a regulation under paragraph (3), or an order pursuant to section
515(g)(1) or 515(g)(2)(C),
(5) the promulgation of a regulation under section 516 (other than a proposed regulation made
effective under subsection (b) of such section upon the regulation’s publication) making a
device a banned device,
(6) the issuance of an order under section 520(f)(2),
(7) an order under section 520(g)(4) disapproving an application for an exemption of a device
for investigational use or an order under section 520(g)(5) withdrawing such an exemption for
a device,
(8) an order pursuant to section 513(i), or
(9) a regulation under section 515(i)(2) or 520(l)(5)(B),
any person adversely affected by such regulation or order may file a petition with the United
States Court of Appeals for the District of Columbia or for the circuit wherein such person
resides or has his principal place of business for Judicial review of such regulation or order. A
copy of the petition shall be transmitted by the clerk of the court to the Secretary or other
officer designated by him for that purpose. The Secretary shall file in the court the record of the
proceedings on which the Secretary based his regulation or order as provided in section 2112
of title 28, United States Code. For purposes of this section, the term "record" means all
notices and other matter published in the Federal Register with respect to the regulation or
order reviewed, all information submitted to the Secretary with respect to such regulation or
order, proceedings of any panel or advisory committee with respect to such regulation or order,
any hearing held with respect to such regulation or order, and any other information identified
by the Secretary, in the administrative proceeding held with respect to such regulation or order,
as being relevant to such regulation or order.
(b) Additional Data, Views, and Arguments. If the petitioner applies to the court for leave to
adduce additional data, views, or arguments respecting the regulation or order being reviewed
and shows to the satisfaction of the court that such additional data, views, or arguments are
material and that there were reasonable grounds for the petitioner’s failure to adduce such
data, views, or arguments in the proceedings before the Secretary, the court may order the
Secretary to provide additional opportunity for the oral presentation of data, views, or
arguments and for written submissions. The Secretary may modify his findings, or make new
findings by reason of the additional data, views, or arguments so taken and shall file with the
court such modified or new findings, and his recommendation, if any, for the modification or
setting aside of the regulation or order being reviewed, with the return of such additional data,
views, or arguments.
(c) Standard for Review. Upon the filing of the petition under subsection (a) of this section for
judicial review of a regulation or order, the court shall have jurisdiction to review the regulation
or order in accordance with chapter 7 of title 5, United States Code, and to grant appropriate
relief, including interim relief, as provided in such chapter. A regulation described in paragraph
(2) or (5) of subsection (a) and an order issued after the review provided by section 515(g)
shall not be affirmed if it is found to be unsupported by substantial evidence on the record
taken as a whole.
(d) Finality of Judgments, The judgment of the court affirming or setting aside, in whole or in
part, any regulation or order shall be final, subject to review by the Supreme Court of the
United States upon certiorari or certification, as provided in section 1254 of title 28 of the
United States Code.
(e) Other Remedies. The remedies provided for in this section shall be in addition to and not in
lieu of any other remedies provided by law.
(f) Statement of Reasons. To facilitate judicial review under this section or under any other
provision of law of a regulation or order issued under section 513, 514, 515, 516, 518, 519,
520, or 521 each such regulation or order shall contain a statement of the reasons for its
issuance and the basis, in the record of the proceedings held in connection with its issuance,
for its issuance.
NOTIFICATION AND OTHER REMEDIES
SEC. 518. [21 U.S.C. 360h ] (a) Notification. If the Secretary determines that—
(1) a device intended for human use which is introduced or delivered for introduction into
interstate commerce for commercial distribution presents an unreasonable risk of substantial
harm to the public health, and
(2) notification under this subsection is necessary to eliminate the unreasonable risk of such
harm and no more practicable means is available under the provisions of this Act (other than
this section) to eliminate such risk,
the Secretary may issue such order as may be necessary to assure that adequate notification
is provided in an appropriate form, by the persons and means best suited under the
circumstances involved, to all health professionals who prescribe or use the device and to any
other person (including manufacturers, importers, distributors, retailers, and device users) who
should properly receive such notification in order to eliminate such risk. An order under this
subsection shall require that the individuals subject to the risk with respect to which the order is
to be issued be included in the persons to be notified of the risk unless the Secretary
determines that notice to such individuals would present a greater danger to the health of such
individuals than no such notification. If the Secretary makes such a determination with respect
to such individuals, the order shall require that the health professionals who prescribe or use
the device provide for the notification of the individuals whom the health professionals treated
with the device of the risk presented by the device and of any action which may be taken by or
on behalf of such individuals to eliminate or reduce such risk. Before issuing an order under
this subsection, the Secretary shall consult with the persons who are to give notice under the
order.
(b) Repair, Replacement, or Refund
(1)(A) If, after affording opportunity for an informal hearing, the Secretary determines that—
(i) a device intended for human use which is introduced or delivered for introduction into
interstate commerce for commercial distribution presents an unreasonable risk of substantial
harm to the public health.
(ii) there are reasonable grounds to believe that the device was not properly designed or
manufactured with reference to the state of the art as it existed at the time of its design or
manufacture,
(iii) there are reasonable grounds to believe that the unreasonable risk was not caused by
failure of a person other than a manufacturer, importer, distributor, or retailer of the device to
exercise due care in the installation, maintenance, repair, or use of the device, and
(iv) the notification authorized by subsection (a) would not by itself be sufficient to eliminate the
unreasonable risk and action described in paragraph (2) of this subsection is necessary to
eliminate such risk,
the Secretary may order the manufacturer, importer, or any distributor of such device, or any
combination of such persons, to submit to him within a reasonable time a plan for taking one or
more of the actions described in paragraph (2). An order issued under the preceding sentence
which is directed to more than one person shall specify which person may decide which action
shall be taken under such plan and the person specified shall be the person who the Secretary
determines bears the principal, ultimate financial responsibility for action taken under the plan
unless the Secretary cannot determine who bears such responsibility or the Secretary
determines that the protection of the public health requires that such decision be made by a
person (including a device user or health professional) other than the person he determines
bears such responsibility.
(B) The Secretary shall approve a plan submitted pursuant to an order issued under
subparagraph (A) unless he determines (after affording opportunity for an informal hearing)
that the action or actions to be taken under the plan or the manner in which such action or
actions are to be taken under the plan will not assure that the unreasonable risk with respect to
which such order was issued will be eliminated. If the Secretary disapproves a plan, he shall
order a revised plan to be submitted to him within a reasonable time. If the Secretary
determines (after affording opportunity for an informal hearing) that the revised plan is
unsatisfactory or if no revised plan or no initial plan has been submitted to the Secretary within
the prescribed time, the Secretary shall (i) prescribe a plan to be carried out by the person or
persons to whom the order issued under subparagraph (A) was directed, or (ii) after affording
an opportunity for an informal hearing, by order prescribe a plan to be carried out by a person
who is a manufacturer, importer, distributor, or retailer of the device with respect to which the
order was issued but to whom the order under subparagraph (A) was not directed.
(2) The actions which may be taken under a plan submitted under an order issued under
paragraph (1) are as follows:
(A) To repair the device so that it does not present the unreasonable risk of substantial harm
with respect to which the order under paragraph (1) was issued.
(B) To replace the device with a like or equivalent device which is in conformity with all
applicable requirements of this Act.
(C) To refund the purchase price of the device (less a reasonable allowance for use if such
device has been in the possession of the device user for one year or more—
(i) at the time of notification ordered under subsection (a), or
(ii) at the time the device user receives actual notice of the unreasonable risk with respect to
which the order was issued under paragraph (1), whichever first occurs).
(3) No charge shall be made to any person (other than a manufacturer, importer, distributor or
retailer) for availing himself of any remedy, described in paragraph (2) and provided under an
order issued under paragraph (1), and the person subject to the order shall reimburse each
person (other than a manufacturer, importer, distributor, or retailer) who is entitled to such a
remedy for any reasonable and foreseeable expenses actually incurred by such person in
availing himself of such remedy.
(c) Reimbursement. An order issued under subsection (b) with respect to a device may require
any person who is a manufacturer, importer, distributor, or retailer of the device to reimburse
any other person who is a manufacturer, importer, distributor, or retailer of such device for
such other person’s expenses actually incurred in connection with carrying out the order if the
Secretary determines such reimbursement is required for the protection of the public health.
Any such requirement shall not affect any rights or obligations under any contract to which the
person receiving reimbursement or the person making such reimbursement is a party.
(d) Effect on Other Liability. Compliance with an order issued under this section shall not
relieve any person from liability under Federal or State law. In awarding damages for economic
loss in an action brought for the enforcement of any such liability, the value to the plaintiff in
such action of any remedy provided him under such order shall be taken into account.
(e) Recall Authority
(1) If the Secretary finds that there is a reasonable probability that a device intended for human
use would cause serious, adverse health consequences or death, the Secretary shall issue an
order requiring the appropriate person (including the manufacturers, importers, distributors, or
retailers of the device)—
(A) to immediately cease distribution of such device, and
(B) to immediately notify health professionals and device user facilities of the order and to
instruct such professionals and facilities to cease use of such device.
The order shall provide the person subject to the order with an opportunity for an informal
hearing, to be held not later than 10 days after the date of the issuance of the order, on the
actions required by the order and on whether the order should be amended to require a recall
of such device. If, after providing an opportunity for such a hearing, the Secretary determines
that inadequate grounds exist to support the actions required by the order, the Secretary shall
vacate the order.
(2)(A) If, after providing an opportunity for an informal hearing under paragraph (1), the
Secretary determines that the order should be amended to include a recall of the device with
respect to which the order was issued, the Secretary shall, except as provided in
subparagraphs (B) and (C), amend the order to require a recall. The Secretary shall specify a
timetable in which the device recall will occur and shall require periodic reports to the
Secretary describing the progress of the recall.
(B) An amended order under subparagraph (A)—
(i) shall—
(I) not include recall of a device from individuals, and
(II) not include recall of a device from device user facilities if the Secretary determines that the
risk of recalling such device from the facilities presents a greater health risk than the health risk
of not recalling the device from use, and
(ii) shall provide for notice to individuals subject to the risks associated with the use of such
device.
In providing the notice required by clause (ii), the Secretary may use the assistance of health
professionals who prescribed or used such a device for individuals. If a significant number of
such individuals cannot be identified, the Secretary shall notify such individuals pursuant to
section 705(b).
(3) The remedy provided by this subsection shall be in addition to remedies provided by
subsections (a), (b), and (c).
RECORDS AND REPORTS ON DEVICES
SEC. 519. [21 U.S.C. 360i ] (a) General Rule. Every person who is a manufacturer or importer
of a device intended for human use shall establish and maintain such records, make such
reports, and provide such information, as the Secretary may by regulation reasonably require
to assure that such device is not adulterated or misbranded and to otherwise assure its safety
and effectiveness. Regulations prescribed under the preceding sentence—
(1) shall require a device manufacturer or importer to report to the Secretary whenever the
manufacturer or importer receives or otherwise becomes aware of information that reasonably
suggests that one of its marketed devices—
(A) may have caused or contributed to a death or serious injury, or
(B) has malfunctioned and that such device or a similar device marketed by the manufacturer
or importer would be likely to cause or contribute to a death or serious injury if the malfunction
were to recur;
(2) shall define the term "serious injury" to mean an injury that—
(A) is life threatening,
(B) results in permanent impairment of a body function or permanent damage to a body
structure, or
(C) necessitates medical or surgical intervention to preclude permanent impairment of a body
function or permanent damage to a body structure;
(3) shall require reporting of other significant adverse device experiences as determined by the
Secretary to be necessary to be reported;
(4) shall not impose requirements unduly burdensome to a device manufacturer or importer
taking into account his cost of complying with such requirements and the need for the
protection of the public health and the implementation of this Act;
(5) which prescribe the procedure for making requests for reports or information shall require
that each request made under such regulations for submission of a report or information to the
Secretary state the reason or purpose for such request and identify to the fullest extent
practicable such report or information;
(6) which require submission of a report or information to the Secretary shall state the reason
or purpose for the submission of such report or information and identify to the fullest extent
practicable such report or information;
(7) may not require that the identity of any patient be disclosed in records, reports, or
information required under this subsection unless required for the medical welfare of an
individual, to determine the safety or effectiveness of a device, or to verify a record, report, or
information submitted under this Act; and
(8) may not require a manufacturer or importer of a class I device to—
(A) maintain for such a device records respecting information not in the possession of the
manufacturer or importer, or
(B) to submit for such a device to the Secretary any report or information—
(i) not in the possession of the manufacturer or importer, or
(ii) on a periodic basis,
unless such report or information is necessary to determine if the device should be reclassified
or if the device is adulterated or misbranded. and 3
In prescribing such regulations, the Secretary shall have due regard for the professional ethics
of the medical profession and the interests of patients. The prohibitions of paragraph (7) of this
subsection continue to apply to records, reports, and information concerning any individual
who has been a patient, irrespective of whether or when he ceases to be a patient. The
Secretary shall by regulation require distributors to keep records and make such records
available to the Secretary upon request. Paragraphs (4) and (8) apply to distributors to the
same extent and in the same manner as such paragraphs apply to manufacturers and
importers.
(b) User Reports
(1)(A) Whenever a device user facility receives or otherwise becomes aware of information
that reasonably suggests that a device has or may have caused or contributed to the death of
a patient of the facility, the facility shall, as soon as practicable but not later than 10 working
days after becoming aware of the information, report the information to the Secretary and, if
the identity of the manufacturer is known, to the manufacturer of the device. In the case of
deaths, the Secretary may by regulation prescribe a shorter period for the reporting of such
information.
(B) Whenever a device user facility receives or otherwise becomes aware of—
(i) information that reasonably suggests that a device has or may have caused or contributed
to the serious illness of, or serious injury to, a patient of the facility, or
(ii) other significant adverse device experiences as determined by the Secretary by regulation
to be necessary to be reported,
shall, as soon as practicable but not later than 10 working days after becoming aware of the
information, report the information to the manufacturer of the device or to the Secretary if the
identity of the manufacturer is not known.
(C) Each device user facility shall submit to the Secretary on an annual basis a summary of the
reports made under subparagraphs (A) and (B). Such summary shall be submitted on January
1 of each year. The summary shall be in such form and contain such information from such
reports as the Secretary may require and shall include—
(i) sufficient information to identify the facility which made the reports for which the summary is
submitted,
(ii) in the case of any product which was the subject of a report, the product name, serial
number, and model number,
(iii) the name and the address of the manufacturer of such device, and
(iv) a brief description of the event reported to the manufacturer.
(D) For purposes of subparagraphs (A), (B), and (C), a device user facility shall be treated as
having received or otherwise become aware of information with respect to a device of that
facility when medical personnel who are employed by or otherwise formally affiliated with the
facility receive or otherwise become aware of information with respect to that device in the
course of their duties.
(2) The Secretary may not disclose the identity of a device user facility which makes a report
under paragraph (1) except in connection with—
(A) an action brought to enforce section 301(q), or
(B) a communication to a manufacturer of a device which is the subject of a report under
paragraph (1).
This paragraph does not prohibit the Secretary from disclosing the identity of a device user
facility making a report under paragraph (1) or any information in such a report to employees of
the Department of Health and Human Services, to the Department of Justice, or to the duly
authorized committees and subcommittees of the Congress.
(3) No report made under paragraph (1) by—
(A) a device user facility,
(B) an individual who is employed by or otherwise formally affiliated with such a facility, or
(C) a physician who is not required to make such a report,
shall be admissible into evidence or otherwise used in any civil action involving private parties
unless the facility, individual, or physician who made the report had knowledge of the falsity of
the information contained in the report.
(4) A report made under paragraph (1) does not affect any obligation of a manufacturer who
receives the report to file a report as required under subsection (a).
(5) With respect to device user facilities:
(A) The Secretary shall by regulation plan and implement a program under which the
Secretary limits user reporting under paragraphs (1) through (4) to a subset of user facilities
that constitutes a representative profile of user reports for device deaths and serious illnesses
or serious injuries.
(B) During the period of planning the program under subparagraph (A), paragraphs (1) through
(4) continue to apply.
(C) During the period in which the Secretary is providing for a transition to the full
implementation of the program, paragraphs (1) through (4) apply except to the extent that the
Secretary determines otherwise.
(D) On and after the date on which the program is fully implemented, paragraphs (1) through
(4) do not apply to a user facility unless the facility is included in the subset referred to in
subparagraph (A).
(E) Not later than 2 years after the date of the enactment of the Food and Drug Administration
Modernization Act of1997, the Secretary shall submit to the Committee on Commerce of the
House of Representatives, and to the Committee on Labor and Human Resources of the
Senate, a report describing the plan developed by the Secretary under subparagraph (A) and
the progress that has been made toward the implementation of the plan.
(6) For purposes of this subsection:
(A) The term "device user facility" means a hospital, ambulatory surgical facility, nursing home,
or outpatient treatment facility which is not a physician’s office. The Secretary may by
regulation include an outpatient diagnostic facility which is not a physician’s office in such term.
(B) The terms "serious illness" and "serious injury" mean illness or injury, respectively, that—
(i) is life threatening,
(ii) results in permanent impairment of a body function or permanent damage to a body stru(iii)
necessitates medical or surgical intervention to preclude permanent impairment of a body
function or permanent damage to a body structure.cture, or
(c) Persons Exempt. Subsection (a) shall not apply to—
(1) any practitioner who is licensed by law to prescribe or administer devices intended for use
in humans and who manufactures or imports devices solely for use in the course of his
professional practice;
(2) any person who manufactures or imports devices intended for use in humans solely for
such person’s use in research or teaching and not for sale (including any person who uses a
device under an exemption granted under section 520(g)); and
(3) any other class of persons as the Secretary may by regulation exempt from subsection (a)
upon a finding that compliance with the requirements of such subsection by such class with
respect to a device is not necessary to (A) assure that a device is not adulterated or
misbranded or (B) otherwise to assure its safety and effectiveness.
[(d) Repealed by Pub. L. 105–115, November 21, 1997. ]
(e) Device Tracking
(1) The Secretary may by order require a manufacturer to
(A) the failure of which would be reasonably likely to have serious adverse health
consequences; or
(B) which is—
(i) intended to be implanted in the human body for more than one year, or
(ii) a life sustaining or life supporting device used outside a device user facility.
(2) Any patient receiving a device subject to tracking under paragraph (1) may refuse to
release, or refuse permission to release, the patient’s name, address, social security number,
or other identifying information for the purpose of tracking.
(f) Reports of Removals and Corrections
(1) Except as provided in paragraph (2), the Secretary shall by regulation require a
manufacturer or importer of a device to report promptly to the Secretary any correction or
removal of a device undertaken by such manufacturer or importer if the removal or correction
was undertaken—
(A) to reduce a risk to health posed by the device, or
(B) to remedy a violation of this Act caused by the device which may present a risk to health.
A manufacturer or importer of a device who undertakes a correction or removal of a device
which is not required to be reported under this paragraph shall keep a record of such
correction or removal.
(2) No report of the corrective action or removal of a device may be required under paragraph
(1) if a report of the corrective action or removal is required and has been submitted under
subsection (a).
(3) For purposes of paragraphs (1) and (2), the terms "correction" and "removal" do not include
routine servicing.
GENERAL PROVISIONS RESPECTING CONTROL OF DEVICES INTENDED FOR HUMAN
USE
SEC. 520. [21 USC 360j ] (a) General rule. Any requirement authorized by or under section
501, 502, 510, or 519 applicable to a device intended for human use shall apply to such device
until the applicability of the requirement to the device has been changed by action taken under
section 513, 514, or 515 or under subsection (g) of this section, and any requirement
established by or under section 501, 502, 510, or 519 which is inconsistent with a requirement
imposed on such device under section 514 or 515 or under subsection (g) of this section shall
not apply to such device.
(b) Custom devices. Sections 514 and 515 do not apply to any device which, in order to
comply with the order of an individual physician or dentist (or any other specially qualified
person designated under regulations promulgated by the Secretary after an opportunity for an
oral hearing) necessarily deviates from an otherwise applicable performance standard or
requirement prescribed by or under section 515 if
(1) the device is not generally available in finished form for purchase or for dispensing upon
prescription and is not offered through labeling or advertising by the manufacturer, importer, or
distributor thereof for commercial distribution, and
(2) such device
(A)(i) is intended for use by an individual patient named in such order of such physician or
dentist (or other specially qualified person so designated) and is to be made in a specific form
for such patient, or
(ii) is intended to meet the special needs of such physician or dentist (or other specially
qualified person so designated) in the course of the professional practice of such physician or
dentist (or other specially qualified person so designated), and
(B) is not generally available to or generally used by other physicians or dentists (or other
specially qualified persons so designated).
(c) Trade secrets. Any information reported to or otherwise obtained by the Secretary or his
representative under section 513, 514, 515, 516, 518, 519, or 704 or under subsection (f) or (g)
of this section which is exempt from disclosure pursuant to subsection (a) of section 552 of title
5, United States Code, by reason of subsection (b)(4) of such section shall be considered
confidential and shall not be disclosed and may not be used by the Secretary as the basis for
the reclassification of a device from class III to class II or class I or as the basis for the
establishment or amendment of a performance standard under section 514 for a device
reclassified from class III to class II, except (1) in accordance with subsection (h), and (2) that
such information may be disclosed to other officers or employees concerned with carrying out
this Act or when relevant in any proceeding under this Act (other than section 513 or 514
thereof).
(d) Notices and findings. Each notice of proposed rulemaking under section 513, 514, 515, 516,
518, or 519, or under this section, any other notice which is published in the Federal Register
with respect to any other action taken under any such section and which states the reasons for
such action, and each publication of findings required to be made in connection with
rulemaking under any such section shall set forth
(1) the manner in which interested persons may examine data and other information on which
the notice or findings is based, and
(2) the period within which interested persons may present their comments on the notice or
findings (including the need therefor) orally or in writing, which period shall be at least sixty
days but may not exceed ninety days unless the time is extended by the Secretary by a notice
published in the Federal Register stating good cause therefor.
(e) Restricted devices.
(1) The Secretary may by regulation require that a device be restricted to sale, distribution, or
use
(A) only upon the written or oral authorization of a practitioner licensed by law to administer or
use such device, or
(B) upon such other conditions as the Secretary may prescribe in such regulation,
if, because of its potentiality for harmful effect or the collateral measures necessary to its use,
the Secretary determines that there cannot otherwise be reasonable assurance of its safety
and effectiveness. No condition prescribed under subparagraph (B) may restrict the use of a
device to persons with specific training or experience in its use or to persons for use in certain
facilities unless the Secretary determines that such a restriction is required for the safe and
effective use of the device. No such condition may exclude a person from using a device solely
because the person does not have the training or experience to make him eligible for
certification by a certifying board recognized by the American Board of Medical Specialties or
has not been certified by such a Board. A device subject to a regulation under this subsection
is a restricted device.
(2) The label of a restricted device shall bear such appropriate statements of the restrictions
required by a regulation under paragraph (1) as the Secretary may in such regulation
prescribe.
(f) Good manufacturing practice requirements.
(1)(A) The Secretary may, in accordance with subparagraph (B), prescribe regulations
requiring that the methods used in, and the facilities and controls used for, the manufacture,
pre-production design validation (including a process to assess the performance of a device
but not including an evaluation of the safety or effectiveness of a device), packing, storage,
and installation of a device conform to current good manufacturing practice, as prescribed in
such regulations, to assure that the device will be safe and effective and otherwise in
compliance with this Act.
(B) Before the Secretary may promulgate any regulation under subparagraph (A) he shall
(i) afford the advisory committee established under paragraph (3) an opportunity to submit
recommendations to him with respect to the regulation proposed to be promulgated;
(ii) afford opportunity for an oral hearing; and
(iii) ensure that such regulation conforms, to the extent practicable, with internationally
recognized standards defining quality systems, or parts of the standards, for medical devices.
The Secretary shall provide the advisory committee a reasonable time to make its
recommendation with respect to proposed regulations under subparagraph (A).
(2)(A) Any person subject to any requirement prescribed by regulations under paragraph (1)
may petition the Secretary for an exemption or variance from such requirement. Such a
petition shall be submitted to the Secretary in such form and manner as he shall prescribe and
shall—
(i) in the case of a petition for an exemption from a requirement, set forth the basis for the
petitioner’s determination that compliance with the requirement is not required to assure that
the device will be safe and effective and otherwise in compliance with this Act,
(ii) in the case of a petition for a variance from a requirement, set forth the methods proposed
to be used in, and the facilities and controls proposed to be used for, the manufacture, packing,
storage, and installation of the device in lieu of the methods, facilities, and controls prescribed
by the requirement, and
(iii) contain such other information as the Secretary shall prescribe.
(B) The Secretary may refer to the advisory committee established under paragraph (3) any
petition submitted under subparagraph (A). The advisory committee shall report its
recommendations to the Secretary with respect to a petition referred to it within sixty days of
the date of the petition’s referral. Within sixty days after
(i) the date the petition was submitted to the Secretary under subparagraph (A), or
(ii) if the petition was referred to an advisory committee, the expiration of the sixty-day period
beginning on the date the petition was referred to the advisory committee,
whichever occurs later, the Secretary shall by order either deny the petition or approve it.
(C) The Secretary may approve
(i) a petition for an exemption for a device from a requirement if he determines that compliance
with such requirement is not required to assure that the device will be safe and effective and
otherwise in compliance with this Act, and
(ii) a petition for a variance for a device from a requirement if he determines that the methods
to be used in, and the facilities and controls to be used for, the manufacture, packing, storage,
and installation of the device in lieu of the methods, controls, and facilities prescribed by the
requirement are sufficient to assure that the device will be safe and effective and otherwise in
compliance with this Act.
An order of the Secretary approving a petition for a variance shall prescribe such conditions
respecting the methods used in, and the facilities and controls used for, the manufacture,
packing, storage, and installation of the device to be granted the variance under the petition as
may be necessary to assure that the device will be safe and effective and otherwise in
compliance with this Act.
(D) After the issuance of an order under subparagraph (B) respecting a petition, the petitioner
shall have an opportunity for an informal hearing on such order.
(3) The Secretary shall establish an advisory committee for the purpose of advising and
making recommendations to him with respect to regulations proposed to be promulgated
under paragraph (1)(A) and the approval or disapproval of petitions submitted under
paragraph (2). The advisory committee shall be composed of nine members as follows:
(A) Three of the members shall be appointed from persons who are officers or employees of
any State or local government or of the Federal Government.
(B) Two of the members shall be appointed from persons who are representative of interests
of the device manufacturing industry; two of the members shall be appointed from persons
who are representative of the interests of physicians and other health professionals; and two of
the members shall be representative of the interests of the general public.
Members of the advisory committee who are not officers or employees of the United States,
while attending conferences or meetings of the committee or otherwise engaged in its
business, shall be entitled to receive compensation at rates to be fixed by the Secretary, which
rates may not exceed the daily equivalent of the rate in effect for grade GS-18 of the General
Schedule 4 , for each day (including travel time) they are so engaged; and while so serving
away from their homes or regular places of business each member may be allowed travel
expenses, including per diem in lieu of subsistence, as authorized by section 5703 of title 5 of
the United States Code for persons in the Government service employed intermittently. The
Secretary shall designate one of the members of the advisory committee to serve as its
chairman. The Secretary shall furnish the advisory committee with clerical and other
assistance. Section 14 of the Federal Advisory Committee Act shall not apply with respect to
the duration of the advisory committee established under this paragraph.
(g) Exemption for devices for investigational use.
(1) It is the purpose of this subsection to encourage, to the extent consistent with the protection
of the public health and safety and with ethical standards, the discovery and development of
useful devices intended for human use and to that end to maintain optimum freedom for
scientific investigators in their pursuit of that purpose.
(2)(A) The Secretary shall, within the one hundred and twenty day period beginning on the
date of the enactment of this section [enacted May 28, 1976], by regulation prescribe
procedures and conditions under which devices intended for human use may upon application
be granted an exemption from the requirements of section 502, 510, 514, 515, 516, 519, or
721 or subsection (e) or (f) of this section or from any combination of such requirements to
permit the investigational use of such devices by experts qualified by scientific training and
experience to investigate the safety and effectiveness of such devices.
(B) The conditions prescribed pursuant to subparagraph (A) shall include the following:
(i) A requirement that an application be submitted to the Secretary before an exemption may
be granted and that the application be submitted in such form and manner as the Secretary
shall specify.
(ii) A requirement that the person applying for an exemption for a device assure the
establishment and maintenance of such records, and the making of such reports to the
Secretary of data obtained as a result of the investigational use of the device during the
exemption, as the Secretary determines will enable him to assure compliance with such
conditions, review the progress of the investigation, and evaluate the safety and effectiveness
of the device.
(iii) Such other requirements as the Secretary may determine to be necessary for the
protection of the public health and safety.
(C) Procedures and conditions prescribed pursuant to subparagraph (A) for an exemption may
appropriately vary depending on (i) the scope and duration of clinical testing to be conducted
under such exemption, (ii) the number of human subjects that are to be involved in such
testing, (iii) the need to permit changes to be made in the device subject to the exemption
during testing conducted in accordance with a clinical testing plan required under paragraph
(3)(A), and (iv) whether the clinical testing of such device is for the purpose of developing data
to obtain approval for the commercial distribution of such device.
(3) Procedures and conditions prescribed pursuant to paragraph (2)(A) shall require, as a
condition to the exemption of any device to be the subject of testing involving human subjects,
that the person applying for the exemption
(A) submit a plan for any proposed clinical testing of the device and a report of prior
investigations of the device (including, where appropriate, tests on animals) adequate to justify
the proposed clinical testing
(i) to the local institutional review committee which has been established in accordance with
regulations of the Secretary to supervise clinical testing of devices in the facilities where the
proposed clinical testing is to be conducted, or
(ii) to the Secretary, if
(I) no such committee exists, or
(II) the Secretary finds that the process of review by such committee is inadequate (whether or
not the plan for such testing has been approved by such committee),
for review for adequacy to justify the commencement of such testing; and, unless the plan and
report are submitted to the Secretary, submit to the Secretary a summary of the plan and a
report of prior investigations of the device (including, where appropriate, tests on animals);
(B) promptly notify the Secretary (under such circumstances and in such manner as the
Secretary prescribes) of approval by a local institutional review committee of any clinical
testing plan submitted to it in accordance with subparagraph (A);
(C) in the case of a device to be distributed to investigators for testing, obtain signed
agreements from each of such investigators that any testing of the device involving human
subjects will be under such investigator’s supervision and in accordance with subparagraph (D)
and submit such agreements to the Secretary; and
(D) assure that informed consent will be obtained from each human subject (or his
representative) of proposed clinical testing involving such device, except where subject to
such conditions as the Secretary may prescribe, the investigator conducting or supervising the
proposed clinical testing of the device determines in writing that there exists a life threatening
situation involving the human subject of such testing which necessitates the use of such
device and it is not feasible to obtain informed consent from the subject and there is not
sufficient time to obtain such consent from his representative.
The determination required by subparagraph (D) shall be concurred in by a licensed physician
who is not involved in the testing of the human subject with respect to which such
determination is made unless immediate use of the device is required to save the life of the
human subject of such testing and there is not sufficient time to obtain such concurrence.
(4)(A) An application, submitted in accordance with the procedures prescribed by regulations
under paragraph (2), for an exemption for a device (other than an exemption from section 516)
shall be deemed approved on the thirtieth day after the submission of the application to the
Secretary unless on or before such day the Secretary by order disapproves the application and
notifies the applicant of the disapproval of the application.
(B) The Secretary may disapprove an application only if he finds that the investigation with
respect to which the application is submitted does not conform to procedures and conditions
prescribed under regulations under paragraph (2). Such a notification shall contain the order of
disapproval and a complete statement of the reasons for the Secretary’s disapproval of the
application and afford the applicant opportunity for an informal hearing on the disapproval
order.
(5) The Secretary may by order withdraw an exemption granted under this subsection for a
device if the Secretary determines that the conditions applicable to the device under this
subsection for such exemption are not met. Such an order may be issued only after
opportunity for an informal hearing, except that such an order may be issued before the
provision of an opportunity for an informal hearing if the Secretary determines that the
continuation of testing under the exemption with respect to which the order is to be issued will
result in an unreasonable risk to the public health.
(6)(A) Not later than 1 year after the date of the enactment of the Food and Drug
Administration Modernization Act of 1997 [enacted Nov. 21, 1997], the Secretary shall by
regulation establish, with respect to a device for which an exemption under this subsection is
in effect, procedures and conditions that, without requiring an additional approval of an
application for an exemption or the approval of a supplement to such an application, permit
(i) developmental changes in the device (including manufacturing changes) that do not
constitute a significant change in design or in basic principles of operation and that are made
in response to information gathered during the course of an investigation; and
(ii) changes or modifications to clinical protocols that do not affect
(I) the validity of data or information resulting from the completion of an approved protocol, or
the relationship of likely patient risk to benefit relied upon to approve a protocol;
(II) the scientific soundness of an investigational plan submitted under paragraph (3)(A); or
(III) the rights, safety, or welfare of the human subjects involved in the investigation.
(B) Regulations under subparagraph (A) shall provide that a change or modification described
in such subparagraph may be made if
(i) the sponsor of the investigation determines, on the basis of credible information (as defined
by the Secretary) that the applicable conditions under subparagraph (A) are met; and
(ii) the sponsor submits to the Secretary, not later than 5 days after making the change or
modification, a notice of the change or modification.
(7)(A) In the case of a person intending to investigate the safety or effectiveness of a class III
device or any implantable device, the Secretary shall ensure that the person has an
opportunity, prior to submitting an application to the Secretary or to an institutional review
committee, to submit to the Secretary, for review, an investigational plan (including a clinical
protocol). If the applicant submits a written request for a meeting with the Secretary regarding
such review, the Secretary shall, not later than 30 days after receiving the request, meet with
the applicant for the purpose of reaching agreement regarding the investigational plan
(including a clinical protocol). The written request shall include a detailed description of the
device, a detailed description of the proposed conditions of use of the device, a proposed plan
(including a clinical protocol) for determining whether there is a reasonable assurance of
effectiveness, and, if available, information regarding the expected performance from the
device.
(B) Any agreement regarding the parameters of an investigational plan (including a clinical
protocol) that is reached between the Secretary and a sponsor or applicant shall be reduced to
writing and made part of the administrative record by the Secretary. Any such agreement shall
not be changed, except
(i) with the written agreement of the sponsor or applicant; or
(ii) pursuant to a decision, made in accordance with subparagraph (C) by the director of the
office in which the device involved is reviewed, that a substantial scientific issue essential to
determining the safety or effectiveness of the device involved has been identified.
(C) A decision under subparagraph (B)(ii) by the director shall be in writing, and may be made
only after the Secretary has provided to the sponsor or applicant an opportunity for a meeting
at which the director and the sponsor or applicant are present and at which the director
documents the scientific issue involved.
(h) Release of information respecting safety and effectiveness.
(1) The Secretary shall promulgate regulations under which a detailed summary of information
respecting the safety and effectiveness of a device which information was submitted to the
Secretary and which was the basis for
(A) an order under section 515(d)(1)(A) approving an application for premarket approval for
the device or denying approval of such an application or an order under section 515(e)
withdrawing approval of such an application for the device,
(B) an order under section 515(f)(6)(A) revoking an approved protocol for the device, an order
under section515(f)(6)(B) declaring a protocol for the device completed or not completed, or
an order under section 515(f)(7) revoking the approval of the device, or
(C) an order approving an application under subsection (g) for an exemption for the device
from section 516 or an order disapproving, or withdrawing approval of, an application for an
exemption under such subsection for the device,
shall be made available to the public upon issuance of the order. Summaries of information
made available pursuant to this paragraph respecting a device shall include information
respecting any adverse effects on health of the device.
(2) The Secretary shall promulgate regulations under which each advisory committee
established under section 515(g)(2)(B) shall make available to the public a detailed summary
of information respecting the safety and effectiveness of a device which information was
submitted to the advisory committee and which was the basis for its recommendation to the
Secretary made pursuant to section 515(g)(2)(A). A summary of information upon which such
a recommendation is based shall be made available pursuant to this paragraph only after the
issuance of the order with respect to which the recommendation was made and each summary
shall include information respecting any adverse effect on health of the device subject to such
order.
(3) Except as provided in paragraph (4), any information respecting a device which is made
available pursuant to paragraph (1) or (2) of this subsection (A) may not be used to establish
the safety or effectiveness of another device for purposes of this Act by any person other than
the person who submitted the information so made available, and (B) shall be made available
subject to subsection (c) of this section.
(4)(A) Any information contained in an application for Premarket approval filed with the
Secretary pursuant to section 515(c) (including information from clinical and preclinical tests or
studies that demonstrate the safety and effectiveness of a device, but excluding descriptions
of methods of manufacture and product composition and other trade secrets) shall be
available, 6 years after the application has been approved by the Secretary, for use by the
Secretary in
(i) approving another device;
(ii) determining whether a product development protocol has been completed, under section
515 for another device;
(iii) establishing a performance standard or special control under this Act; or
(iv) classifying or reclassifying another device under section 513 and subsection (l)(2).
(B) The publicly available detailed summaries of information respecting the safety and
effectiveness of devices required by paragraph (1)(A) shall be available for use by the
Secretary as the evidentiary basis for the agency actions described in subparagraph (A).
(i) Proceedings of advisory panels and committees. Each panel under section 513 and each
advisory committee established under section 514(b)(5)(B) or 515(g) or under subsection (f) of
this section shall make and maintain a transcript of any proceeding of the panel or committee.
Each such panel and committee shall delete from any transcript made pursuant to this
subsection information which under subsection (c) of this section is to be considered
confidential.
(j) Traceability. Except as provided in section 519(e), no regulation under this Act may impose
on a type or class of device requirements for the traceability of such type or class of device
unless such requirements are necessary to assure the protection of the public health.
(k) Research and development. The Secretary may enter into contracts for research, testing,
and demonstrations respecting devices and may obtain devices for research, testing, and
demonstration purposes without regard to sections 3648 and 3709 of the Revised Statutes (31
U.S.C. 529, 41 U.S.C. 5) 5 .
(l) Transitional provisions for devices considered as new drugs.
(1) Any device intended for human use
(A) for which on the date of enactment of the Medical Device Amendments of 1976 [enacted
May 28, 1976] 6 (hereinafter in this subsection referred to as the "enactment date") an
approval of an application submitted under section 505(b) was in effect;
(B) for which such an application was filed on or before the enactment date [enacted May 28,
1976] and with respect to which application no order of approval or refusing to approve had
been issued on such date under subsection (c) or (d) of such section;
(C) for which on the enactment date [enacted May 28, 1976] an exemption under subsection (i)
of such section was in effect;
(D) which is within a type of device described in subparagraph (A), (B), or (C) and is
substantially equivalent to another device within that type;
(E) which the Secretary in a notice published in the Federal Register before the enactment
date [enacted May 28, 1976] has declared to be a new drug subject to section 505; or
(F) with respect to which on the enactment date [enacted May 28, 1976] an action is pending
in a United States court under section 302, 303, or 304 for an alleged violation of a provision of
section 301 which enforces a requirement of section 505 or for an alleged violation of section
505(a),
is classified in class III unless the Secretary in response to a petition submitted under
paragraph (2) has classified such device in class I or II.
(2) The Secretary may initiate the reclassification of a device classified into class III under
paragraph (1) of this subsection or the manufacturer or importer of a device classified under
paragraph (1) may petition the Secretary (in such form and manner as he shall prescribe) for
the issuance of an order classifying the device in class I or class II. Within thirty days of the
filing of such a petition, the Secretary shall notify the petitioner of any deficiencies in the
petition which prevent the Secretary from making a decision on the petition. Except as
provided in paragraph (3)(D)(ii), within one hundred and eighty days after the filing of a petition
under this paragraph, the Secretary shall, after consultation with the appropriate panel under
section 513, by order either deny the petition or order the classification, in accordance with the
criteria prescribed by section 513(a)(1)(A) or 513(a)(1)(B), of the device in class I or class II.
(3)(A) In the case of a device which is described in paragraph (1)(A) and which is in class III—
(i) such device shall on the enactment date [enacted May 28, 1976] be considered a device
with an approved application under section 515, and
(ii) the requirements applicable to such device before the enactment date [enacted May 28,
1976] under section 505 shall continue to apply to such device until changed by the Secretary
as authorized by this Act.
(B) In the case of a device which is described in paragraph (1)(B) and which is in class III, an
application for such device shall be considered as having been filed under section 515 on the
enactment date [enacted May 28, 1976]. The period in which the Secretary shall act on such
application in accordance with section 515(d)(1) shall be one hundred and eighty days from
the enactment date [enacted May 28, 1976] (or such greater period as the Secretary and the
applicant may agree upon after the Secretary has made the finding required by section
515(d)(1)(B)(i)) less the number of days in the period beginning on the date an application for
such device was filed under section 505 and ending on the enactment date [enacted May 28,
1976]. After the expiration of such period such device is required, unless exempt under
subsection (g), to have in effect an approved application under section 515.
(C) A device which is described in paragraph (1)(C) and which is in class III shall be
considered a new drug until the expiration of the ninety-day period beginning on the date of the
promulgation of regulations under subsection (g) of this section. After the expiration of such
period such device is required, unless exempt under subsection (g), to have in effect an
approved application under section 515.
(D)(i) Except as provided in clauses (ii) and (iii), a device which is described in subparagraph
(D), (E), or (F) of paragraph (1) and which is in class III is required, unless exempt under
subsection (g) of this section, to have on and after sixty days after the enactment date
[enacted May 28, 1976] in effect an approved application under section 515.
(ii) If—
(I) a petition is filed under paragraph (2) for a device described in subparagraph (D), (E), or (F)
of paragraph (1), or
(II) an application for premarket approval is filed under section 515 for such a device,
within the sixty-day period beginning on the enactment date [enacted May 28, 1976] (or within
such greater period as the Secretary, after making the finding required under section
515(d)(1)(B), and the petitioner or applicant may agree upon), the Secretary shall act on such
petition or application in accordance with paragraph (2) or section 515 except that the period
within which the Secretary must act on the petition or application shall be within the one
hundred and twenty-day period beginning on the date the petition or application is filed. If such
a petition or application is filed within such sixty-day (or greater) period, clause (i) of this
subparagraph shall not apply to such device before the expiration of such one hundred and
twenty day period, or if such petition is denied or such application is denied approval, before
the date of such denial, whichever occurs first.
(iii) In the case of a device which is described in subparagraph (E) of paragraph (1), which the
Secretary in a notice published in the Federal Register after March 31, 1976, declared to be a
new drug subject to section 505, and which is in class III—
(I) the device shall, after eighteen months after the enactment date, have in effect an approved
application under section 515 unless exempt under subsection (g) of this section, and
(II) the Secretary may, during the period beginning one hundred and eighty days after the
enactment date [enacted May 28, 1976] and ending eighteen months after such date, restrict
the use of the device to investigational use by experts qualified by scientific training and
experience to investigate the safety and effectiveness of such device, and to investigational
use in accordance with the requirements applicable under regulations under subsection (g) of
this section to investigational use of devices granted an exemption under such subsection.
If the requirements under subsection (g) of this section are made applicable to the
investigational use of such a device, they shall be made applicable in such a manner that the
device shall be made reasonably available to physicians meeting appropriate qualifications
prescribed by the Secretary.
(4) [Deleted] [Repealed by Pub. L. 105–115, November 21, 1997. ]
(5)(A) Before December 1, 1991, the Secretary shall by order require manufacturers of
devices described in paragraph (1), which are subject to revision of classification under
subparagraph (B), to submit to the Secretary a summary of and citation to any information
known or otherwise available to the manufacturers respecting the devices, including adverse
safety or effectiveness information which has not been submitted under section 519. The
Secretary may require a manufacturer to submit the adverse safety or effectiveness data for
which a summary and citation were submitted, if such data are available to the manufacturer.
(B) Except as provided in subparagraph (C), after the issuance of an order under
subparagraph (A) but before December 1, 1992, the Secretary shall publish a regulation in the
Federal Register for each device which is classified in class III under paragraph (1) revising
the classification of the device so that the device is classified into class I or class II, unless the
regulation requires the device to remain in class III. In determining whether to revise the
classification of a device or to require a device to remain in class III, the Secretary shall apply
the criteria set forth in section 513(a). Before the publication of a regulation requiring a device
to remain in class III or revising its classification, the Secretary shall publish a proposed
regulation respecting the classification of a device under this subparagraph and provide an
opportunity for the submission of comments on any such regulation. No regulation under this
subparagraph requiring a device to remain in class III or revising its classification may take
effect before the expiration of 90 days from the date of the publication in the Federal Register
of the proposed regulation.
(C) The Secretary may by notice published in the Federal Register extend the period
prescribed by subparagraph (B) for a device for an additional period not to exceed 1 year.
(m) Humanitarian device exemption.
(1) To the extent consistent with the protection of the public health and safety and with ethical
standards, it is the purpose of this subsection to encourage the discovery and use of devices
intended to benefit patients in the treatment and diagnosis of diseases or conditions that affect
fewer than 4,000 individuals in the United States.
(2) The Secretary may grant a request for an exemption from the effectiveness requirements
of sections 514 and 515 for a device for which the Secretary finds that—
(A) the device is designed to treat or diagnose a disease or condition that affects fewer than
4,000 individuals in the United States,
(B) the device would not be available to a person with a disease or condition referred to in
subparagraph (A) unless the Secretary grants such an exemption and there is no comparable
device, other than under this exemption, available to treat or diagnose such disease or
condition, and
(C) the device will not expose patients to an unreasonable or significant risk of illness or injury
and the probable benefit to health from the use of the device outweighs the risk of injury or
illness from its use, taking into account the probable risks and benefits of currently available
devices or alternative forms of treatment.
The request shall be in the form of an application submitted to the Secretary. Not later than 75
days after the date of the receipt of the application, the Secretary shall issue an order
approving or denying the application.
(3) No person granted an exemption under paragraph (2) with respect to a device may sell the
device for an amount that exceeds the costs of research and development, fabrication, and
distribution of the device.
(4) Devices granted an exemption under paragraph (2) may only be used—
(A) in facilities that have established, in accordance with regulations of the Secretary, a local
institutional review committee to supervise clinical testing of devices in the facilities, and
(B) if, before the use of a device, an institutional review committee approves the use in the
treatment or diagnosis of a disease or condition referred to in paragraph (2)(A), unless a
physician determines in an emergency situation that approval from a local institutional review
committee can not be obtained in time to prevent serious harm or death to a patient.
In a case described in subparagraph (B) in which a physician uses a device without an
approval from an institutional review committee, the physician shall, after the use of the device,
notify the chairperson of the local institutional review committee of such use. Such notification
shall include the identification of the patient involved, the date on which the device was used,
and the reason for the use.
(5) The Secretary may require a person granted an exemption under paragraph (2) to
demonstrate continued compliance with the requirements of this subsection if the Secretary
believes such demonstration to be necessary to protect the public health or if the Secretary
has reason to believe that the criteria for the exemption are no longer met.
(6) The Secretary may suspend or withdraw an exemption from the effectiveness requirements
of sections 514 and 515 for a humanitarian device only after providing notice and an
opportunity for an informal hearing.
(n) Regulation of contact lens as devices.
(1) All contact lenses shall be deemed to be devices under section 201(h).
(2) Paragraph (1) shall not be construed as bearing on or being relevant to the question of
whether any product other than a contact lens is a device as defined by section 201(h) or a
drug as defined by section 201(g).
STATE AND LOCAL REQUIREMENTS RESPECTING DEVICES
SEC. 521. [21 U.S.C. 360k ] (a) General Rule. Except as provided in subsection (b), no State
or political subdivision of a State may establish or continue in effect with respect to a device
intended for human use any requirement—
(1) which is different from, or in addition to, any requirement applicable under this Act to the
device, and
(2) which relates to the safety or effectiveness of the device or to any other matter included in a
requirement applicable to the device under this Act.
(b) Exempt Requirements. Upon application of a State or a political subdivision thereof, the
Secretary may, by regulation promulgated after notice and opportunity for an oral hearing,
exempt from subsection (a), under such conditions as may be prescribed in such regulation, a
requirement of such State or political subdivision applicable to a device intended for human
use if—
(1) the requirement is more stringent than a requirement under this Act which would be
applicable to the device if an exemption were not in effect under this subsection; or
(2) the requirement—
(A) is required by compelling local conditions, and
(B) compliance with the requirement would not cause the device to be in violation of any
applicable requirement under this Act.
POSTMARKET SURVEILLANCE
SEC. 522. 7 [21 U.S.C. 360l ] (a) IN GENERAL.—The Secretary may by order require a
manufacturer to conduct postmarket surveillance for any device of the manufacturer which is a
class II or class III device the failure of which would be reasonably likely to have serious
adverse health consequences or which is intended to be—
(1) implanted in the human body for more than one year, or
(2) a life sustaining or life supporting device used outside a device user facility.
(b) SURVEILLANCE APPROVAL.—Each manufacturer required to conduct a surveillance of a
device shall, within 30 days of receiving an order from the Secretary prescribing that the
manufacturer is required under this section to conduct such surveillance, submit, for the
approval of the Secretary, a plan for the required surveillance. The Secretary, within 60 days of
the receipt of such plan, shall determine if the person designated to conduct the surveillance
has appropriate qualifications and experience to undertake such surveillance and if the plan
will result in the collection of useful data that can reveal unforeseen adverse events or other
information necessary to protect the public health. The Secretary, in consultation with the
manufacturer, may by order require a prospective surveillance period of up to 36 months. Any
determination by the Secretary that a longer period is necessary shall be made by mutual
agreement between the Secretary and the manufacturer or, if no agreement can be reached,
after the completion of a dispute resolution process as described in section 562.
ACCREDITED PERSONS.
SEC. 523. [21 U.S.C. 360m] (a) IN GENERAL.—
(1) REVIEW AND CLASSIFICATION OF DEVICES.—Not later than 1 year after the date of
the enactment of the Food and Drug Administration Modernization Act of 1997, the Secretary
shall, subject to paragraph (3), accredit persons for the purpose of reviewing reports submitted
under section 510(k) and making recommendations to the Secretary regarding the initial
classification of devices under section 513(f)(1).
(2) REQUIREMENTS REGARDING REVIEW.—
(A) IN GENERAL.—In making a recommendation to the Secretary under paragraph (1), an
accredited person shall notify the Secretary in writing of the reasons for the recommendation.
(B) TIME PERIOD FOR REVIEW.—Not later than 30 days after the date on which the
Secretary is notified under subparagraph (A) by an accredited person with respect to a
recommendation of an initial classification of a device, the Secretary shall make a
determination with respect to the initial classification.
(C) SPECIAL RULE.—The Secretary may change the initial classification under section
513(f)(1) that is recommended under paragraph (1) by an accredited person, and in such case
shall provide to such person, and the person who submitted the report under section 510(k) for
the device, a statement explaining in detail the reasons for the change.
(3) CERTAIN DEVICES.—
(A) IN GENERAL.—An accredited person may not be used to perform a review of—
(i) a class III device;
(ii) a class II device which is intended to be permanently implantable or life sustaining or life
supporting; or
(iii) a class II device which requires clinical data in the report submitted under section 510(k)
for the device, except that the number of class II devices to which the Secretary applies this
clause for a year, less the number of such reports to which clauses (i) and (ii) apply, may not
exceed 6 percent of the number that is equal to the total number of reports submitted to the
Secretary under such section for such year less the number of such reports to which such
clauses apply for such year.
(B) ADJUSTMENT.—In determining for a year the ratio described in subparagraph (A)(iii), the
Secretary shall not include in the numerator class III devices that the Secretary reclassified
into class II, and the Secretary shall include in the denominator class II devices for which
reports under section 510(k) were not required to be submitted by reason of the operation of
section 510(m).
(b) ACCREDITATION.—
(1) PROGRAMS.—The Secretary shall provide for such accreditation through programs
administered by the Food and Drug Administration, other government agencies, or by other
qualified non government organizations.
(2) ACCREDITATION.—
(A) IN GENERAL.—Not later than 180 days after the date of the enactment of the Food and
Drug Administration Modernization Act of 1997, the Secretary shall establish and publish in the
Federal Register criteria to accredit or deny accreditation to persons who request to perform
the duties specified in subsection (a). The Secretary shall respond to a request for
accreditation within 60 days of the receipt of the request. The accreditation of such person
shall specify the particular activities under subsection (a) for which such person is accredited.
(B) WITHDRAWAL OF ACCREDITATION.—The Secretary may suspend or withdraw
accreditation of any person accredited under this paragraph, after providing notice and an
opportunity for an informal hearing, when such person is substantially not in compliance with
the requirements of this section or poses a threat to public health or fails to act in a manner
that is consistent with the purposes of this section.
(C) PERFORMANCE AUDITING.—To ensure that persons accredited under this section will
continue to meet the standards of accreditation, the Secretary shall—
(i) make onsite visits on a periodic basis to each accredited person to audit the performance of
such person; and
(ii) take such additional measures as the Secretary determines to be appropriate.
(D) ANNUAL REPORT.—The Secretary shall include in the annual report required under
section 903(g) the names of all accredited persons and the particular activities under
subsection (a) for which each such person is accredited and the name of each accredited
person whose accreditation has been withdrawn during the year.
(3) QUALIFICATIONS.—An accredited person shall, at a minimum, meet the following
requirements:
(A) Such person may not be an employee of the Federal Government.
(B) Such person shall be an independent organization which is not owned or controlled by a
manufacturer, supplier, or vendor of devices and which has no organizational, material, or
financial affiliation with such a manufacturer, supplier, or vendor.
(C) Such person shall be a legally constituted entity permitted to conduct the activities for
which it seeks accreditation.
(D) Such person shall not engage in the design, manufacture, promotion, or sale of devices.
(E) The operations of such person shall be in accordance with generally accepted professional
and ethical business practices and shall agree in writing that as a minimum it will—
(i) certify that reported information accurately reflects data reviewed;
(ii) limit work to that for which competence and capacity are available;
(iii) treat information received, records, reports, and recommendations as proprietary
information;
(iv) promptly respond and attempt to resolve complaints regarding its activities for which it is
accredited; and
(v) protect against the use, in carrying out subsection (a) with respect to a device, of any officer
or employee of the person who has a financial conflict of interest regarding the device, and
annually make available to the public disclosures of the extent to which the person, and the
officers and employees of the person, have maintained compliance with requirements under
this clause relating to financial conflicts of interest.
(4) SELECTION OF ACCREDITED PERSONS.—The Secretary shall provide each person
who chooses to use an accredited person to receive a section 510(k) report a panel of at least
two or more accredited persons from which the regulated person may select one for a specific
regulatory function.
(5) COMPENSATION OF ACCREDITED PERSONS.—Compensation for an accredited
person shall be determined by agreement between the accredited person and the person who
engages the services of the accredited person, and shall be paid by the person who engages
such services.
(c) DURATION.— The authority provided by this section terminates October 1, 2007.
(d) REPORT.--Not later than January 10, 2007, the Secretary shall conduct a study based on
the experience under the program under this section and submit to the Committee on Energy
and Commerce of the House of Representatives, and the Committee on Health, Education,
Labor, and Pensions of the Senate, a report describing the findings of the study. The
objectives of the study shall include determining--
(1) the number of devices reviewed under this section;
(2) the number of devices reviewed under this section that were ultimately cleared by the
Secretary;
(3) the number of devices reviewed under this section that were ultimately not cleared by the
Secretary;
(4) the average time period for a review under this section (including the time it takes for the
Secretary to review a recommendation of an accredited person under subsection (a) and
determine the initial device classification);
(5) the average time period identified in paragraph (4) compared to the average time period for
review of devices solely by the Secretary pursuant to section 510(k);
(6) if there is a difference in the average time period under paragraph (4) and the average time
period under paragraph (5), the reasons for such difference;
(7) whether the quality of reviews under this section for devices for which no guidance has
been issued is qualitatively inferior to reviews by the Secretary for devices for which no
guidance has been issued;
(8) whether the quality of reviews under this section of devices for which no guidance has been
issued is qualitatively inferior to reviews under this section of devices for which guidance has
been issued;
(9) whether this section has in any way jeopardized or improved the public health;
(10) any impact of this section on resources available to the Secretary to review reports under
section 510(k); and
(11) any suggestions for continuation, modification (including contraction or expansion of
device eligibility), or termination of this section that the Secretary determines to be appropriate.
Footnotes: Sections 513-523
1. The General Schedule under section 5332 of title 5, United States Code, no longer includes
the grade GS-18. The grades are GS-1 through GS-15.
2. The General Schedule under section 5332 of title 5, United States Code, no longer includes
the grade GS-18. The grades are GS-1 through GS-15.
3. So in law. See section 213(a)(1)(D)(ii) of Public Law 105–115 (111 Stat. 2347). That section
struck former paragraph (9), and amended paragraph (8) "by striking the semicolon at the end
and inserting a period", rather than by striking "; and"; and inserting a period.
4. The General Schedule under section 5332 of title 5, United States Code, no longer includes
the grade GS-18. The grades are GS-1 through GS-15.
5. Section 3648 of the Revised Statutes has been superseded by subsections (a) and (b) of
section 3324 of title 31, United States Code. See Public Law 97–258.
6. Public Law 94–295, enacted May 28, 1976.
7. Section 212 of Public Law 107–250 (116 Stat. 1614), as amended by section 2(d)(3)(C) of
Public Law 108–214 (118 Stat. 577), provides for a study whose purpose is determining
whether the system under the Federal Food, Drug, and Cosmetic Act for the postmarket
surveillance of medical devices provides adequate safeguards regarding the use of devices in
pediatric populations. The study is required to be submitted not later than four years after the
date of the enactment of Public Law 107–250, which was enacted October 26, 2002.
CHAPTER V--DRUGS AND DEVICES
SUBCHAPTER B--DRUGS FOR RARE DISEASES OR CONDITIONS
RECOMMENDATIONS FOR INVESTIGATIONS OF DRUGS FOR RARE DISEASES OR
CONDITIONS 1
SEC. 525 . [21 U.S.C. 360aa] (a) The sponsor of a drug for a disease or condition which is rare
in the States may request the Secretary to provide written recommendations for the nonclinical
and clinical investigations which must be conducted with the drug before—
(1) it may be approved for such disease or condition under section 505, or
(2) if the drug is a biological product, it may be licensed for such disease or condition under
section 351 of the Public Health Service Act.
If the Secretary has reason to believe that a drug for which a request is made under this
section is a drug for a disease or condition which is rare in the States, the Secretary shall
provide the person making the request written recommendations for the nonclinical and clinical
investigations which the Secretary believes, on the basis of information available to the
Secretary at the time of the request under this section, would be necessary for approval of
such drug for such disease or condition under section 505 or licensing of such drug for such
disease or condition under section 351 of the Public Health Service Act.
(b) The Secretary shall by regulation promulgate procedures for the implementation of
subsection (a).
DESIGNATION OF DRUGS FOR RARE DISEASES OR CONDITIONS
SEC. 526 . [21 U.S.C. 360bb] (a)(1) The manufacturer or the sponsor of a drug may request
the Secretary to designate the drug as a drug for a rare disease or condition. A request for
designation of a drug shall be made before the submission of an application under section
505(b) for the drug, or the submission of an application for licensing of the drug under section
351 of the Public Health Service Act. If the Secretary finds that a drug for which a request is
submitted under this subsection is being or will be investigated for a rare disease or condition
and—
(A) if an application for such drug is approved under section 505, or
(B) if a license for such drug is issued under section 351of the Public Health Service Act, the
approval, certification, or license would be for use for such disease or condition, the Secretary
shall designate the drug as a drug for such disease or condition. A request for a designation of
a drug under this subsection shall contain the consent of the applicant to notice being given by
the Secretary under subsection (b) respecting the designation of the drug.
(2) For purposes of paragraph (1), the term ‘‘rare disease or condition’’ means any disease or
condition which (A) affects less than 200,000 persons in the United States, or (B) affects more
than 200,000 in the United States and for which there is no reasonable expectation that the
cost of developing and making available in the United States a drug for such disease or
condition will be recovered from sales in the United States of such drug. Determinations under
the preceding sentence with respect to any drug shall be made on the basis of the facts and
circumstances as of the date the request for designation of the drug under this subsection is
made.
(b) A designation of a drug under subsection (a) shall be subject to the condition that—
(1) if an application was approved for the drug under section 505(b) or a license was issued for
the drug under section 351 of the Public Health Service Act, the manufacturer of the drug will
notify the Secretary of any discontinuance of the production of the drug at least one year
before discontinuance, and
(2) if an application has not been approved for the drug under section 505(b) or a license has
not been issued for the drug under section 351 of the Public Health Service Act and if
preclinical investigations or investigations under section 505(i) are being conducted with the
drug, the manufacturer or sponsor of the drug will notify the Secretary of any decision to
discontinue active pursuit of approval of an application under section 505(b) or approval of a
license under section 351 of the Public Health Service Act.
(c) Notice respecting the designation of a drug under subsection (a) shall be made available to
the public.
(d) The Secretary shall by regulation promulgate procedures for the implementation of
subsection (a).
PROTECTION FOR DRUGS FOR RARE DISEASES OR CONDITIONS
SEC. 527 . [21 U.S.C. 360cc] (a) Except as provided in subsection (b), if the Secretary—
(1) approves an application filed pursuant to section 505, or
(2) issues a license under section 351 of the Public Health Service Act for a drug designated
under section 526 for a rare disease or condition, the Secretary may not approve another
application under section 505 or issue another license under section 351 of the Public Health
Service Act for such drug for such disease or condition for a person who is not the holder of
such approved application, of or of such license until the expiration of seven years from the
date of the approval of the approved application, or the issuance of the license. Section
505(c)(2) does not apply to the refusal to approve an application under the preceding
sentence.
(b) If an application filed pursuant to section 505 is approved for a drug designated under
section 526 for a rare disease or condition or if a license is issued under section 351 of the
Public Health Service Act for such a drug, the Secretary may, during the seven year period
beginning on the date of the application approval or of the issuance of the license, approve
another application under section 505 or issue a license under section 351 of the Public Health
Service Act, for such drug for such disease or condition for a person who is not the holder of
such approved application or of such license if—
(1) the Secretary finds, after providing the holder notice and opportunity for the submission of
views, that in such period the holder of the approved application or of the license cannot
assure the availability of sufficient quantities of the drug to meet the needs of persons with the
disease or condition for which the drug was designated; or
(2) such holder provides the Secretary in writing the consent of such holder for the approval of
other applications or the issuance of other licenses before the expiration of such seven year
period.
OPEN PROTOCOLS FOR INVESTIGATIONS OF DRUGS FOR RARE DISEASES OR
CONDITIONS
SEC. 528 . [21 U.S.C. 360dd] If a drug is designated under section 526 as a drug for a rare
disease or condition and if notice of a claimed exemption under section 505(i) or regulations
issued thereunder is filed for such drug, the Secretary shall encourage the sponsor of such
drug to design protocols for clinical investigations of the drug which may be conducted under
the exemption to permit the addition to the investigations of persons with the disease or
condition who need the drug to treat the disease or condition and who cannot be satisfactorily
treated by available alternative drugs.
Footnotes: Chapter V, Subchapter B
1. Section 5 of the Orphan Drug Act (21 U.S.C. 360ee) (Public Law 97–414), which is included
in the appendix, establishes a program to make grants and enter into contracts regarding the
development of drugs for rare diseases and conditions. Authorizations of appropriations for
that program are currently provided through fiscal year 2006. See section 3 of Public Law
107–281 (116 Stat. 1993).
CHAPTER V--DRUGS AND DEVICES
SUBCHAPTER C—ELECTRONIC PRODUCT RADIATION CONTROL
DEFINITIONS
SEC. 531. [21 U.S.C. 360hh] As used in this subchapter—
(1) the term "electronic product radiation" means—
(A) any ionizing or non-ionizing electromagnetic or particulate radiation, or
(B) any sonic, infrasonic, or ultrasonic wave, which is emitted from an electronic product as the
result of the operation of an electronic circuit in such product;
(2) the term "electronic product" means (A) any manufactured or assembled product which,
when in operation, (i) contains or acts as part of an electronic circuit and (ii) emits (or in the
absence of effective shielding or other controls would emit) electronic product radiation, or (B)
any manufactured or assembled article which is intended for use as a component, part, or
accessory of a product described in clause (A) and which when in operation emits (or in the
absence of effective shielding or other controls would emit) such radiation;
(3) the term "manufacturer" means any person engaged in the business of manufacturing,
assembling, or importing of electronic products;
(4) the term "commerce" means (A) commerce between any place in any State and any place
outside thereof; and (B) commerce wholly within the District of Columbia; and
(5) the term "State" includes the District of Columbia, the Commonwealth of Puerto Rico, the
Northern Mariana Islands, the Virgin Islands, Guam, and American Samoa.
ELECTRONIC PRODUCT RADIATION CONTROL PROGRAM
SEC. 532. [21 U.S.C. 360ii] (a) The Secretary shall establish and carry out an electronic
product radiation control program designed to protect the public health and safety from
electronic product radiation. As a part of such program, he shall—
(1) pursuant to section 534, develop and administer performance standards for electronic
products;
(2) plan, conduct, coordinate, and support research, development, training, and operational
activities to minimize the emissions of and the exposure of people to, unnecessary electronic
product radiation;
(3) maintain liaison with and receive information from other Federal and State departments
and agencies with related interests, professional organizations, industry, industry and labor
associations, and other organizations on present and future potential electronic product
radiation;
(4) study and evaluate emissions of, and conditions of exposure to, electronic product
radiation and intense magnetic fields;
(5) develop, test, and evaluate the effectiveness of procedures and techniques for minimizing
exposure to electronic product radiation; and
(6) consult and maintain liaison with the Secretary of Commerce, the Secretary of Defense, the
Secretary of Labor, the Atomic Energy Commission, and other appropriate Federal
departments and agencies on (A) techniques, equipment, and programs for testing and
evaluating electronic product radiation, and (B) the development of performance standards
pursuant to section 534 to control such radiation emissions.
(b) In carrying out the purposes of subsection (a), the Secretary is authorized to—
(1)(A) collect and make available, through publications and other appropriate means, the
results of, and other information concerning, research and studies relating to the nature and
extent of the hazards and control of electronic product radiation; and (B) make such
recommendations relating to such hazards and control as he considers appropriate;
(2) make grants to public and private agencies, organizations, and institutions, and to
individuals for the purposes stated in paragraphs (2), (4), and (5) of subsection (a) of this
section;
(3) contract with public or private agencies, institutions, and organizations, and with individuals,
without regard to section 3324 of title 31, United States Code, and section 3709 of the Revised
Statutes of the United States (41 U.S.C. 5); and
(4) procure (by negotiation or otherwise) electronic products for research and testing purposes,
and sell or otherwise dispose of such products.
(c)(1) Each recipient of assistance under this subchapter pursuant to grants or contracts
entered into under other than competitive bidding procedures shall keep such records as the
Secretary shall prescribe, including records which fully disclose the amount and disposition by
such recipient of the proceeds of such assistance, the total cost of the project or undertaking in
connection with which such assistance is given or used, and the amount of that portion of the
cost of the project or undertaking supplied by other sources, and such other records as will
facilitate an effective audit.
(2) The Secretary and the Comptroller General of the United States, or any of their duly
authorized representatives, shall have access for the purpose of audit and examination to any
books, documents, papers, and records of the recipient that are pertinent to the grants or
contracts entered into under this subchapter under other than competitive bidding procedures.
STUDIES BY THE SECRETARY
SEC. 533. [21 U.S.C. 360jj] (a) The Secretary shall conduct the following studies, and shall
make a report or reports of the results of such studies to the Congress on or before January 1,
1970, and from time to time thereafter as he may find necessary, together with such
recommendations for legislation as he may deem appropriate:
(1) A study of present State and Federal control of health hazards from electronic product
radiation and other types of ionizing radiation, which study shall include, but not be limited to—
(A) control of health hazards from radioactive materials other than materials regulated under
the Atomic Energy Act of 1954;
(B) any gaps and inconsistencies in present controls;
(C) the need for controlling the sale of certain used electronic products, particularly antiquated
X-ray equipment, without upgrading such products to meet the standards for new products or
separate standards for used products;
(D) measures to assure consistent and effective control of the aforementioned health hazards;
(E) measures to strengthen radiological health programs of State governments; and
(F) the feasibility of authorizing the Secretary to enter into arrangements with individual States
or groups of States to define their respective functions and responsibilities for the control of
electronic product radiation and other ionizing radiation;
(2) A study to determine the necessity for the development of standards for the use of
nonmedical electronic products for commercial and industrial purposes; and
(3) A study of the development of practicable procedures for the detection and measurement
of electronic product radiation which may be emitted from electronic products manufactured or
imported prior to the effective date of any applicable standard established pursuant to this
subchapter.
(b) In carrying out these studies, the Secretary shall invite the participation of other Federal
departments and agencies having related responsibilities and interests, State
governments—particularly those of States which regulate radioactive materials under section
274 of the Atomic Energy Act of 1954, as amended, and interested professional, labor, and
industrial organizations. Upon request from congressional committees interested in these
studies, the Secretary shall keep these committees currently informed as to the progress of the
studies and shall permit the committees to send observers to meetings of the study groups.
(c) The Secretary or his designee shall organize the studies and the participation of the invited
participants as he deems best. Any dissent from the findings and recommendations of the
Secretary shall be included in the report if so requested by the dissenter.
PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS
SEC. 534. [21 U.S.C. 360kk] (a)(1) The Secretary shall by regulation prescribe performance
standards for electronic products to control the emission of electronic product radiation from
such products if he determines that such standards are necessary for the protection of the
public health and safety. Such standards may include provisions for the testing of such
products and the measurement of their electronic product radiation emissions, may require the
attachment of warning signs and labels, and may require the provision of instructions for the
installation, operation, and use of such products. Such standards may be prescribed from time
to time whenever such determinations are made, but the first of such standards shall be
prescribed prior to January 1, 1970. In the development of such standards, the Secretary shall
consult with Federal and State departments and agencies having related responsibilities or
interests and with appropriate professional organizations and interested persons, including
representatives of industries and labor organizations which would be affected by such
standards, and shall give consideration to—
(A) the latest available scientific and medical data in the field of electronic product radiation;
(B) the standards currently recommended by (i) other Federal agencies having responsibilities
relating to the control and measurement of electronic product radiation, and (ii) public or
private groups having an expertise in the field of electronic product radiation;
(C) the reasonableness and technical feasibility of such standards as applied to a particular
electronic product;
(D) the adaptability of such standards to the need for uniformity and reliability of testing and
measuring procedures and equipment; and
(E) in the case of a component, or accessory described in paragraph (2)(B) of section 531, the
performance of such article in the manufactured or assembled product for which it is designed.
(2) The Secretary may prescribe different and individual performance standards, to the extent
appropriate and feasible, for different electronic products so as to recognize their different
operating characteristics and uses.
(3) The performance standards prescribed under this section shall not apply to any electronic
product which is intended solely for export if (A) such product and the outside of any shipping
container used in the export of such product are labeled or tagged to show that such product is
intended for export, and (B) such product meets all the applicable requirements of the country
to which such product is intended for export.
(4) The Secretary may by regulation amend or revoke any performance standard prescribed
under this section.
(5) The Secretary may exempt from the provisions of this section any electronic product
intended for use by departments or agencies of the United States provided such department or
agency has prescribed procurement specifications governing emissions of electronic product
radiation and provided further that such product is of a type used solely or predominantly by
departments or agencies of the United States.
(b) The provisions of subchapter II of chapter 5 of title 5 of the United States Code (relating to
the administrative procedure for rulemaking), and of chapter 7 of such title (relating to judicial
review), shall apply with respect to any regulation prescribing, amending, or revoking any
standard prescribed under this section.
(c) Each regulation prescribing, amending, or revoking a standard shall specify the date on
which it shall take effect which, in the case of any regulation prescribing, or amending any
standard, may not be sooner than one year or not later than two years after the date on which
such regulation is issued, unless the Secretary finds, for good cause shown, that an earlier or
later effective date is in the public interest and publishes in the Federal Register his reason for
such finding, in which case such earlier or later date shall apply.
(d)(1) In a case of actual controversy as to the validity of any regulation issued under this
section prescribing, amending, or revoking a performance standard, any person who will be
adversely affected by such regulation when it is effective may at any time prior to the sixtieth
day after such regulation is issued file a petition with the United States court of appeals for the
circuit wherein such person resides or has his principal place of business, for a judicial review
of such regulation. A copy of the petition shall be forthwith transmitted by the clerk of the court
to the Secretary or other officer designated by him for that purpose. The Secretary thereupon
shall file in the court the record of the proceedings on which the Secretary based the regulation,
as provided in section 2112 of title 28 of the United States Code.
(2) If the petitioner applies to the court for leave to adduce additional evidence, and shows to
the satisfaction of the court that such additional evidence is material and that there were
reasonable grounds for the failure to adduce such evidence in the proceeding before the
Secretary, the court may order such additional evidence (and evidence in rebuttal thereof) to
be taken before the Secretary, and to be adduced upon the hearing, in such manner and upon
such terms and conditions as to the court may seem proper. The Secretary may modify his
findings, or make new findings, by reason of the additional evidence so taken, and he shall file
such modified or new findings, and his recommendations, if any, for the modification or setting
aside of his original regulation, with the return of such additional evidence.
(3) Upon the filing of the petition referred to in paragraph (1) of this subsection, the court shall
have jurisdiction to review the regulation in accordance with chapter 7 of title 5 of the United
States Code and to grant appropriate relief as provided in such chapter.
(4) The judgment of the court affirming or setting aside, in whole or in part, any such regulation
of the Secretary shall be final, subject to review by the Supreme Court of the United States
upon certiorari or certification as provided in section 1254 of title 28 of the United States Code.
(5) Any action instituted under this subsection shall survive, notwithstanding any change in the
person occupying the office of Secretary or any vacancy in such office.
(6) The remedies provided for in this subsection shall be in addition to and not in substitution
for any other remedies provided by law.
(e) A certified copy of the transcript of the record and administrative proceedings under this
section shall be furnished by the Secretary to any interested party at his request, and payment
of the costs thereof, and shall be admissible in any criminal, exclusion of imports, or other
proceeding arising under or in respect of this subchapter, irrespective of whether proceedings
with respect to the regulation have previously been initiated or become final under this section.
(f)(1)(A) The Secretary shall establish a Technical Electronic Product Radiation Safety
Standards Committee (hereafter in this subchapter referred to as the Committee") which he
shall consult before prescribing any standard under this section. The Committee shall be
appointed by the Secretary, after consultation with public and private agencies concerned with
the technical aspect of electronic product radiation safety, and shall be composed of fifteen
members each of whom shall be technically qualified by training and experience in one or
more fields of science or engineering applicable to electronic product radiation safety, as
follows:
(i) Five members shall be selected from governmental agencies, including State and Federal
Governments;
(ii) Five members shall be selected from the affected industries after consultation with industry
representatives; and
(iii) Five members shall be selected from the general public, of which at least one shall be a
representative of organized labor.
(B) The Committee may propose electronic product radiation safety standards to the Secretary
for his consideration. All proceedings of the Committee shall be recorded and the record of
each such proceeding shall be available for public inspection.
(2) Payments to members of the Committee who are not officers or employees of the United
States pursuant to subsection (c) of section 208 of the Public Health Service Act shall not
render members of the Committee officers or employees of the United States for any purpose.
(g) The Secretary shall review and evaluate on a continuing basis testing programs carried out
by industry to assure the adequacy of safeguards against hazardous electronic product
radiation and to assure that electronic products comply with standards prescribed under this
section.
(h) Every manufacturer of an electronic product to which is applicable a standard in effect
under this section shall furnish to the distributor or dealer at the time of delivery of such
product, in the form of a label or tag permanently affixed to such product or in such manner as
approved by the Secretary, the certification that such product conforms to all applicable
standards under this section. Such certification shall be based upon a test, in accordance with
such standard, of the individual article to which it is attached or upon a testing program which
is in accord with good manufacturing practice and which has not been disapproved by the
Secretary (in such manner as he shall prescribe by regulation) on the grounds that it does not
assure the adequacy of safeguards against hazardous electronic product radiation or that it
does not assure that electronic products comply with the standards prescribed under this
section.
NOTIFICATION OF DEFECTS IN, AND REPAIR OR REPLACEMENT OF ELECTRONIC
PRODUCTS
SEC. 535. [21 U.S.C. 360ll] (a)(1) Every manufacturer of electronic products, who discovers
that an electronic product produced, assembled, or imported by him has a defect which relates
to the safety of use of such product by reason of the emission of electronic product radiation,
or that an electronic product produced, assembled, or imported by him on or after the effective
date of an applicable standard prescribed pursuant to section 534 fails to comply with such
standard, shall immediately notify the Secretary of such defect or failure to comply if such
product has left the place of manufacture and shall (except as authorized by paragraph (2))
with reasonable promptness furnish notification of such defect or failure to the persons (where
known to the manufacturer) specified in subsection (b) of this section.
(2) If, in the opinion of such manufacturer, the defect or failure to comply is not such as to
create a significant risk of injury, including genetic injury, to any person, he may, at the time of
giving notice to the Secretary of such defect or failure to comply, apply to the Secretary for an
exemption from the requirement of notice to the persons specified in subsection (b). If such
application states reasonable grounds for such exemption, the Secretary shall afford such
manufacturer an opportunity to present his views and evidence in support of the application,
the burden of proof being on the manufacturer. If, after such presentation, the Secretary is
satisfied that such defect or failure to comply is not such as to create a significant risk of injury,
including genetic injury, to any person, he shall exempt such manufacturer from the
requirement of notice to the persons specified in subsection (b) of this section and from the
requirements of repair or replacement imposed by subsection (f) of this section.
(b) The notification (other than to the Secretary) required by paragraph (1) of subsection (a) of
this section shall be accomplished—
(1) by certified mail to the first purchaser of such product for purposes other than resale, and to
any subsequent transferee of such product; and
(2) by certified mail or other more expeditious means to the dealers or distributors of such
manufacturer to whom such product was delivered.
(c) The notifications required by paragraph (1) of subsection (a) of this section shall contain a
clear description of such defect or failure to comply with an applicable standard, an evaluation
of the hazard reasonably related to such defect or failure to comply, and a statement of the
measures to be taken to repair such defect. In the case of a notification to a person referred to
in subsection (b) of this section, the notification shall also advise the person of his rights under
subsection (f) of this section.
(d) Every manufacturer of electronic products shall furnish to the Secretary a true or
representative copy of all notices, bulletins, and other communications to the dealers or
distributors of such manufacturer or to purchasers (or subsequent transferees) of electronic
products of such manufacturer regarding any such defect in such product or any such failure to
comply with a standard applicable to such product. The Secretary shall disclose to the public
so much of the information contained in such notice or other information obtained under
section 537 as he deems will assist in carrying out the purposes of this subchapter, but he
shall not disclose any information which contains or relates to a trade secret or other matter
referred to in section 1905 of title 18 of the United States Code unless he determines that it is
necessary to carry out the purposes of this subchapter.
(e) If through testing, inspection, investigation, or research carried out pursuant to this
subchapter, or examination of reports submitted pursuant to section 537, or otherwise, the
Secretary determines that any electronic product—
(1) does not comply with an applicable standard prescribed pursuant to section 534; or
(2) contains a defect which relates to the safety of use of such product by reason of the
emission of electronic product radiation;
he shall immediately notify the manufacturer of such product of such defect or failure to comply.
The notice shall contain the findings of the Secretary and shall include all information upon
which the findings are based. The Secretary shall afford such manufacturer an opportunity to
present his views and evidence in support thereof, to establish that there is no failure of
compliance or that the alleged defect does not exist or does not relate to safety of use of the
product by reason of the emission of such radiation hazard. If after such presentation by the
manufacturer the Secretary determines that such product does not comply with an applicable
standard prescribed pursuant to section 534, or that it contains a defect which relates to the
safety of use of such product by reason of the emission of electronic product radiation, the
Secretary shall direct the manufacturer to furnish the notification specified in subsection (c) of
this section to the persons specified in paragraphs (1) and (2) of subsection (b) of this section
(where known to the manufacturer), unless the manufacturer has applied for an exemption
from the requirement of such notification on the ground specified in paragraph (2) of
subsection (a) and the Secretary is satisfied that such noncompliance or defect is not such as
to create a significant risk of injury, including genetic injury, to any person.
(f) If any electronic product is found under subsection (a) or (e) to fail to comply with an
applicable standard prescribed under this subchapter or to have a defect which relates to the
safety of use of such product, and the notification specified in subsection (c) is required to be
furnished on account of such failure or defect, the manufacturer of such product shall (1)
without charge, bring such product into conformity with such standard or remedy such defect
and provide reimbursement for any expenses for transportation of such product incurred in
connection with having such product brought into conformity or having such defect remedied,
(2) replace such product with a like or equivalent product which complies with each applicable
standard prescribed under this subchapter and which has no defect relating to the safety of its
use, or (3) make a refund of the cost of such product. The manufacturer shall take the action
required by this subsection in such manner, and with respect to such persons, as the
Secretary by regulations shall prescribe.
(g) This section shall not apply to any electronic product that was manufactured before the
date of the enactment of this subchapter 1 .
IMPORTS
SEC. 536. [21 U.S.C. 360mm] (a) Any electronic product offered for importation into the United
States which fails to comply with an applicable standard prescribed under this subchapter, or
to which is not affixed a certification in the form of a label or tag in conformity with section
534(h) shall be refused admission into the United States. The Secretary of the Treasury shall
deliver to the Secretary of Health and Human Services, upon the latter’s request, samples of
electronic products which are being imported or offered for import into the United States, giving
notice thereof to the owner or consignee, who may have a hearing before the Secretary of
Health and Human Services. If it appears from an examination of such samples or otherwise
that any electronic product fails to comply with applicable standards prescribed pursuant to
section 534, then, unless subsection (b) of this section applies and is complied with, (1) such
electronic product shall be refused admission, and (2) the Secretary of the Treasury shall
cause the destruction of such electronic product unless such article is exported, under
regulations prescribed by the Secretary of the Treasury, within 90 days after the date of notice
of refusal of admission or within such additional time as may be permitted by such regulations.
(b) If it appears to the Secretary of Health and Human Services that any electronic product
refused admission pursuant to subsection (a) of this section can be brought into compliance
with applicable standards prescribed pursuant to section 534, final determination as to
admission of such electronic product may be deferred upon filing of timely written application
by the owner or consignee and the execution by him of a good and sufficient bond providing
for the payment of such liquidated damages in the event of default as the Secretary of Health
and Human Services may by regulation prescribe. If such application is filed and such bond is
executed the Secretary of Health and Human Services may, in accordance with rules
prescribed by him, permit the applicant to perform such operations with respect to such
electronic product as may be specified in the notice of permission.
(c) All expenses (including travel, per diem or subsistence, and salaries of officers or
employees of the United States) in connection with the destruction provided for in subsection
(a) of this section and the supervision of operations provided for in subsection (b) of this
section, and all expenses in connection with the storage, cartage, or labor with respect to any
electronic product refused admission pursuant to subsection (a) of this section, shall be paid
by the owner or consignee, and, in event of default, shall constitute a lien against any future
importations made by such owner or consignee.
(d) It shall be the duty of every manufacturer offering an electronic product for importation into
the United States to designate in writing an agent upon whom service of all administrative and
judicial processes, notices, orders, decisions, and requirements may be made for and on
behalf of said manufacturer, and to file such designation with the Secretary, which designation
may from time to time be changed by like writing, similarly filed. Service of all administrative
and judicial processes, notices, orders, decisions, and requirements may be made upon said
manufacturer by service upon such designated agent at his office or usual place of residence
with like effect as if made personally upon said manufacturer, and in default of such
designation of such agent, service of process, notice, order, requirement, or decision in any
proceeding before the Secretary or in any judicial proceeding for enforcement of this
subchapter or any standards prescribed pursuant to this subchapter may be made by posting
such process, notice, order, requirement, or decision in the Office of the Secretary or in a place
designated by him by regulation.
INSPECTION AND REPORTS
SEC. 537. [21 U.S.C. 360nn] (a) If the Secretary finds for good cause that the methods, tests,
or programs related to electronic product radiation safety in a particular factory, warehouse, or
establishment in which electronic products are manufactured or held, may not be adequate or
reliable, officers or employees duly designated by the Secretary, upon presenting appropriate
credentials and a written notice to the owner, operator, or agent in charge, are thereafter
authorized (1) to enter, at reasonable times, any area in such factory, warehouse, or
establishment in which the manufacturer’s tests (or testing programs) required by section
534(h) are carried out, and (2) to inspect, at reasonable times and within reasonable limits and
in a reasonable manner, the facilities and procedures within such area which are related to
electronic product radiation safety. Each such inspection shall be commenced and completed
with reasonable promptness. In addition to other grounds upon which good cause may be
found for purposes of this subsection, good cause will be considered to exist in any case
where the manufacturer has introduced into commerce any electronic product which does not
comply with an applicable standard prescribed under this subchapter and with respect to
which no exemption from the notification requirements has been granted by the Secretary
under section 535(a)(2) or 535(e).
(b) Every manufacturer of electronic products shall establish and maintain such records
(including testing records), make such reports, and provide such information, as the Secretary
may reasonably require to enable him to determine whether such manufacturer has acted or is
acting in compliance with this subchapter and standards prescribed pursuant to this
subchapter and shall, upon request of an officer or employee duly designated by the Secretary,
permit such officer or employee to inspect appropriate books, papers, records, and documents
relevant to determining whether such manufacturer has acted or is acting in compliance with
standards prescribed pursuant to this subchapter.
(c) Every manufacturer of electronic products shall provide to the Secretary such performance
data and other technical data related to safety as may be required to carry out the purposes of
this subchapter. The Secretary is authorized to require the manufacturer to give such
notification of such performance and technical data at the time of original purchase to the
ultimate purchaser of the electronic product, as he determines necessary to carry out the
purposes of this subchapter after consulting with the affected industry.
(d) Accident and investigation reports made under this subchapter by any officer, employee, or
agent of the Secretary shall be available for use in any civil, criminal, or other judicial
proceeding arising out of such accident. Any such officer, employee, or agent may be required
to testify in such proceedings as to the fact developed in such investigations. Any such report
shall be made available to the public in a manner which need not identify individuals. All
reports on research projects, demonstration projects, and other related activities shall be
public information.
(e) The Secretary or his representative shall not disclose any information reported to or
otherwise obtained by him, pursuant to subsection (a) or (b) of this section, which concerns
any information which contains or relates to a trade secret or other matter referred to in section
1905 of title 18 of the United States Code, except that such information may be disclosed to
other officers or employees of the Department and of other agencies concerned with carrying
out this subchapter or when relevant in any proceeding under this subchapter. Nothing in this
section shall authorize the withholding of information by the Secretary, or by any officers or
employees under his control, from the duly authorized committees of the Congress.
(f) The Secretary may by regulation (1) require dealers and distributors of electronic products,
to which there are applicable standards prescribed under this subchapter and the retail prices
of which is not less than $50, to furnish manufacturers of such products such information as
may be necessary to identify and locate, for purposes of section 535, the first purchasers of
such products for purposes other than resale, and (2) require manufacturers to preserve such
information. Any regulation establishing a requirement pursuant to clause (1) of the preceding
sentence shall (A) authorize such dealers and distributors to elect, in lieu of immediately
furnishing such information to the manufacturer, to hold and preserve such information until
advised by the manufacturer or Secretary that such information is needed by the manufacturer
for purposes of section 535, and (B) provide that the dealer or distributor shall, upon making
such election, give prompt notice of such election (together with information identifying the
notifier and the product) to the manufacturer and shall, when advised by the manufacturer or
Secretary, of the need therefor for the purposes of section 535, immediately furnish the
manufacturer with the required information. If a dealer or distributor discontinues the dealing in
or distribution of electronic products, he shall turn the information over to the manufacturer.
Any manufacturer receiving information pursuant to this subsection concerning first
purchasers of products for purposes other than resale shall treat it as confidential and may use
it only if necessary for the purpose of notifying persons pursuant to section 535(a).
PROHIBITED ACTS
SEC. 538. [21 U.S.C. 360oo] (a) It shall be unlawful—
(1) for any manufacturer to introduce, or to deliver for introduction, into commerce, or to import
into the United States, any electronic product which does not comply with an applicable
standard prescribed pursuant to section 534;
(2) for any person to fail to furnish any notification or other material or information required by
section 535 or 537; or to fail to comply with the requirements of section 535(f);
(3) for any person to fail or to refuse to establish or maintain records required by this
subchapter or to permit access by the Secretary or any of his duly authorized representatives
to, or the copying of, such records, or to permit entry or inspection, as required by or pursuant
to section 537;
(4) for any person to fail or to refuse to make any report required pursuant to section 537(b) or
to furnish or preserve any information required pursuant to section 537(f); or
(5) for any person (A) to fail to issue a certification as required by section 534(h), or (B) to
issue such a certification when such certification is not based upon a test or testing program
meeting the requirements of section 534(h) or when the issuer, in the exercise of due care,
would have reason to know that such certification is false or misleading in a material respect.
(b) The Secretary may exempt any electronic product, or class thereof, from all or part of
subsection (a), upon such conditions as he may find necessary to protect the public health or
welfare, for the purpose of research, investigations, studies, demonstrations, or training, or for
reasons of national security.
ENFORCEMENT
SEC. 539. [21 U.S.C. 360pp] (a) The district courts of the United States shall have jurisdiction,
for cause shown, to restrain violations of section 538 and to restrain dealers and distributors of
electronic products from selling or otherwise disposing of electronic products which do not
conform to an applicable standard prescribed pursuant to section 534 except when such
products are disposed of by returning them to the distributor or manufacturer from whom they
were obtained. The district courts of the United States shall also have jurisdiction in
accordance with section 1355 of title 28 of the United States Code to enforce the provisions of
subsection (b) of this section.
(b)(1) Any person who violates section 538 shall be subject to a civil penalty of not more than
$1,000. For purposes of this subsection, any such violation shall with respect to each
electronic product involved, or with respect to each act or omission made unlawful by section
538, constitute a separate violation, except that the maximum civil penalty imposed on any
person under this subsection for any related series of violations shall not exceed $300,000.
(2) Any such civil penalty may on application be remitted or mitigated by the Secretary. In
determining the amount of such penalty, or whether it should be remitted or mitigated and in
what amount, the appropriateness of such penalty to the size of the business of the person
charged and the gravity of the violation shall be considered. The amount of such penalty, when
finally determined, may be deducted from any sums owing by the United States to the person
charged.
(c) Actions under subsections (a) and (b) of this section may be brought in the district court of
the United States for the district wherein any act or omission or transaction constituting the
violation occurred, or in such court for the district where the defendant is found or transacts
business, and process in such cases may be served in any other district of which the
defendant is an inhabitant or wherever the defendant may be found.
(d) Nothing in this subchapter shall be construed as requiring the Secretary to report for the
institution of proceedings minor violations of this subchapter whenever he believes that the
public interest will be adequately served by a suitable written notice or warning.
(e) Except as provided in the first sentence of section 542, compliance with this subchapter or
any regulations issued thereunder shall not relieve any person from liability at common law or
under statutory law.
(f) The remedies provided for in this subchapter shall be in addition to and not in substitution
for any other remedies provided by law.
[Sec. 540 repealed by P.L. 105–362, § 601(a)(2)(A).]
FEDERAL-STATE COOPERATION
SEC. 541. 2 [21 U.S.C. 360rr] The Secretary is authorized (1) to accept from State and local
authorities engaged in activities related to health or safety or consumer protection, on a
reimbursable basis or otherwise, any assistance in the administration and enforcement of this
subchapter which he may request and which they may be able and willing to provide and, if so
agreed, may pay in advance or otherwise for the reasonable cost of such assistance, and (2)
he may, for the purpose of conducting examinations, investigations, and inspections,
commission any officer or employee of any such authority as an officer of the Department.
EFFECT ON STATE STANDARDS
SEC. 542. [21 U.S.C. 360ss] Whenever any standard prescribed pursuant to section 534 with
respect to an aspect of performance of an electronic product is in effect, no State or political
subdivision of a State shall have any authority either to establish, or to continue in effect, any
standard which is applicable to the same aspect of performance of such product and which is
not identical to the Federal standard. Nothing in this subchapter shall be construed to prevent
the Federal Government or the government of any State or political subdivision thereof from
establishing a requirement with respect to emission of radiation from electronic products
procured for its own use if such requirement imposes a more restrictive standard than that
required to comply with the otherwise applicable Federal standard.
Footnotes: Chapter V, Subchapter C
1. This subchapter was enacted by Public Law 90–602, which was enacted October 18, 1968.
(The subchapter was originally enacted as part of the Public Health Service Act, and was
transferred to this Act by section 19 of Public Law 101–629.)
2. Section 540 was repealed by section 601(a)(2)(A) of Public Law 105–362 (112 Stat. 3285).
CHAPTER V--DRUGS AND DEVICES
SUBCHAPTER D —DISSEMINATION OF TREATMENT INFORMATION 1
SEC. 551. [21 U.S.C. 360aaa] REQUIREMENTS FOR DISSEMINATION OF TREATMENT
INFORMATION ON DRUGS OR DEVICES.
(a) IN GENERAL.—Notwithstanding sections 301(d), 502(f), and 505, and section 351 of the
Public Health Service Act (42 U.S.C. 262), a manufacturer may disseminate to—
(1) a health care practitioner;
(2) a pharmacy benefit manager;
(3) a health insurance issuer;
(4) a group health plan; or
(5) a Federal or State governmental agency;
written information concerning the safety, effectiveness, or benefit of a use not described in the
approved labeling of a drug or device if the manufacturer meets the requirements of
subsection (b).
(b) SPECIFIC REQUIREMENTS.—A manufacturer may disseminate information under
subsection (a) on a new use only if—
(1)(A) in the case of a drug, there is in effect for the drug an application filed under subsection
(b) or (j) of section 505 or a biologics license issued under section 351 of the Public Health
Service Act; or
(B) in the case of a device, the device is being commercially distributed in accordance with a
regulation under subsection (d) or (e) of section 513, an order under subsection (f) of such
section, or the approval of an application under section 515;
(2) the information meets the requirements of section 552;
(3) the information to be disseminated is not derived from clinical research conducted by
another manufacturer or if it was derived from research conducted by another manufacturer,
the manufacturer disseminating the information has the permission of such other manufacturer
to make the dissemination;
(4) the manufacturer has, 60 days before such dissemination, submitted to the Secretary—
(A) a copy of the information to be disseminated; and
(B) any clinical trial information the manufacturer has
relating to the safety or effectiveness of the new use, any reports of clinical experience
pertinent to the safety of the new use, and a summary of such information;
(5) the manufacturer has complied with the requirements of section 554 (relating to a
supplemental application for such use);
(6) the manufacturer includes along with the information to be disseminated under this
subsection—
(A) a prominently displayed statement that discloses—
(i) that the information concerns a use of a drug or device that has not been approved or
cleared by the Food and Drug Administration;
(ii) if applicable, that the information is being disseminated at the expense of the manufacturer;
(iii) if applicable, the name of any authors of the information who are employees of, consultants
to, or have received compensation from, the manufacturer, or who have a significant financial
interest in the manufacturer;
(iv) the official labeling for the drug or device and all updates with respect to the labeling;
(v) if applicable, a statement that there are products or treatments that have been approved or
cleared for the use that is the subject of the information being disseminated pursuant to
subsection (a)(1); and
(vi) the identification of any person that has provided funding for the conduct of a study relating
to the new use of a drug or device for which such information is being disseminated; and
(B) a bibliography of other articles from a scientific reference publication or scientific or medical
journal that have been previously published about the use of the drug or device covered by the
information disseminated (unless the information already includes such bibliography).
(c) ADDITIONAL INFORMATION.—If the Secretary determines, after providing notice of such
determination and an opportunity for a meeting with respect to such determination, that the
information submitted by a manufacturer under subsection (b)(3)(B), with respect to the use of
a drug or device for which the manufacturer intends to disseminate information, fails to provide
data, analyses, or other written matter that is objective and balanced, the Secretary may
require the manufacturer to disseminate—
(1) additional objective and scientifically sound information that pertains to the safety or
effectiveness of the use and is necessary to provide objectivity and balance, including any
information that the manufacturer has submitted to the Secretary or, where appropriate, a
summary of such information or any other information that the Secretary has authority to make
available to the public; and
(2) an objective statement of the Secretary, based on data or other scientifically sound
information available to the Secretary, that bears on the safety or effectiveness of the new use
of the drug or device.
SEC. 552. [21 U.S.C. 360aaa–1] INFORMATION AUTHORIZED TO BE DISSEMINATED.
(a) AUTHORIZED INFORMATION.—A manufacturer may disseminate information under
section 551 on a new use only if the information—
(1) is in the form of an unabridged—
(A) reprint or copy of an article, peer-reviewed by experts qualified by scientific training or
experience to evaluate the safety or effectiveness of the drug or device involved, which was
published in a scientific or medical journal (as defined in section 556(5)), which is about a
clinical investigation with respect to the drug or device, and which would be considered to be
scientifically sound by such experts; or
(B) reference publication, described in subsection (b), that includes information about a clinical
investigation with respect to the drug or device that would be considered to be scientifically
sound by experts qualified by scientific training or experience to evaluate the safety or
effectiveness of the drug or device that is the subject of such a clinical investigation; and
(2) is not false or misleading and would not pose a significant risk to the public health.
(b) REFERENCE PUBLICATION.—A reference publication referred to in subsection (a)(1)(B)
is a publication that—
(1) has not been written, edited, excerpted, or published specifically for, or at the request of, a
manufacturer of a drug or device;
(2) has not been edited or significantly influenced by such a manufacturer;
(3) is not solely distributed through such a manufacturer but is generally available in
bookstores or other distribution channels where medical textbooks are sold;
(4) does not focus on any particular drug or device of a manufacturer that disseminates
information under section 551and does not have a primary focus on new uses of drugs or
devices that are marketed or under investigation by a manufacturer supporting the
dissemination of information; and
(5) presents materials that are not false or misleading.
SEC. 553. [21 U.S.C. 360aaa–2] ESTABLISHMENT OF LIST OF ARTICLES AND
PUBLICATIONS DISSEMINATED AND LIST OF PROVIDERS THAT RECEIVED ARTICLES
AND REFERENCE PUBLICATIONS.
(a) IN GENERAL.—A manufacturer may disseminate information under section 551 on a new
use only if the manufacturer prepares and submits to the Secretary biannually—
(1) a list containing the titles of the articles and reference publications relating to the new use
of drugs or devices that were disseminated by the manufacturer to a person described in
section 551(a) for the 6-month period preceding the date on which the manufacturer submits
the list to the Secretary; and
(2) a list that identifies the categories of providers (as described in section 551(a)) that
received the articles and reference publications for the 6-month period described in paragraph
(1).
(b) RECORDS.—A manufacturer that disseminates information under section 551 shall keep
records that may be used by the manufacturer when, pursuant to section 555, such
manufacturer is required to take corrective action and shall be made available to the Secretary,
upon request, for purposes of ensuring or taking corrective action pursuant to such section.
Such records, at the Secretary’s discretion, may identify the recipient of information provided
pursuant to section 551 or the categories of such recipients.
SEC. 554. [21 U.S.C. 360aaa–3] REQUIREMENT REGARDING SUBMISSION OF
SUPPLEMENTAL APPLICATION FOR NEW USE; EXEMPTION FROM REQUIREMENT.
(a) IN GENERAL.—A manufacturer may disseminate information under section 551 on a new
use only if—
(1)(A) the manufacturer has submitted to the Secretary a supplemental application for such
use; or
(B) the manufacturer meets the condition described in subsection (b) or (c) (relating to a
certification that the manufacturer will submit such an application); or
(2) there is in effect for the manufacturer an exemption under subsection (d) from the
requirement of paragraph (1).
(b) CERTIFICATION ON SUPPLEMENTAL APPLICATION; CONDITION IN CASE OF
COMPLETED STUDIES.—For purposes of subsection (a)(1)(B), a manufacturer may
disseminate information on a new use if the manufacturer has submitted to the Secretary an
application containing a certification that—
(1) the studies needed for the submission of a supplemental application for the new use have
been completed; and
(2) the supplemental application will be submitted to the Secretary not later than 6 months
after the date of the initial dissemination of information under section 551.
(c) CERTIFICATION ON SUPPLEMENTAL APPLICATION; CONDITION IN CASE OF
PLANNED STUDIES.—
(1) IN GENERAL.—For purposes of subsection (a)(1)(B), a manufacturer may disseminate
information on a new use if—
(A) the manufacturer has submitted to the Secretary an application containing—
(i) a proposed protocol and schedule for conducting the studies needed for the submission of a
supplemental application for the new use; and
(ii) a certification that the supplemental application will be submitted to the Secretary not later
than 36 months after the date of the initial dissemination of information under section 551 (or,
as applicable, not later than such date as the Secretary may specify pursuant to an extension
under paragraph (3)); and
(B) the Secretary has determined that the proposed protocol is adequate and that the schedule
for completing such studies is reasonable.
(2) PROGRESS REPORTS ON STUDIES.—A manufacturer that submits to the Secretary an
application under paragraph (1) shall submit to the Secretary periodic reports describing the
status of the studies involved.
(3) EXTENSION OF TIME REGARDING PLANNED STUDIES.—The period of 36 months
authorized in paragraph (1)(A)(ii) for the completion of studies may be extended by the
Secretary if—
(A) the Secretary determines that the studies needed to submit such an application cannot be
completed and submitted within 36 months; or
(B) the manufacturer involved submits to the Secretary a written request for the extension and
the Secretary determines that the manufacturer has acted with due diligence to conduct the
studies in a timely manner, except that an extension under this subparagraph may not be
provided for more than 24 additional months.
(d) EXEMPTION FROM REQUIREMENT OF SUPPLEMENTAL APPLICATION.—
(1) IN GENERAL.—For purposes of subsection (a)(2), a manufacturer may disseminate
information on a new use if—
(A) the manufacturer has submitted to the Secretary an application for an exemption from
meeting the requirement of subsection (a)(1); and
(B)(i) the Secretary has approved the application in accordance with paragraph (2); or
(ii) the application is deemed under paragraph (3)(A) to have been approved (unless such
approval is terminated pursuant to paragraph (3)(B)).
(2) CONDITIONS FOR APPROVAL.—The Secretary may approve an application under
paragraph (1) for an exemption if the Secretary makes a determination described in
subparagraph (A) or (B), as follows:
(A) The Secretary makes a determination that, for reasons defined by the Secretary, it would
be economically prohibitive with respect to such drug or device for the manufacturer to incur
the costs necessary for the submission of a supplemental application. In making such
determination, the Secretary shall consider (in addition to any other considerations the
Secretary finds appropriate)—
(i) the lack of the availability under law of any period during which the manufacturer would
have exclusive marketing rights with respect to the new use involved; and
(ii) the size of the population expected to benefit from approval of the supplemental
application.
(B) The Secretary makes a determination that, for reasons defined by the Secretary, it would
be unethical to conduct the studies necessary for the supplemental application. In making
such determination, the Secretary shall consider (in addition to any other considerations the
Secretary finds appropriate) whether the new use involved is the standard of medical care for
a health condition.
(3) TIME FOR CONSIDERATION OF APPLICATION; DEEMED APPROVAL.—
(A) IN GENERAL.—The Secretary shall approve or deny an application under paragraph (1)
for an exemption not later than 60 days after the receipt of the application. If the Secretary
does not comply with the preceding sentence, the application is deemed to be approved.
(B) TERMINATION OF DEEMED APPROVAL.—If pursuant to a deemed approval under
subparagraph (A) a manufacturer disseminates written information under section 551 on a
new use, the Secretary may at any time terminate such approval and under section 555(b)(3)
order the manufacturer to cease disseminating the information.
(e) REQUIREMENTS REGARDING APPLICATIONS.—Applications under this section shall
be submitted in the form and manner prescribed by the Secretary.
SEC. 555. [21 U.S.C. 360aaa–4] CORRECTIVE ACTIONS; CESSATION OF
DISSEMINATION.
(a) POSTDISSEMINATION DATA REGARDING SAFETY AND EFFECTIVENESS.—
(1) CORRECTIVE ACTIONS.—With respect to data received by the Secretary after the
dissemination of information under section 551 by a manufacturer has begun (whether
received pursuant to paragraph (2) or otherwise), if the Secretary determines that the data
indicate that the new use involved may not be effective or may present a significant risk to
public health, the Secretary shall, after consultation with the manufacturer, take such action
regarding the dissemination of the information as the Secretary determines to be appropriate
for the protection of the public health, which may include ordering that the manufacturer cease
the dissemination of the information.
(2) RESPONSIBILITIES OF MANUFACTURERS TO SUBMIT DATA.—After a manufacturer
disseminates information under section 551, the manufacturer shall submit to the Secretary a
notification of any additional knowledge of the manufacturer on clinical research or other data
that relate to the safety or effectiveness of the new use involved. If the manufacturer is in
possession of the data, the notification shall include the data. The Secretary shall by regulation
establish the scope of the responsibilities of manufacturers under this paragraph, including
such limits on the responsibilities as the Secretary determines to be appropriate.
(b) CESSATION OF DISSEMINATION.—
(1) FAILURE OF MANUFACTURER TO COMPLY WITH REQUIREMENTS.— The Secretary
may order a manufacturer to cease the dissemination of information pursuant to section 551 if
the Secretary determines that the information being disseminated does not comply with the
requirements established in this subchapter. Such an order may be issued only after the
Secretary has provided notice to the manufacturer of the intent of the Secretary to issue the
order and (unless paragraph (2)(B) applies) has provided an opportunity for a meeting with
respect to such intent. If the failure of the manufacturer constitutes a minor violation of this
subchapter, the Secretary shall delay issuing the order and provide to the manufacturer an
opportunity to correct the violation.
(2) SUPPLEMENTAL APPLICATIONS.—The Secretary may order a manufacturer to cease
the dissemination of information pursuant to section 551 if—
(A) in the case of a manufacturer that has submitted a supplemental application for a new use
pursuant to section 554(a)(1), the Secretary determines that the supplemental application
does not contain adequate information for approval of the new use for which the application
was submitted;
(B) in the case of a manufacturer that has submitted a certification under section 554(b), the
manufacturer has not, within the 6-month period involved, submitted the supplemental
application referred to in the certification; or
(C) in the case of a manufacturer that has submitted a certification under section 554(c) but
has not yet submitted the supplemental application referred to in the certification, the
Secretary determines, after an informal hearing, that the manufacturer is not acting with due
diligence to complete the studies involved.
(3) TERMINATION OF DEEMED APPROVAL OF EXEMPTION REGARDING
SUPPLEMENTAL APPLICATIONS.—If under section 554(d)(3) the Secretary terminates a
deemed approval of an exemption, the Secretary may order the manufacturer involved to
cease disseminating the information. A manufacturer shall comply with an order under the
preceding sentence not later than 60 days after the receipt of the order.
(c) CORRECTIVE ACTIONS BY MANUFACTURERS.—
(1) IN GENERAL.—In any case in which under this section the Secretary orders a
manufacturer to cease disseminating information, the Secretary may order the manufacturer to
take action to correct the information that has been disseminated, except as provided in
paragraph (2).
(2) TERMINATION OF DEEMED APPROVAL OF EXEMPTION REGARDING
SUPPLEMENTAL APPLICATIONS.—In the case of an order under subsection (b)(3) to cease
disseminating information, the Secretary may not order the manufacturer involved to take
action to correct the information that has been disseminated unless the Secretary determines
that the new use described in the information would pose a significant risk to the public health.
SEC. 556. [21 U.S.C. 360aaa–5] DEFINITIONS.
For purposes of this subchapter:
(1) The term "health care practitioner" means a physician, or other individual who is a provider
of health care, who is licensed under the law of a State to prescribe drugs or devices.
(2) The terms "health insurance issuer" and "group health plan" have the meaning given such
terms under section 2791 of the Public Health Service Act.
(3) The term "manufacturer" means a person who manufactures a drug or device, or who is
licensed by such person to distribute or market the drug or device.
(4) The term "new use"—
(A) with respect to a drug, means a use that is not included in the labeling of the approved drug;
and
(B) with respect to a device, means a use that is not included in the labeling for the approved
or cleared device.
(5) The term "scientific or medical journal" means a scientific or medical publication—
(A) that is published by an organization—
(i) that has an editorial board;
(ii) that utilizes experts, who have demonstrated expertise in the subject of an article under
review by the organization and who are independent of the organization, to review and
objectively select, reject, or provide comments about proposed articles; and
(iii) that has a publicly stated policy, to which the organization adheres, of full disclosure of any
conflict of interest or biases for all authors or contributors involved with the journal or
organization;
(B) whose articles are peer-reviewed and published in accordance with the regular
peer-review procedures of the organization;
(C) that is generally recognized to be of national scope and reputation;
(D) that is indexed in the Index Medicus of the National Library of Medicine of the National
Institutes of Health; and
(E) that is not in the form of a special supplement that has been funded in whole or in part by
one or more manufacturers.
SEC. 557. [21 U.S.C. 360aaa–6] RULES OF CONSTRUCTION.
(a) UNSOLICITED REQUEST.—Nothing in section 551 shall be construed as prohibiting a
manufacturer from disseminating information in response to an unsolicited request from a
health care practitioner.
(b) DISSEMINATION OF INFORMATION ON DRUGS OR DEVICES NOT EVIDENCE OF
INTENDED USE.—Notwithstanding subsection (a), (f), or (o) of section 502, or any other
provision of law, the dissemination of information relating to a new use of a drug or device, in
accordance with section 551, shall not be construed by the Secretary as evidence of a new
intended use of the drug or device that is different from the intended use of the drug or device
set forth in the official labeling of the drug or device. Such dissemination shall not be
considered by the Secretary as labeling, adulteration, or misbranding of the drug or device.
(c) PATENT PROTECTION.—Nothing in section 551 shall affect patent rights in any manner.
(d) AUTHORIZATION FOR DISSEMINATION OF ARTICLES AND FEES FOR REPRINTS OF
ARTICLES.—Nothing in section 551 shall be construed as prohibiting an entity that publishes
a scientific journal (as defined in section 556(5)) from requiring authorization from the entity to
disseminate an article published by such entity or charging fees for the purchase of reprints of
published articles from such entity.
Footnotes: Chapter V, Subchapter D
1. This subchapter was added by section 401(a) of P.L. 105–115. Subsections (d) and (e) of
such section provides the following:
(d) EFFECTIVE DATE.—The amendments made by this section shall take effect 1 year after
the date of enactment of this Act, or upon the Secretary’s issuance of final regulations
pursuant to subsection (c), whichever is sooner.
(e) SUNSET.—The amendments made by this section cease to be effective September 30,
2006, or 7 years after the date on which the Secretary promulgates the regulations described
in subsection (c), whichever is later.
CHAPTER V--DRUGS AND DEVICES
SUBCHAPTER E--GENERAL PROVISIONS RELATING TO DRUGS AND DEVICES
SEC. 561. [21 U.S.C. 360bbb] EXPANDED ACCESS TO UNAPPROVED THERAPIES AND
DIAGNOSTICS.
(a) EMERGENCY SITUATIONS. The Secretary may, under appropriate conditions determined
by the Secretary, authorize the shipment of investigational drugs or investigational devices for
the diagnosis, monitoring, or treatment of a serious disease or condition in emergency
situations.
(b) INDIVIDUAL PATIENT ACCESS TO INVESTIGATIONAL PRODUCTS INTENDED FOR
SERIOUS DISEASES. Any person, acting through a physician licensed in accordance with
State law, may request from a manufacturer or distributor, and any manufacturer or distributor
may, after complying with the provisions of this subsection, provide to such physician an
investigational drug or investigational device for the diagnosis, monitoring, or treatment of a
serious disease or condition if
(1) the licensed physician determines that the person has no comparable or satisfactory
alternative therapy available to diagnose, monitor, or treat the disease or condition involved,
and that the probable risk to the person from the investigational drug or investigational device
is not greater than the probable risk from the disease or condition;
(2) the Secretary determines that there is sufficient evidence of safety and effectiveness to
support the use of the investigational drug or investigational device in the case described in
paragraph (1);
(3) the Secretary determines that provision of the investigational drug or investigational device
will not interfere with the initiation, conduct, or completion of clinical investigations to support
marketing approval; and
(4) the sponsor, or clinical investigator, of the investigational drug or investigational device
submits to the Secretary a clinical protocol consistent with the provisions of section 505(i) or
520(g), including any regulations promulgated under section 505(i) or 520(g), describing the
use of the investigational drug or investigational device in a single patient or a small group of
patients.
(c) TREATMENT INVESTIGATIONAL NEW DRUG APPLICATIONS AND TREATMENT
INVESTIGATIONAL DEVICE EXEMPTIONS. Upon submission by a sponsor or a physician of
a protocol intended to provide widespread access to an investigational drug or investigational
device for eligible patients (referred to in this subsection as an "expanded access protocol"),
the Secretary shall permit such investigational drug or investigational device to be made
available for expanded access under a treatment investigational new drug application or
treatment investigational device exemption if the Secretary determines that
(1) under the treatment investigational new drug application or treatment investigational device
exemption, the investigational drug or investigational device is intended for use in the
diagnosis, monitoring, or treatment of a serious or immediately life-threatening disease or
condition;
(2) there is no comparable or satisfactory alternative therapy available to diagnose, monitor, or
treat that stage of disease or condition in the population of patients to which the investigational
drug or investigational device is intended to be administered;
(3)(A) the investigational drug or investigational device is under investigation in a controlled
clinical trial for the use described in paragraph (1) under an investigational drug application in
effect under section 505(i) or investigational device exemption in effect under section 520(g);
or
(B) all clinical trials necessary for approval of that use of the investigational drug or
investigational device have been completed;
(4) the sponsor of the controlled clinical trials is actively pursuing marketing approval of the
investigational drug or investigational device for the use described in paragraph (1) with due
diligence;
(5) in the case of an investigational drug or investigational device described in paragraph
(3)(A), the provision of the investigational drug or investigational device will not interfere with
the enrollment of patients in ongoing clinical investigations under section 505(i) or 520(g);
(6) in the case of serious diseases, there is sufficient evidence of safety and effectiveness to
support the use described in paragraph (1); and
(7) in the case of immediately life-threatening diseases, the available scientific evidence, taken
as a whole, provides a reasonable basis to conclude that the investigational drug or
investigational device may be effective for its intended use and would not expose patients to
an unreasonable and significant risk of illness or injury.
A protocol submitted under this subsection shall be subject to the provisions of section 505(i)
or 520(g), including regulations promulgated under section 505(i) or 520(g). The Secretary
may inform national, State, and local medical associations and societies, voluntary health
associations, and other appropriate persons about the availability of an investigational drug or
investigational device under expanded access protocols submitted under this subsection. The
information provided by the Secretary, in accordance with the preceding sentence, shall be the
same type of information that is required by section 402(j)(3) of the Public Health Service Act.
(d) TERMINATION. The Secretary may, at any time, with respect to a sponsor, physician,
manufacturer, or distributor described in this section, terminate expanded access provided
under this section for an investigational drug or investigational device if the requirements
under this section are no longer met.
(e) DEFINITIONS. In this section, the terms "investigational drug", "investigational device",
"treatment investigational new drug application", and "treatment investigational device
exemption" shall have the meanings given the terms in regulations prescribed by the
Secretary.
SEC. 562. [21 U.S.C. 360bbb–1] DISPUTE RESOLUTION.
If, regarding an obligation concerning drugs or devices under this Act or section 351 of the
Public Health Service Act, there is a scientific controversy between the Secretary and a person
who is a sponsor, applicant, or manufacturer and no specific provision of the Act involved,
including a regulation promulgated under such Act, provides a right of review of the matter in
controversy, the Secretary shall, by regulation, establish a procedure under which such
sponsor, applicant, or manufacturer may request a review of such controversy, including a
review by an appropriate scientific advisory panel described in section 505(n) or an advisory
committee described in section 515(g)(2)(B). Any such review shall take place in a timely
manner. The Secretary shall promulgate such regulations within 1 year after the date of the
enactment of the Food and Drug Administration Modernization Act of 1997.
SEC. 563. [21 U.S.C. 360bbb–2] CLASSIFICATION OF PRODUCTS.
(a) REQUEST. A person who submits an application or submission (including a petition,
notification, and any other similar form of request) under this Act for a product, may submit a
request to the Secretary respecting the classification of the product as a drug, biological
product, device, or a combination product subject to section 503(g) or respecting the
component of the Food and Drug Administration that will regulate the product. In submitting
the request, the person shall recommend a classification for the product, or a component to
regulate the product, as appropriate.
(b) STATEMENT. Not later than 60 days after the receipt of the request described in
subsection (a), the Secretary shall determine the classification of the product under subsection
(a), or the component of the Food and Drug Administration that will regulate the product, and
shall provide to the person a written statement that identifies such classification or such
component, and the reasons for such determination. The Secretary may not modify such
statement except with the written consent of the person, or for public health reasons based on
scientific evidence.
(c) INACTION OF SECRETARY. If the Secretary does not provide the statement within the
60-day period described in subsection (b), the recommendation made by the person under
subsection (a) shall be considered to be a final determination by the Secretary of such
classification of the product, or the component of the Food and Drug Administration that will
regulate the product, as applicable, and may not be modified by the Secretary except with the
written consent of the person, or for public health reasons based on scientific evidence.
SEC. 564. [21 USC 360bbb-3]- AUTHORIZATION FOR MEDICAL PRODUCTS FOR USE IN
EMERGENCIES.
(a) In General. (1) Emergency uses. Notwithstanding sections 505, 510(k), and 515 of this Act
and section 351 of the Public Health Service Act, and subject to the provisions of this section,
the Secretary may authorize the introduction into interstate commerce, during the effective
period of a declaration under subsection (b), of a drug, device, or biological product intended
for use in an actual or potential emergency (referred to in this section as an "emergency use").
(2) Approval status of product. An authorization under paragraph (1) may authorize an
emergency use of a product that
(A) is not approved, licensed, or cleared for commercial distribution under a provision of law
referred to in such paragraph (referred to in this section as an "unapproved product"); or
(B) is approved, licensed, or cleared under such a provision, but which use is not under such
provision an approved, licensed, or cleared use of the product (referred to in this section as an
"unapproved use of an approved product").
(3) Relation to other uses. An emergency use authorized under paragraph (1) for a product is
in addition to any other use that is authorized for the product under a provision of law referred
to in such paragraph.
(4) Definitions. For purposes of this section:
(A) The term "biological product" has the meaning given such term in section 351 of the Public
Health Service Act.
(B) The term "emergency use" has the meaning indicated for such term in paragraph (1).
(C) The term "product" means a drug, device, or biological product.
(D) The term "unapproved product" has the meaning indicated for such term in paragraph
(2)(A).
(E) The term "unapproved use of an approved product" has the meaning indicated for such
term in paragraph (2)(B).
(b) DECLARATION OF EMERGENCY.
(1) IN GENERAL. The Secretary may declare an emergency justifying the authorization under
this subsection for a product on the basis of
(A) a determination by the Secretary of Homeland Security that there is a domestic emergency,
or a significant potential for a domestic emergency, involving a heightened risk of attack with a
specified biological, chemical, radiological, or nuclear agent or agents;
(B) a determination by the Secretary of Defense that there is a military emergency, or a
significant potential for a military emergency, involving a heightened risk to United States
military forces of attack with a specified biological, chemical, radiological, or nuclear agent or
agents; or
(C) a determination by the Secretary of a public health emergency under section 319 of the
Public Health Service Act that affects, or has a significant potential to affect, national security,
and that involves a specified biological, chemical, radiological, or nuclear agent or agents, or a
specified disease or condition that may be attributable to such agent or agents.
(2) Termination of declaration.
(A) In general. A declaration under this subsection shall terminate upon the earlier of
(i) a determination by the Secretary, in consultation with the Secretary of Defense, that the
circumstances described in paragraph (1) have ceased to exist; or
(ii) the expiration of the one-year period beginning on the date on which the declaration is
made.
(B) Renewal. Notwithstanding subparagraph (A), the Secretary may renew a declaration under
this subsection, and this paragraph shall apply to any such renewal.
(C) Disposition of product. If an authorization under this section with respect to an unapproved
product ceases to be effective as a result of a termination under subparagraph (A) of this
paragraph, the Secretary shall consult with the manufacturer of such product with respect to
the appropriate disposition of the product.
(3) Advance notice of termination. The Secretary shall provide advance notice that a
declaration under this subsection will be terminated. The period of advance notice shall be a
period reasonably determined to provide
(A) in the case of an unapproved product, a sufficient period for disposition of the product,
including the return of such product (except such quantities of product as are necessary to
provide for continued use consistent with subsection (f)(2)) to the manufacturer (in the case of
a manufacturer that chooses to have such product returned); and
(B) in the case of an unapproved use of an approved product, a sufficient period for the
disposition of any labeling, or any information under subsection (e)(2)(B)(ii), as the case may
be, that was provided with respect to the emergency use involved.
(4) Publication. The Secretary shall promptly publish in the Federal Register each declaration,
determination, advance notice of termination, and renewal under this subsection.
(c) Criteria for Issuance of Authorization. The Secretary may issue an authorization under this
section with respect to the emergency use of a product only if, after consultation with the
Director of the National Institutes of Health and the Director of the Centers for Disease Control
and Prevention (to the extent feasible and appropriate given the circumstances of the
emergency involved), the Secretary concludes
(1) that an agent specified in a declaration under subsection (b) can cause a serious or
life-threatening disease or condition;
(2) that, based on the totality of scientific evidence available to the Secretary, including data
from adequate and well-controlled clinical trials, if available, it is reasonable to believe that
(A) the product may be effective in diagnosing, treating, or preventing
(i) such disease or condition; or
(ii) a serious or life-threatening disease or condition caused by a product authorized under this
section, approved or cleared under this Act, or licensed under section 351 of the Public Health
Service Act, for diagnosing, treating, or preventing such a disease or condition caused by such
an agent; and
(B) the known and potential benefits of the product, when used to diagnose, prevent, or treat
such disease or condition, outweigh the known and potential risks of the product;
(3) that there is no adequate, approved, and available alternative to the product for diagnosing,
preventing, or treating such disease or condition; and
(4) that such other criteria as the Secretary may by regulation prescribe are satisfied.
(d) Scope of Authorization. An authorization of a product under this section shall state (1) each
disease or condition that the product may be used to diagnose, prevent, or treat within the
scope of the authorization;
(2) the Secretary's conclusions, made under subsection (c)(2)(B), that the known and potential
benefits of the product, when used to diagnose, prevent, or treat such disease or condition,
outweigh the known and potential risks of the product; and
(3) the Secretary's conclusions, made under subsection (c), concerning the safety and
potential effectiveness of the product in diagnosing, preventing, or treating such diseases or
conditions, including an assessment of the available scientific evidence.
(e) Conditions of Authorization.
(1) Unapproved product.
(A) Required conditions. With respect to the emergency use of an unapproved product, the
Secretary, to the extent practicable given the circumstances of the emergency, shall, for a
person who carries out any activity for which the authorization is issued, establish such
conditions on an authorization under this section as the Secretary finds necessary or
appropriate to protect the public health, including the following:
(i) Appropriate conditions designed to ensure that health care professionals administering the
product are informed
(I) that the Secretary has authorized the emergency use of the product;
(II) of the significant known and potential benefits and risks of the emergency use of the
product, and of the extent to which such benefits and risks are unknown; and
(III) of the alternatives to the product that are available, and of their benefits and risks.
(ii) Appropriate conditions designed to ensure that individuals to whom the product is
administered are informed
(I) that the Secretary has authorized the emergency use of the product;
(II) of the significant known and potential benefits and risks of such use, and of the extent to
which such benefits and risks are unknown; and
(III) of the option to accept or refuse administration of the product, of the consequences, if any,
of refusing administration of the product, and of the alternatives to the product that are
available and of their benefits and risks.
(iii) Appropriate conditions for the monitoring and reporting of adverse events associated with
the emergency use of the product.
(iv) For manufacturers of the product, appropriate conditions concerning recordkeeping and
reporting, including records access by the Secretary, with respect to the emergency use of the
product.
(B) Authority for additional conditions. With respect to the emergency use of an unapproved
product, the Secretary may, for a person who carries out any activity for which the
authorization is issued, establish such conditions on an authorization under this section as the
Secretary finds necessary or appropriate to protect the public health, including the following:
(i) Appropriate conditions on which entities may distribute the product with respect to the
emergency use of the product (including limitation to distribution by government entities), and
on how distribution is to be performed.
(ii) Appropriate conditions on who may administer the product with respect to the emergency
use of the product, and on the categories of individuals to whom, and the circumstances under
which, the product may be administered with respect to such use.
(iii) Appropriate conditions with respect to the collection and analysis of information, during the
period when the authorization is in effect, concerning the safety and effectiveness of the
product with respect to the emergency use of such product.
(iv) For persons other than manufacturers of the product, appropriate conditions concerning
recordkeeping and reporting, including records access by the Secretary, with respect to the
emergency use of the product.
(2) Unapproved use. With respect to the emergency use of a product that is an unapproved
use of an approved product:
(A) For a manufacturer of the product who carries out any activity for which the authorization is
issued, the Secretary shall, to the extent practicable given the circumstances of the
emergency, establish conditions described in clauses (i) and (ii) of paragraph (1)(A), and may
establish conditions described in clauses (iii) and (iv) of such paragraph.
(B)(i) If the authorization under this section regarding the emergency use authorizes a change
in the labeling of the product, but the manufacturer of the product chooses not to make such
change, such authorization may not authorize distributors of the product or any other person to
alter or obscure the labeling provided by the manufacturer.
(ii) In the circumstances described in clause (i), for a person who does not manufacture the
product and who chooses to act under this clause, an authorization under this section
regarding the emergency use shall, to the extent practicable given the circumstances of the
emergency, authorize such person to provide appropriate information with respect to such
product in addition to the labeling provided by the manufacturer, subject to compliance with
clause (i). While the authorization under this section is effective, such additional information
shall not be considered labeling for purposes of section 502.
(C) The Secretary may establish with respect to the distribution and administration of the
product for the unapproved use conditions no more restrictive than those established by the
Secretary with respect to the distribution and administration of the product for the approved
use.
(3) Good manufacturing practice. With respect to the emergency use of a product for which an
authorization under this section is issued (whether an unapproved product or an unapproved
use of an approved product), the Secretary may waive or limit, to the extent appropriate given
the circumstances of the emergency, requirements regarding current good manufacturing
practice otherwise applicable to the manufacture, processing, packing, or holding of products
subject to regulation under this Act, including such requirements established under section
501.
(4) Advertising. The Secretary may establish conditions on advertisements and other
promotional descriptive printed matter that relate to the emergency use of a product for which
an authorization under this section is issued (whether an unapproved product or an
unapproved use of an approved product), including, as appropriate
(A) with respect to drugs and biological products, requirements applicable to prescription drugs
pursuant to section 502(n); or
(B) with respect to devices, requirements applicable to restricted devices pursuant to section
502(r).
(f) Duration of Authorization.
(1) In general. Except as provided in paragraph (2), an authorization under this section shall be
effective until the earlier of the termination of the declaration under subsection (b) or a
revocation under subsection (g).
(2) Continued use after end of effective period. Notwithstanding the termination of the
declaration under subsection (b) or a revocation under subsection (g), an authorization shall
continue to be effective to provide for continued use of an unapproved product with respect to
a patient to whom it was administered during the period described by paragraph (1), to the
extent found necessary by such patient's attending physician.
(g) Revocation of Authorization.
(1) Review. The Secretary shall periodically review the circumstances and the appropriateness
of an authorization under this section.
(2) Revocation. The Secretary may revoke an authorization under this section if the criteria
under subsection (c) for issuance of such authorization are no longer met or other
circumstances make such revocation appropriate to protect the public health or safety.
(h) Publication; Confidential Information.
(1) Publication. The Secretary shall promptly publish in the Federal Register a notice of each
authorization, and each termination or revocation of an authorization under this section, and
an explanation of the reasons therefore (which may include a summary of data or information
that has been submitted to the Secretary in an application under section 505(i) or section
520(g), even if such summary may indirectly reveal the existence of such application).
(2) Confidential information. Nothing in this section alters or amends section 1905 of title 18,
United States Code, or section 552(b)(4) of title 5 of such Code.
(i) Actions Committed to Agency Discretion. Actions under the authority of this section by the
Secretary or by the Secretary of Defense are committed to agency discretion.
(j) Rules of Construction. The following applies with respect to this section:
(1) Nothing in this section impairs the authority of the President as Commander in Chief of the
Armed Forces of the United States under article II, section 2 of the United States Constitution.
(2) Nothing in this section impairs the authority of the Secretary of Defense with respect to the
Department of Defense, including the armed forces, under other provisions of Federal law.
(3) Nothing in this section (including any exercise of authority by a manufacturer under
subsection (e)(2)) impairs the authority of the United States to use or manage quantities of a
product that are owned or controlled by the United States (including quantities in the stockpile
maintained under section 319F-2 of the Public Health Service Act).
(k) Relation to Other Provisions. If a product is the subject of an authorization under this
section, the use of such product within the scope of the authorization shall not be considered
to constitute a clinical investigation for purposes of section 505(i), section 520(g), or any other
provision of this Act or section 351 of the Public Health Service Act.
(l) Option to Carry Out Authorized Activities. Nothing in this section provides the Secretary any
authority to require any person to carry out any activity that becomes lawful pursuant to an
authorization under this section, and no person is required to inform the Secretary that the
person will not be carrying out such activity, except that a manufacturer of a sole-source
unapproved product authorized for emergency use shall report to the Secretary within a
reasonable period of time after the issuance by the Secretary of such authorization if such
manufacturer does not intend to carry out any activity under the authorization. This section
only has legal effect on a person who carries out an activity for which an authorization under
this section is issued. This section does not modify or affect activities carried out pursuant to
other provisions of this Act or section 351 of the Public Health Service Act. Nothing in this
subsection may be construed as restricting the Secretary from imposing conditions on persons
who carry out any activity pursuant to an authorization under this section.
SEC. 565 [21 USC § 360bbb-4] TECHNICAL ASSISTANCE.
The Secretary, in consultation with the Commissioner of Food and Drugs, shall establish within
the Food and Drug Administration a team of experts on manufacturing and regulatory activities
(including compliance with current Good Manufacturing Practice) to provide both off-site and
on-site technical assistance to the manufacturers of qualified countermeasures (as defined in
section 319F-1 of the Public Health Service Act [42 USC § 247d-6a]), security
countermeasures (as defined in section 319F-2 of such Act [42 USC § 247d-6b]), or vaccines,
at the request of such a manufacturer and at the discretion of the Secretary, if the Secretary
determines that a shortage or potential shortage may occur in the United States in the supply
of such vaccines or countermeasures and that the provision of such assistance would be
beneficial in helping alleviate or avert such shortage.
CHAPTER V--Drugs and Devices Subchapter F--New Animal Drugs for Minor Use and Minor Species
SEC. 571. 1 [21 U.S.C. 360ccc] CONDITIONAL APPROVAL OF NEW ANIMAL DRUGS FOR
MINOR USE AND MINOR SPECIES.
(a)(1) Except as provided in paragraph (3) of this section, any person may file with the
Secretary an application for conditional approval of a new animal drug intended for a minor
use or a minor species. Such an application may not be a supplement to an application
approved under section 512. Such application must comply in all respects with the provisions
of section 512 of this Act except sections 512(a)(4), 512(b)(2), 512(c)(1), 512(c)(2), 512(c)(3),
512(d)(1), 512(e), 512(h), and 512(n) unless otherwise stated in this section, and any
additional provisions of this section. New animal drugs are subject to application of the same
safety standards that would be applied to such drugs under section 512(d) (including, for
antimicrobial new animal drugs, with respect to antimicrobial resistance).
(2) The applicant shall submit to the Secretary as part of an application for the conditional
approval of a new animal drug—
(A) all information necessary to meet the requirements of section 512(b)(1) except section
512(b)(1)(A);
(B) full reports of investigations which have been made to show whether or not such drug is
safe under section 512(d) (including, for an antimicrobial new animal drug, with respect to
antimicrobial resistance) and there is a reasonable expectation of effectiveness for use;
(C) data for establishing a conditional dose;
(D) projections of expected need and the justification for that expectation based on the best
information available;
(E) information regarding the quantity of drug expected to be distributed on an annual basis to
meet the expected need; and
(F) a commitment that the applicant will conduct additional investigations to meet the
requirements for the full demonstration of effectiveness under section 512(d)(1)(E) within 5
years.
(3) A person may not file an application under paragraph (1) if—
(A) the application seeks conditional approval of a new animal drug that is contained in, or is a
product of, a transgenic animal.
(B) the person has previously filed an application for conditional approval under paragraph (1)
for the same drug in the same dosage form for the same intended use whether or not
subsequently conditionally approved by the Secretary under subsection (b), or
(C) the person obtained the application, or data or other information contained therein, directly
or indirectly from the person who filed for conditional approval under paragraph (1) for the
same drug in the same dosage form for the same intended use whether or not subsequently
conditionally approved by the Secretary under subsection (b).
(b) Within 180 days after the filing of an application pursuant to subsection (a), or such
additional period as may be agreed upon by the Secretary and the applicant, the Secretary
shall either—
(1) issue an order, effective for one year, conditionally approving the application if the
Secretary finds that none of the grounds for denying conditional approval, specified in
subsection (c) of this section applies and publish a Federal Register notice of the conditional
approval, or
(2) give the applicant notice of an opportunity for an informal hearing on the question whether
such application can be conditionally approved.
(c) If the Secretary finds, after giving the applicant notice and an opportunity for an informal
hearing, that—
(1) any of the provisions of section 512(d)(1) (A) through (D) or (F) through (I) are applicable;
(2) the information submitted to the Secretary as part of the application and any other
information before the Secretary with respect to such drug, is insufficient to show that there is
a reasonable expectation that the drug will have the effect it purports or is represented to have
under the conditions of use prescribed, recommended, or suggested in the proposed labeling
thereof; or
(3) another person has received approval under section 512 for the same drug in the same
dosage form for the same intended use, and that person is able to assure the availability of
sufficient quantities of the drug to meet the needs for which the drug is intended;
the Secretary shall issue an order refusing to conditionally approve the application. If, after
such notice and opportunity for an informal hearing, the Secretary finds that paragraphs (1)
through (3) do not apply, the Secretary shall issue an order conditionally approving the
application effective for one year and publish a Federal Register notice of the conditional
approval. Any order issued under this subsection refusing to conditionally approve an
application shall state the findings upon which it is based.
(d) A conditional approval under this section is effective for a 1-year period and is thereafter
renewable by the Secretary annually for up to 4 additional 1-year terms. A conditional approval
shall be in effect for no more than 5 years from the date of approval under subsection (b)(1) or
(c) of this section unless extended as provided for in subsection (h) of this section. The
following shall also apply:
(1) No later than 90 days from the end of the 1-year period for which the original or renewed
conditional approval is effective, the applicant may submit a request to renew a conditional
approval for an additional 1-year term.
(2) A conditional approval shall be deemed renewed at the end of the 1-year period, or at the
end of a 90-day extension that the Secretary may, at the Secretary’s discretion, grant by letter
in order to complete review of the renewal request, unless the Secretary determines before the
expiration of the 1-year period or the 90-day extension that—
(A) the applicant failed to submit a timely renewal request;
(B) the request fails to contain sufficient information to show that—
(i) the applicant is making sufficient progress toward meeting approval requirements under
section 512(d)(1)(E), and is likely to be able to fulfill those requirements and obtain an
approval under section 512 before the expiration of the 5-year maximum term of the
conditional approval;
(ii) the quantity of the drug that has been distributed is consistent with the conditionally
approved intended use and conditions of use, unless there is adequate explanation that
ensures that the drug is only used for its intended purpose; or
(iii) the same drug in the same dosage form for the same intended use has not received
approval under section 512, or if such a drug has been approved, that the holder of the
approved application is unable to assure the availability of sufficient quantities of the drug to
meet the needs for which the drug is intended; or
(C) any of the provisions of section 512(e)(1) (A) through (B) or (D) through (F) are applicable.
(3) If the Secretary determines before the end of the 1-year period or the 90-day extension, if
granted, that a conditional approval should not be renewed, the Secretary shall issue an order
refusing to renew the conditional approval, and such conditional approval shall be deemed
withdrawn and no longer in effect. The Secretary shall thereafter provide an opportunity for an
informal hearing to the applicant on the issue whether the conditional approval shall be
reinstated.
(e)(1) The Secretary shall issue an order withdrawing conditional approval of an application
filed pursuant to subsection (a) if the Secretary finds that another person has received
approval under section 512 for the same drug in the same dosage form for the same intended
use and that person is able to assure the availability of sufficient quantities of the drug to meet
the needs for which the drug is intended.
(2) The Secretary shall, after due notice and opportunity for an informal hearing to the
applicant, issue an order withdrawing conditional approval of an application filed pursuant to
subsection (a) if the Secretary finds that—
(A) any of the provisions of section 512(e)(1) (A) through (B) or (D) through (F) are applicable;
or
(B) on the basis of new information before the Secretary with respect to such drug, evaluated
together with the evidence available to the Secretary when the application was conditionally
approved, that there is not a reasonable expectation that such drug will have the effect it
purports or is represented to have under the conditions of use prescribed, recommended, or
suggested in the labeling thereof.
(3) The Secretary may also, after due notice and opportunity for an informal hearing to the
applicant, issue an order withdrawing conditional approval of an application filed pursuant to
subsection (a) if the Secretary finds that any of the provisions of section 512(e)(2) are
applicable.
(f)(1) The label and labeling of a new animal drug with a conditional approval under this section
shall—
(A) bear the statement, "conditionally approved by FDA pending a full demonstration of
effectiveness under application number"; and
(B) contain such other information as prescribed by the Secretary.
(2) An intended use that is the subject of a conditional approval under this section shall not be
included in the same product label with any intended use approved under section 512.
(g) A conditionally approved new animal drug application may not be amended or
supplemented to add indications for use.
(h) 180 days prior to the termination date established under subsection (d) of this section, an
applicant shall have submitted all the information necessary to support a complete new animal
drug application in accordance with section 512(b)(1) or the conditional approval issued under
this section is no longer in effect. Following review of this information, the Secretary shall
either—
(1) issue an order approving the application under section 512(c) if the Secretary finds that
none of the grounds for denying approval specified in section 512(d)(1) applies, or
(2) give the applicant an opportunity for a hearing before the Secretary under section 512(d)
on the question whether such application can be approved.
Upon issuance of an order approving the application, product labeling and administrative
records of approval shall be modified accordingly. If the Secretary has not issued an order
under section 512(c) approving such application prior to the termination date established
under subsection (d) of this section, the conditional approval issued under this section is no
longer in effect unless the Secretary grants an extension of an additional 180-day period so
that the Secretary can complete review of the application. The decision to grant an extension
is committed to the discretion of the Secretary and not subject to judicial review.
(i) The decision of the Secretary under subsection (c), (d), or (e) of this section refusing or
withdrawing conditional approval of an application shall constitute final agency action subject
to judicial review.
(j) In this section and section 572, the term "transgenic animal" means an animal whose
genome contains a nucleotide sequence that has been intentionally modified in vitro, and the
progeny of such an animal; Provided that the term "transgenic animal" does not include an
animal of which the nucleotide sequence of the genome has been modified solely by selective
breeding.
SEC. 572. 2 [21 U.S.C. 360ccc-1] INDEX OF LEGALLY MARKETED UNAPPROVED NEW
ANIMAL DRUGS FOR MINOR SPECIES.
(a)(1) The Secretary shall establish an index limited to—
(A) new animal drugs intended for use in a minor species for which there is a reasonable
certainty that the animal or edible products from the animal will not be consumed by humans or
food-producing animals; and
(B) new animal drugs intended for use only in a hatchery, tank, pond, or other similar
contained man-made structure in an early, non-food life stage of a food-producing minor
species, where safety for humans is demonstrated in accordance with the standard of section
512(d) (including, for an antimicrobial new animal drug, with respect to antimicrobial
resistance).
(2) The index shall not include a new animal drug that is contained in or a product of a
transgenic animal.
(b) Any person intending to file a request under this section shall be entitled to one or more
conferences to discuss the requirements for indexing a new animal drug.
(c)(1) Any person may submit a request to the Secretary for a determination whether a new
animal drug may be eligible for inclusion in the index. Such a request shall include—
(A) information regarding the need for the new animal drug, the species for which the new
animal drug is intended, the proposed intended use and conditions of use, and anticipated
annual distribution;
(B) information to support the conclusion that the proposed use meets the conditions of
subparagraph (A) or (B) of subsection (a)(1) of this section;
(C) information regarding the components and composition of the new animal drug;
(D) a description of the methods used in, and the facilities and controls used for, the
manufacture, processing, and packing of such new animal drug;
(E) an environmental assessment that meets the requirements of the National Environmental
Policy Act of 1969, as amended, and as defined in 21 CFR Part 25, as it appears on the date
of enactment of this provision 3 and amended thereafter or information to support a categorical
exclusion from the requirement to prepare an environmental assessment;
(F) information sufficient to support the conclusion that the proposed use of the new animal
drug is safe under section 512(d) with respect to individuals exposed to the new animal drug
through its manufacture or use; and
(G) such other information as the Secretary may deem necessary to make this eligibility
determination.
(2) Within 90 days after the submission of a request for a determination of eligibility for
indexing based on subsection (a)(1)(A) of this section, or 180 days for a request submitted
based on subsection (a)(1)(B) of this section, the Secretary shall grant or deny the request,
and notify the person who requested such determination of the Secretary's decision. The
Secretary shall grant the request if the Secretary finds that—
(A) the same drug in the same dosage form for the same intended use is not approved or
conditionally approved;
(B) the proposed use of the drug meets the conditions of subparagraph (A) or (B) of subsection
(a)(1), as appropriate;
(C) the person requesting the determination has established appropriate specifications for the
manufacture and control of the new animal drug and has demonstrated an understanding of
the requirements of current good manufacturing practices;
(D) the new animal drug will not significantly affect the human environment; and
(E) the new animal drug is safe with respect to individuals exposed to the new animal drug
through its manufacture or use.
If the Secretary denies the request, the Secretary shall thereafter provide due notice and an
opportunity for an informal conference. A decision of the Secretary to deny an eligibility
request following an informal conference shall constitute final agency action subject to judicial
review.
(d)(1) With respect to a new animal drug for which the Secretary has made a determination of
eligibility under subsection (c), the person who made such a request may ask that the
Secretary add the new animal drug to the index established under subsection (a). The request
for addition to the index shall include—
(A) a copy of the Secretary's determination of eligibility issued under subsection (c);
(B) a written report that meets the requirements in subsection (d)(2) of this section;
(C) a proposed index entry;
(D) facsimile labeling;
(E) anticipated annual distribution of the new animal drug;
(F) a written commitment to manufacture the new animal drug and animal feeds bearing or
containing such new animal drug according to current good manufacturing practices;
(G) a written commitment to label, distribute, and promote the new animal drug only in
accordance with the index entry;
(H) upon specific request of the Secretary, information submitted to the expert panel described
in paragraph (3); and
(I) any additional requirements that the Secretary may prescribe by general regulation or
specific order.
(2) The report required in paragraph (1) shall—
(A) be authored by a qualified expert panel;
(B) include an evaluation of all available target animal safety and effectiveness information,
including anecdotal information;
(C) state the expert panel's opinion regarding whether the benefits of using the new animal
drug for the proposed use in a minor species outweigh its risks to the target animal, taking into
account the harm being caused by the absence of an approved or conditionally approved new
animal drug for the minor species in question;
(D) include information from which labeling can be written; and
(E) include a recommendation regarding whether the new animal drug should be limited to use
under the professional supervision of a licensed veterinarian.
(3) A qualified expert panel, as used in this section, is a panel that—
(A) is composed of experts qualified by scientific training and experience to evaluate the target
animal safety and effectiveness of the new animal drug under consideration;
(B) operates external to FDA 4 ; and
(C) is not subject to the Federal Advisory Committee Act, 5 U.S.C. App. 2.
The Secretary shall define the criteria for selection of a qualified expert panel and the
procedures for the operation of the panel by regulation.
(4) Within 180 days after the receipt of a request for listing a new animal drug in the index, the
Secretary shall grant or deny the request. The Secretary shall grant the request if the request
for indexing continues to meet the eligibility criteria in subsection (a) and the Secretary finds,
on the basis of the report of the qualified expert panel and other information available to the
Secretary, that the benefits of using the new animal drug for the proposed use in a minor
species outweigh its risks to the target animal, taking into account the harm caused by the
absence of an approved or conditionally-approved new animal drug for the minor species in
question. If the Secretary denies the request, the Secretary shall thereafter provide due notice
and the opportunity for an informal conference. The decision of the Secretary following an
informal conference shall constitute final agency action subject to judicial review.
(e)(1) The index established under subsection (a) shall include the following information for
each listed drug—
(A) the name and address of the person who holds the index listing;
(B) the name of the drug and the intended use and conditions of use for which it is being
indexed;
(C) product labeling; and
(D) conditions and any limitations that the Secretary deems necessary regarding use of the
drug.
(2) The Secretary shall publish the index, and revise it periodically.
(3) The Secretary may establish by regulation a process for reporting changes in the
conditions of manufacturing or labeling of indexed products.
(f)(1) If the Secretary finds, after due notice to the person who requested the index listing and
an opportunity for an informal conference, that—
(A) the expert panel failed to meet the requirements as set forth by the Secretary by regulation;
(B) on the basis of new information before the Secretary, evaluated together with the evidence
available to the Secretary when the new animal drug was listed in the index, the benefits of
using the new animal drug for the indexed use do not outweigh its risks to the target animal;
(C) the conditions of subsection (c)(2) of this section are no longer satisfied;
(D) the manufacture of the new animal drug is not in accordance with current good
manufacturing practices;
(E) the labeling, distribution, or promotion of the new animal drug is not in accordance with the
index entry;
(F) the conditions and limitations of use associated with the index listing have not been
followed; or
(G) the request for indexing contains any untrue statement of material fact,
the Secretary shall remove the new animal drug from the index. The decision of the Secretary
following an informal conference shall constitute final agency action subject to judicial review.
(2) If the Secretary finds that there is a reasonable probability that the use of the drug would
present a risk to the health of humans or other animals, the Secretary may—
(A) suspend the listing of such drug immediately;
(B) give the person listed in the index prompt notice of the Secretary's action; and
(C) afford that person the opportunity for an informal conference.
The decision of the Secretary following an informal conference shall constitute final agency
action subject to judicial review.
(g) For purposes of indexing new animal drugs under this section, to the extent consistent with
the public health, the Secretary shall promulgate regulations for exempting from the operation
of section 512 minor species new animal drugs and animal feeds bearing or containing new
animal drugs intended solely for investigational use by experts qualified by scientific training
and experience to investigate the safety and effectiveness of minor species animal drugs.
Such regulations may, at the discretion of the Secretary, among other conditions relating to the
protection of the public health, provide for conditioning such exemption upon the establishment
and maintenance of such records, and the making of such reports to the Secretary, by the
manufacturer or the sponsor of the investigation of such article, of data (including but not
limited to analytical reports by investigators) obtained as a result of such investigational use of
such article, as the Secretary finds will enable the Secretary to evaluate the safety and
effectiveness of such article in the event of the filing of a request for an index listing pursuant to
this section.
(h) The labeling of a new animal drug that is the subject of an index listing shall state,
prominently and conspicuously—
(1) "NOT APPROVED BY FDA.—Legally marketed as an FDA indexed product. Extra-label
use is prohibited.";
(2) except in the case of new animal drugs indexed for use in an early life stage of a
food-producing animal, "This product is not to be used in animals intended for use as food for
humans or other animals."; and
(3) such other information as may be prescribed by the Secretary in the index listing.
(i)(1) In the case of any new animal drug for which an index listing pursuant to subsection (a) is
in effect, the person who has an index listing shall establish and maintain such records, and
make such reports to the Secretary, of data relating to experience, and other data or
information, received or otherwise obtained by such person with respect to such drug, or with
respect to animal feeds bearing or containing such drug, as the Secretary may by general
regulation, or by order with respect to such listing, prescribe on the basis of a finding that such
records and reports are necessary in order to enable the Secretary to determine, or facilitate a
determination, whether there is or may be ground for invoking subsection (f). Such regulation
or order shall provide, where the Secretary deems it to be appropriate, for the examination,
upon request, by the persons to whom such regulation or order is applicable, of similar
information received or otherwise obtained by the Secretary.
(2) Every person required under this subsection to maintain records, and every person in
charge or custody thereof, shall, upon request of an officer or employee designated by the
Secretary, permit such officer or employee at all reasonable times to have access to and copy
and verify such records.
(j)(1) Safety and effectiveness data and information which has been submitted in support of a
request for a new animal drug to be indexed under this section and which has not been
previously disclosed to the public shall be made available to the public, upon request, unless
extraordinary circumstances are shown—
(A) if no work is being or will be undertaken to have the drug indexed in accordance with the
request,
(B) if the Secretary has determined that such drug cannot be indexed and all legal appeals
have been exhausted,
(C) if the indexing of such drug is terminated and all legal appeals have been exhausted, or
(D) if the Secretary has determined that such drug is not a new animal drug.
(2) Any request for data and information pursuant to paragraph (1) shall include a verified
statement by the person making the request that any data or information received under such
paragraph shall not be disclosed by such person to any other person—
(A) for the purpose of, or as part of a plan, scheme, or device for, obtaining the right to make,
use, or market, or making, using, or marketing, outside the United States, the drug identified in
the request for indexing; and
(B) without obtaining from any person to whom the data and information are disclosed an
identical verified statement, a copy of which is to be provided by such person to the Secretary,
which meets the requirements of this paragraph.
SEC. 573. 5 [21 U.S.C. 360ccc-2] DESIGNATED NEW ANIMAL DRUGS FOR MINOR USE
OR MINOR SPECIES.
(a) DESIGNATION.—
(1) The manufacturer or the sponsor of a new animal drug for a minor use or use in a minor
species may request that the Secretary declare that drug a "designated new animal drug". A
request for designation of a new animal drug shall be made before the submission of an
application under section 512(b) or section 571 for the new animal drug.
(2) The Secretary may declare a new animal drug a "designated new animal drug" if—
(A) it is intended for a minor use or use in a minor species; and
(B) the same drug in the same dosage form for the same intended use is not approved under
section 512 or 571 or designated under this section at the time the request is made.
(3) Regarding the termination of a designation—
(A) the sponsor of a new animal drug shall notify the Secretary of any decision to discontinue
active pursuit of approval under section 512 or 571 of an application for a designated new
animal drug. The Secretary shall terminate the designation upon such notification;
(B) the Secretary may also terminate designation if the Secretary independently determines
that the sponsor is not actively pursuing approval under section 512 or 571 with due diligence;
(C) the sponsor of an approved designated new animal drug shall notify the Secretary of any
discontinuance of the manufacture of such new animal drug at least one year before
discontinuance. The Secretary shall terminate the designation upon such notification; and
(D) the designation shall terminate upon the expiration of any applicable exclusivity period
under subsection (c).
(4) Notice respecting the designation or termination of designation of a new animal drug shall
be made available to the public.
(b) GRANTS AND CONTRACTS FOR DEVELOPMENT OF DESIGNATED NEW ANIMAL
DRUGS.—
(1) The Secretary may make grants to and enter into contracts with public and private entities
and individuals to assist in defraying the costs of qualified safety and effectiveness testing
expenses and manufacturing expenses incurred in connection with the development of
designated new animal drugs.
(2) For purposes of paragraph (1) of this section—
(A) The term ‘qualified safety and effectiveness testing’ means testing—
(i) which occurs after the date such new animal drug is designated under this section and
before the date on which an application with respect to such drug is submitted under section
512; and
(ii) which is carried out under an investigational exemption under section 512(j).
(B) The term "manufacturing expenses" means expenses incurred in developing processes
and procedures associated with manufacture of the designated new animal drug which occur
after the new animal drug is designated under this section and before the date on which an
application with respect to such new animal drug is submitted under section 512 or 571.
(c) EXCLUSIVITY FOR DESIGNATED NEW ANIMAL DRUGS.—
(1) Except as provided in subsection (c)(2), if the Secretary approves or conditionally approves
an application for a designated new animal drug, the Secretary may not approve or
conditionally approve another application submitted for such new animal drug with the same
intended use as the designated new animal drug for another applicant before the expiration of
seven years from the date of approval or conditional approval of the application.
(2) If an application filed pursuant to section 512 or section 571 is approved for a designated
new animal drug, the Secretary may, during the 7-year exclusivity period beginning on the date
of the application approval or conditional approval, approve or conditionally approve another
application under section 512 or section 571 for such drug for such minor use or minor species
for another applicant if—
(A) the Secretary finds, after providing the holder of such an approved application notice and
opportunity for the submission of views, that in the granted exclusivity period the holder of the
approved application cannot assure the availability of sufficient quantities of the drug to meet
the needs for which the drug was designated; or
(B) such holder provides written consent to the Secretary for the approval or conditional
approval of other applications before the expiration of such exclusivity period.
Footnotes: Chapter V, Subchapter F
1. This subchapter, consisting of sections 571 through 573, was added by section 102(b)(4) of
Public Law 108–282. Section 102(b)(6) of the Public Law concerns regulations to implement
sections 571 through 573 and is included in the appendix to this compiliation under the
heading "Section 102(b)(6) of Minor Use and Minor Species Animal Health Act of 2004".
2. See footnote for section 571.
3. Provision was added by section 102(b)(4) of Public Law 108–282, which was enacted
August
2, 2004.
4. So in law. See section 102(b)(4) of Public Law 108-282. Probably should be "the Food and
Drug Administration".
5. See footnote for section 571.
CHAPTER VI —COSMETICS
ADULTERATED COSMETICS
SEC. 601. [21 U.S.C. 361] A cosmetic shall be deemed to be adulterated— 1
(a) If it bears or contains any poisonous or deleterious substance which may render it injurious
to users under the conditions of use prescribed in the labeling thereof, or, under such
conditions of use as are customary or usual, except that this provision shall not apply to
coal-tar hair dye, the label of which bears the following legend conspicuously displayed
thereon: ‘‘Caution—This product contains ingredients which may cause skin irritation on
certain individuals and a preliminary test according to accompanying directions should first be
made. This product must not be used for dyeing the eyelashes or eyebrows; to do so may
cause blindness.’’, and the labeling of which bears adequate directions for such preliminary
testing. For the purposes of this paragraph and paragraph (e) the term ‘‘hair dye’’ shall not
include eyelash dyes or eyebrow dyes.
(b) If it consists in whole or in part of any filthy, putrid, or decomposed substance.
(c) If it has been prepared, packed, or held under insanitary conditions whereby it may have
become contaminated with filth, or whereby it may have been rendered injurious to health.
(d) If its container is composed, in whole or in part, of any poisonous or deleterious substance
which may render the contents injurious to health.
(e) If it is not a hair dye and it is, or it bears or contains, a color additive which is unsafe within
the meaning of section 721(a).
MISBRANDED COSMETICS
SEC. 602. [21 U.S.C. 362] A cosmetic shall be deemed to be misbranded—
(a) If its labeling is false or misleading in any particular.
(b) If in package form unless it bears a label containing (1) the name and place of business of
the manufacturer, packer, or distributor; and (2) an accurate statement of the quantity of the
contents in terms of weight, measure, or numerical count: Provided, That under clause (2) of
this paragraph reasonable variations shall be permitted, and exemptions as to small packages
shall be established, by regulations prescribed by the Secretary.
(c) If any word, statement, or other information required by or under authority of this Act to
appear on the label or labeling is not prominently placed thereon with such conspicuousness
(as compared with other words, statements, designs, or devices in the labeling) and in such
terms as to render it likely to be read and understood by the ordinary individual under
customary conditions of purchase and use.
(d) If its container is so made, formed, or filled as to be misleading.
(e) If it is a color additive, unless its packaging and labeling are in conformity with such
packaging and labeling requirements, applicable to such color additive, as may be contained
in regulations issued under section 721. This paragraph shall not apply to packages of color
additives which, with respect to their use for cosmetics, are marketed and intended for use
only in or on hair dyes (as defined in the last sentence of section 601(a)).
(f) If its packaging or labeling is in violation of an applicable regulation issued pursuant to
section 3 or 4 of the Poison Prevention Packaging Act of 1970.
REGULATIONS MAKING EXEMPTIONS
SEC. 603 . [21 U.S.C. 363] The Secretary shall promulgate regulations exempting from any
labeling requirement of this Act cosmetics which are, in accordance with the practice of the
trade, to be processed, labeled, or repacked in substantial quantities at establishments other
than those where originally processed or packed, on condition that such cosmetics are not
adulterated or misbranded under the provisions of this Act upon removal from such processing,
labeling, or repacking establishment.
Footnotes: Chapter VI
1. See footnote for section 403(h)(3) regarding the stylistic use of a list consisting of "(a)",
"(b)", etc.
CHAPTER VII—GENERAL AUTHORITY SUBCHAPTER A--GENERAL ADMINISTRATIVE PROVISIONS
REGULATIONS AND HEARINGS
SEC. 701. [21 U.S.C. 371] (a) The authority to promulgate regulations for the efficient
enforcement of this Act, except as otherwise provided in this section, is hereby vested in the
Secretary.
(b) The Secretary of the Treasury and the Secretary of Health and Human Services shall
jointly prescribe regulations for the efficient enforcement of the provisions of section 801,
except as otherwise provided therein. Such regulations shall be promulgated in such manner
and take effect at such time, after due notice, as the Secretary of Health and Human Services
shall determine.
(c) Hearings authorized or required by this Act shall be conducted by the Secretary or such
officer or employee as he may designate for the purpose.
(d) The definitions and standards of identity promulgated in accordance with the provisions of
this Act shall be effective for the purposes of the enforcement of this Act, notwithstanding such
definitions and standards as may be contained in other laws of the United States and
regulations promulgated thereunder.
(e)(1) Any action for the issuance, amendment, or repeal of any regulation under section 403(j),
404(a), 406, 501(b), or 502 (d) or (h) of this Act, and any action for the amendment or repeal of
any definition and standard of identity under section 401 of this Act for any dairy product
(including products regulated under parts 131, 133 and 135 of title 21, Code of Federal
Regulations) or maple sirup (regulated under section 168.140 of title 21, Code of Federal
Regulations) 1 shall be begun by a proposal made (A) by the Secretary on his own initiative, or
(B) by petition of any interested persons, showing reasonable grounds therefor, filed with the
Secretary. The Secretary shall publish such proposal and shall afford all interested persons an
opportunity to present their views thereon, orally or in writing. As soon as practicable thereafter,
the Secretary shall by order act upon such proposal and shall make such order public. Except
as provided in paragraph (2), the order shall become effective at such time as may be
specified therein, but not prior to the day following the last day on which objections may be
filed under such paragraph.
(2) On or before the thirtieth day after the date on which an order entered under paragraph (1)
is made public, any person who will be adversely affected by such order if placed in effect may
file objections thereto with the Secretary, specifying with particularity the provisions of the
order deemed objectionable, stating the grounds therefor, and requesting a public hearing
upon such objections. Until final action upon such objections is taken by the Secretary under
paragraph (3), the filing of such objections shall operate to stay the effectiveness of those
provisions of the order to which the objections are made. As soon as practicable after the time
for filing objections has expired the Secretary shall publish a notice in the Federal Register
specifying those parts of the order which have been stayed by the filing of objections and, if no
objections have been filed, stating that fact.
(3) As soon as practicable after such request for a public hearing, the Secretary, after due
notice, shall hold such a public hearing for the purpose of receiving evidence relevant and
material to the issues raised by such objections. At the hearing, any interested person may be
heard in person or by representative. As soon as practicable after completion of the hearing,
the Secretary shall by order act upon such objections and make such order public. Such order
shall be based only on substantial evidence of record at such hearing and shall set forth, as
part of the order, detailed findings of fact on which the order is based. The Secretary shall
specify in the order the date on which it shall take effect, except that it shall not be made to
take effect prior to the ninetieth day after its publication unless the Secretary finds that
emergency conditions exist necessitating an earlier effective date, in which event the
Secretary shall specify in the order his findings as to such conditions.
(f)(1) In a case of actual controversy as to the validity of any order under subsection (e), any
person who will be adversely affected by such order if placed in effect may at any time prior to
the ninetieth day after such order is issued file a petition with the Circuit Court of Appeals of the
United States for the circuit wherein such person resides or has his principal place of business,
for a judicial review of such order. A copy of the petition shall be forthwith transmitted by the
clerk of the court to the Secretary or other officer designated by him for that purpose. The
Secretary thereupon shall file in the court the record of the proceedings on which the Secretary
based his order, as provided in section 2112 of title 28, United States Code.
(2) If the petitioner applies to the court for leave to adduce additional evidence, and shows to
the satisfaction of the court that such additional evidence is material and that there were
reasonable grounds for the failure to adduce such evidence in the proceeding before the
Secretary the court may order such additional evidence (and evidence in rebuttal thereof) to be
taken before the Secretary, and to be adduced upon the hearing, in such manner and upon
such terms and conditions as to the court may seem proper. The Secretary may modify his
findings as to the facts, or make new findings, by reason of the additional evidence, so taken,
and he shall file such modified or new findings, and his recommendation, if any, for the
modification or setting aside of his original order, with the return of such additional evidence.
(3) Upon the filing of the petition referred to in paragraph (1) of this subsection, the court shall
have jurisdiction to affirm the order, or to set it aside in whole or in part, temporarily or
permanently. If the order of the Secretary refuses to issue, amend, or repeal a regulation and
such order is not in accordance with law the court shall by its judgment order the Secretary to
take action with respect to such regulation, in accordance with law. The findings of the
Secretary as to the facts, if supported by substantial evidence, shall be conclusive.
(4) The judgment of the court affirming or setting aside, in whole or in part, any such order of
the Secretary shall be final, subject to review by the Supreme Court of the United States upon
certiorari or certification as provided in section 1254 of title 28, United States Code.
(5) Any action instituted under this subsection shall survive notwithstanding any change in the
person occupying the office of Secretary or any vacancy in such office.
(6) The remedies provided for in this subsection shall be in addition to and not in substitution
for any other remedies provided by law.
(g) A certified copy of the transcript of the record and proceedings under subsection (e) shall
be furnished by the Secretary to any interested party at his request, and payment of the costs
thereof, and shall be admissible in any criminal libel for condemnation, exclusion of imports, or
other proceeding arising under or in respect of this Act, irrespective of whether proceedings
with respect to the order have previously been instituted or become final under subsection (f).
(h)(1)(A) The Secretary shall develop guidance documents with public participation and
ensure that information identifying the existence of such documents and the documents
themselves are made available to the public both in written form and, as feasible, through
electronic means. Such documents shall not create or confer any rights for or on any person,
although they present the views of the Secretary on matters under the jurisdiction of the Food
and Drug Administration.
(B) Although guidance documents shall not be binding on the Secretary, the Secretary shall
ensure that employees of the Food and Drug Administration do not deviate from such
guidances without appropriate justification and supervisory concurrence. The Secretary shall
provide training to employees in how to develop and use guidance documents and shall
monitor the development and issuance of such documents.
(C) For guidance documents that set forth initial interpretations of a statute or regulation,
changes in interpretation or policy that are of more than a minor nature, complex scientific
issues, or highly controversial issues, the Secretary shall ensure public participation prior to
implementation of guidance documents, unless the Secretary determines that such prior public
participation is not feasible or appropriate. In such cases, the Secretary shall provide for public
comment upon implementation and take such comment into account.
(D) For guidance documents that set forth existing practices or minor changes in policy, the
Secretary shall provide for public comment upon implementation.
(2) In developing guidance documents, the Secretary shall ensure uniform nomenclature for
such documents and uniform internal procedures for approval of such documents. The
Secretary shall ensure that guidance documents and revisions of such documents are properly
dated and indicate the nonbinding nature of the documents. The Secretary shall periodically
review all guidance documents and, where appropriate, revise such documents.
(3) The Secretary, acting through the Commissioner, shall maintain electronically and update
and publish periodically in the Federal Register a list of guidance documents. All such
documents shall be made available to the public.
(4) The Secretary shall ensure that an effective appeals mechanism is in place to address
complaints that the Food and Drug Administration is not developing and using guidance
documents in accordance with this subsection.
(5) Not later than July 1, 2000, the Secretary after evaluating the effectiveness of the Good
Guidance Practices document, published in the Federal Register at 62 Fed. Reg. 8961, shall
promulgate a regulation consistent with this subsection specifying the policies and procedures
of the Food and Drug Administration for the development, issuance, and use of guidance
documents.
EXAMINATIONS AND INVESTIGATIONS
SEC. 702. [21 U.S.C. 372] (a) (1)The Secretary is authorized to conduct examinations and
investigations for the purposes of this Act through officers and employees of the Department or
through any health, food, or drug officer or employee of any State, Territory, or political
subdivision thereof, duly commissioned by the Secretary as an officer of the Department.
(2)(A) In addition to the authority established in paragraph (1), the Secretary, pursuant to a
memorandum of understanding between the Secretary and the head of another Federal
department or agency, is authorized to conduct examinations and investigations for the
purposes of this Act through the officers and employees of such other department or agency,
subject to subparagraph (B). Such a memorandum shall include provisions to ensure
adequate training of such officers and employees to conduct the examinations and
investigations. The memorandum of understanding shall contain provisions regarding
reimbursement. Such provisions may, at the sole discretion of the head of the other
department or agency, require reimbursement, in whole or in part, from the Secretary for the
examinations or investigations performed under this section by the officers or employees of
the other department or agency.
(B) A memorandum of understanding under subparagraph (A) between the Secretary and
another Federal department or agency is effective only in the case of examinations or
inspections at facilities or other locations that are jointly regulated by the Secretary and such
department or agency.
(C) For any fiscal year in which the Secretary and the head of another Federal department or
agency carries out one or more examinations or inspections under a memorandum of
understanding under subparagraph (A), the Secretary and the head of such department or
agency shall with respect to their respective departments or agencies submit to the
committees of jurisdiction (authorizing and appropriating) in the House of Representatives and
the Senate a report that provides, for such year--
(i) the number of officers or employees that carried out one or more programs, projects, or
activities under such memorandum;
(ii) the number of additional articles that were inspected or examined as a result of such
memorandum; and
(iii) the number of additional examinations or investigations that were carried out pursuant to
such memorandum.
(3) In the case of food packed in the Commonwealth of Puerto Rico or a Territory the
Secretary shall attempt to make inspection of such food at the first point of entry within the
United States, when in his opinion and with due regard to the enforcement of all the provisions
of this Act, the facilities at his disposal will permit of such inspection.
(4) For the purposes of this subsection the term ‘‘ United States’’ means the States and the
District of Columbia.
(b) Where a sample of a food, drug, or cosmetic is collected for analysis under this Act the
Secretary shall, upon request, provide a part of such official sample for examination or
analysis by any person named on the label of the article, or the owner thereof, or his attorney
or agent; except that the Secretary is authorized, by regulations, to make such reasonable
exceptions from, and impose such reasonable terms and conditions relating to, the operation
of this subsection as he finds necessary for the proper administration of the provisions of this
Act.
(c) For purposes of enforcement of this Act, records of any department or independent
establishment in the executive branch of the Government shall be open to inspection by any
official of the Department duly authorized by the Secretary to make such inspection.
(d) The Secretary is authorized and directed, upon request from the Under Secretary of
Commerce for Intellectual Property and Director of the United States Patent and Trademark
Office, to furnish full and complete information with respect to such questions relating to drugs
as the Director may submit concerning any patent application. The Secretary is further
authorized, upon receipt of any such request, to conduct or cause to be conducted, such
research as may be required.
(e) Any officer or employee of the Department designated by the Secretary to conduct
examinations, investigations, or inspections under this Act relating to counterfeit drugs may,
when so authorized by the Secretary—
(1) carry firearms;
(2) execute and serve search warrants and arrest warrants;
(3) execute seizure by process issued pursuant to libel under section 304;
(4) make arrests without warrant for offenses under this Act with respect to such drugs if the
offense is committed in his presence or, in the case of a felony, if he has probable cause to
believe that the person so arrested has committed, or is committing, such offense; and
(5) make, prior to the institution of libel proceedings under section 304(a)(2), seizures of drugs
or containers or of equipment, punches, dies, plates, stones, labeling, or other things, if they
are, or he has reasonable grounds to believe that they are, subject to seizure and
condemnation under such section 304(a)(2). In the event of seizure pursuant to this paragraph
(5) 2 , libel proceedings under section 304(a)(2) shall be instituted promptly and the property
seized be placed under the jurisdiction of the court.
RECORDS OF INTERSTATE SHIPMENT
SEC. 703. [21 U.S.C. 373] Records. (a) In general.For the purpose of enforcing the provisions
of this Act, carriers engaged in interstate commerce, and persons receiving food, drugs,
devices, or cosmetics in interstate commerce or holding such articles so received, shall, upon
the request of an officer or employee duly designated by the Secretary, permit such officer or
employee, at reasonable times, to have access to and to copy all records showing the
movement in interstate commerce of any food, drug, device, or cosmetic, or the holding
thereof during or after such movement, and the quantity, shipper, and consignee thereof; and it
shall be unlawful for any such carrier or person to fail to permit such access to and copying of
any such record so requested when such request is accompanied by a statement in writing
specifying the nature or kind of food, drug, device, or cosmetic to which such request relates,
except that evidence obtained under this section, or any evidence which is directly or indirectly
derived from such evidence, shall not be used in a criminal prosecution of the person from
whom obtained, and except that carriers shall not be subject to the other provisions of this Act
by reason of their receipt, carriage, holding, or delivery of food, drugs, devices, or cosmetics in
the usual course of business as carriers.
(b) Food transportation records. A shipper, carrier by motor vehicle or rail vehicle, receiver, or
other person subject to section 416 shall, on request of an officer or employee designated by
the Secretary, permit the officer or employee, at reasonable times, to have access to and to
copy all records that the Secretary requires to be kept under section 416(c)(1)(E).
FACTORY INSPECTION
SEC. 704. [21 U.S.C. 374] (a)(1) For purposes of enforcement of this Act, officers or
employees duly designated by the Secretary, upon presenting appropriate credentials and a
written notice to the owner, operator, or agent in charge, are authorized (A) to enter, at
reasonable times, any factory, warehouse, or establishment in which food, drugs, devices, or
cosmetics are manufactured, processed, packed, or held, for introduction into interstate
commerce or after such introduction, or to enter any vehicle, being used to transport or hold
such food, drugs, devices, or cosmetics in interstate commerce; and (B) to inspect, at
reasonable times and within reasonable limits and in a reasonable manner, such factory,
warehouse, establishment, or vehicle and all pertinent equipment, finished and unfinished
materials, containers, and labeling therein. In the case of any person (excluding farms and
restaurants) who manufactures, processes, packs, transports, distributes, holds, or imports
foods, the inspection shall extend to all records and other information described in section 414
when the Secretary has a reasonable belief that an article of food is adulterated and presents
a threat of serious adverse health consequences or death to humans or animals, subject to the
limitations established in section 414(d). In the case of any factory, warehouse, establishment,
or consulting laboratory in which prescription drugs, nonprescription drugs intended for human
use, or restricted devices are manufactured, processed, packed, or held, inspection shall
extend to all things therein (including records, files, papers, processes, controls, and facilities)
bearing on whether prescription drugs, nonprescription drugs intended for human use, or
restricted devices which are adulterated or misbranded within the meaning of this Act, or which
may not be manufactured, introduced into interstate commerce, or sold, or offered for sale by
reason of any provision of this Act, have been or are being manufactured, processed, packed,
transported, or held in any such place, or otherwise bearing on violation of this Act. No
inspection authorized by the preceding sentence or by paragraph (3) shall extend to financial
data, sales data other than shipment data, pricing data, personnel data (other than data as to
qualifications of technical and professional personnel performing functions subject to this Act),
and research data (other than data relating to new drugs, antibiotic drugs, and devices and
subject to reporting and inspection under regulations lawfully issued pursuant to section 505(i)
or (k) 3 section 519, or 520(g), and data relating to other drugs or devices which in the case of
a new drug would be subject to reporting or inspection under lawful regulations issued
pursuant to section 505(j)). A separate notice shall be given for each such inspection, but a
notice shall not be required for each entry made during the period covered by the inspection.
Each such inspection shall be commenced and completed with reasonable promptness.
(2) The provisions of the third sentence of paragraph (1) shall not apply to—
(A) pharmacies which maintain establishments in conformance with any applicable local laws
regulating the practice of pharmacy and medicine and which are regularly engaged in
dispensing prescription drugs or devices, upon prescriptions of practitioners licensed to
administer such drugs or devices to patients under the care of such practitioners in the course
of their professional practice, and which do not, either through a subsidiary or otherwise,
manufacture, prepare, propagate, compound, or process drugs or devices for sale other than
in the regular course of their business of dispensing or selling drugs or devices at retail;
(B) practitioners licensed by law to prescribe or administer drugs, or prescribe or use devices,
as the case may be, and who manufacture, prepare, propagate, compound, or process drugs,
or manufacture or process devices solely for use in the course of their professional practice;
(C) persons who manufacture, prepare, propagate, compound, or process drugs, or
manufacture or process devices solely for use in research, teaching, or chemical analysis and
not for sale;
(D) such other classes of persons as the Secretary may by regulation exempt from the
application of this section upon a finding that inspection as applied to such classes of persons
in accordance with this section is not necessary for the protection of the public health.
(3) An officer or employee making an inspection under paragraph (1) for purposes of enforcing
the requirements of section 412 applicable to infant formulas shall be permitted, at all
reasonable times, to have access to and to copy and verify any records—
(A) bearing on whether the infant formula manufactured or held in the facility inspected meets
the requirements of section 412, or
(B) required to be maintained under section 412.
(b) Upon completion of any such inspection of a factory, warehouse, consulting laboratory, or
other establishment, and prior to leaving the premises, the officer or employee making the
inspection shall give to the owner, operator, or agent in charge a report in writing setting forth
any conditions or practices observed by him which, in his judgment, indicate that any food,
drug, device, or cosmetic in such establishment (1) consists in whole or in part of any filthy,
putrid, or decomposed substance, or (2) has been prepared, packed, or held under insanitary
conditions whereby it may have become contaminated with filth, or whereby it may have been
rendered injurious to health. A copy of such report shall be sent promptly to the Secretary.
(c) If the officer or employee making any such inspection of a factory, warehouse, or other
establishment has obtained any sample in the course of the inspection, upon completion of the
inspection and prior to leaving the premises he shall give to the owner, operator, or agent in
charge a receipt describing the samples obtained.
(d) Whenever in the course of any such inspection of a factory or other establishment where
food is manufactured, processed, or packed, the officer or employee making the inspection
obtains a sample of any such food, and an analysis is made of such sample for the purpose of
ascertaining whether such food consists in whole or in part of any filthy, putrid, or decomposed
substance, or is otherwise unfit for food, a copy of the results of such analysis shall be
furnished promptly to the owner, operator, or agent in charge.
(e) Every person required under section 519 or 520(g) to maintain records and every person
who is in charge or custody of such records shall, upon request of an officer or employee
designated by the Secretary, permit such officer or employee at all reasonable times to have
access to, and to copy and verify, such records.
(f)(1) An accredited person described in paragraph (3) shall maintain records documenting the
training qualifications of the person and the employees of the person, the procedures used by
the person for handling confidential information, the compensation arrangements made by the
person, and the procedures used by the person to identify and avoid conflicts of interest. Upon
the request of an officer or employee designated by the Secretary, the person shall permit the
officer or employee, at all reasonable times, to have access to, to copy, and to verify, the
records.
(2) Within 15 days after the receipt of a written request from the Secretary an accredited
person described in paragraph (3) for copies of records described in paragraph (1), the person
shall produce the copies of the records at the place designated by the Secretary.
(3) For purposes of paragraphs (1) and (2), an accredited person described in this paragraph
is a person who—
(A) is accredited under subsection (g); or
(B) is accredited under section 523.
(g)(1) Not later than one year after the date of the enactment of this subsection 4 , the
Secretary shall, subject to the provisions of this subsection, accredit persons for the purpose of
conducting inspections of establishments that manufacture, prepare, propagate, compound, or
process class II or class III devices, which inspections are required under section 510(h) or are
inspections of such establishments required to register pursuant to section 510(i).
(2) Not later than 180 days after the date of enactment of this subsection, the Secretary shall
publish in the Federal Register criteria to accredit or deny accreditation to persons who
request to perform the duties specified in paragraph (1). Thereafter, the Secretary shall inform
those requesting accreditation, within 60 days after the receipt of such request, whether the
request for accreditation is adequate for review, and the Secretary shall promptly act on the
request for accreditation. Any resulting accreditation shall state that such person is accredited
to conduct inspections at device establishments identified in paragraph (1). The accreditation
of such person shall specify the particular activities under this subsection for which such
person is accredited. In the first year following the publication in the Federal Register of criteria
to accredit or deny accreditation to persons who request to perform the duties specified in
paragraph (1), the Secretary shall accredit no more than 15 persons who request to perform
duties specified in paragraph (1).
(3) An accredited person shall, at a minimum, meet the following requirements:
(A) Such person may not be an employee of the Federal Government.
(B) Such person shall be an independent organization which is not owned or controlled by a
manufacturer, supplier, or vendor of articles regulated under this Act and which has no
organizational, material, or financial affiliation (including a consultative affiliation) with such a
manufacturer, supplier, or vendor.
(C) Such person shall be a legally constituted entity permitted to conduct the activities for
which it seeks accreditation.
(D) Such person shall not engage in the design, manufacture, promotion, or sale of articles
regulated under this Act.
(E) The operations of such person shall be in accordance with generally accepted professional
and ethical business practices, and such person shall agree in writing that at a minimum the
person will--
(i) certify that reported information accurately reflects data reviewed, inspection observations
made, other matters that relate to or may influence compliance with this Act, and
recommendations made during an inspection or at an inspection's closing meeting;
(ii) limit work to that for which competence and capacity are available;
(iii) treat information received, records, reports, and recommendations as confidential
commercial or financial information or trade secret information, except such information may
be made available to the Secretary;
(iv) promptly respond and attempt to resolve complaints regarding its activities for which it is
accredited; and
(v) protect against the use, in carrying out paragraph (1), of any officer or employee of the
accredited person who has a financial conflict of interest regarding any product regulated
under this Act, and annually make available to the public disclosures of the extent to which the
accredited person, and the officers and employees of the person, have maintained compliance
with requirements under this clause relating to financial conflicts of interest.
(4) The Secretary shall publish on the Internet site of the Food and Drug Administration a list of
persons who are accredited under paragraph (2). Such list shall be updated to ensure that the
identity of each accredited person, and the particular activities for which the person is
accredited, is known to the public. The updating of such list shall be no later than one month
after the accreditation of a person under this subsection or the suspension or withdrawal of
accreditation, or the modification of the particular activities for which the person is accredited.
(5)(A) To ensure that persons accredited under this subsection continue to meet the standards
of accreditation, the Secretary shall (i) audit the performance of such persons on a periodic
basis through the review of inspection reports and inspections by persons designated by the
Secretary to evaluate the compliance status of a device establishment and the performance of
accredited persons, and (ii) take such additional measures as the Secretary determines to be
appropriate.
(B) The Secretary may withdraw accreditation of any person accredited under paragraph (2),
after providing notice and an opportunity for an informal hearing, when such person is
substantially not in compliance with the standards of accreditation, poses a threat to public
health, fails to act in a manner that is consistent with the purposes of this subsection, or where
the Secretary determines that there is a financial conflict of interest in the relationship between
the accredited person and the owner or operator of a device establishment that the accredited
person has inspected under this subsection. The Secretary may suspend the accreditation of
such person during the pendency of the process under the preceding sentence.
(6)(A) Subject to subparagraphs (B) and (C), a device establishment is eligible for inspections
by persons accredited under paragraph (2) if the following conditions are met:
(i) The Secretary classified the results of the most recent inspection described in paragraph (1)
as "no action indicated" or "voluntary action indicated".
(ii) With respect inspections to be conducted by an accredited person--
(I) the owner or operator of the establishment submits to the Secretary a notice requesting
clearance to use an accredited person to conduct the inspection, and the Secretary provides
such clearance; and
(II) such notice identifies the accredited person whom the establishment has selected to
conduct the inspection, and the Secretary agrees to the selected accredited person.
(iii) With respect to the devices that are manufactured, prepared, propagated, compounded, or
processed by the establishment, at least one of such devices is marketed in the United States,
and 1 or both of the following additional conditions are met:
(I) At least one of such devices is marketed, or is intended to be marketed, or is intended to be
marketed, in one or more foreign countries, one of which countries certifies, accredits, or
otherwise recognizes the person (accredited under paragraph (2) and identified under clause
(ii)(I)) as a person authorized to conduct such inspections of device establishments.
(II) The owner or operator of the establishment submits to the Secretary a statement that the
law of a country in which such a device is marketed, or is intended to be marketed, recognizes
an inspection of the establishment by the Secretary or by a person accredited under paragraph
(2), and not later than 30 days after receiving such statement, the Secretary informs the owner
or operator of the establishment that the owner or operator may submit a notice requesting
clearance under clause (ii).
(iv)(I) In the case of an inspection to be conducted pursuant to section 510(h), persons
accredited under paragraph (2) did not conduct inspections of the establishment during the
previous 4 years, except that the establishment may petition the Secretary for a waiver of such
condition. Such a waiver may be granted only if the petition states a commercial reason for the
waiver; the Secretary determines that the public health would be served by granting the waiver;
and the Secretary has conducted an inspection of the establishment during the four-year
period preceding the date on which the notice under clause (ii) is submitted to the Secretary.
Such a waiver is deemed to be granted only if the Secretary has not determined that the public
health would not be served by granting the waiver; and the owner or operator of the device
establishment has requested in writing, not later than 18 months following the most recent
inspection of such establishment by a person accredited under paragraph (2), that the
Secretary inspect the establishment and the Secretary has not conducted an inspection within
30 months after the most recent inspection. With respect to such a waiver that is granted or
deemed to be granted, no additional such waiver may be granted or deemed to be granted
until after the Secretary has conducted an inspection of the establishment.
(II) In the case of an inspection to be conducted of a device establishment required to register
pursuant to section 510(i), the Secretary periodically conducts inspections of the
establishment.
(B)(i) The Secretary shall respond to a notice under subparagraph (A) from a device
establishment not later than 30 days after the Secretary receives the notice. Through such
response, the Secretary shall (I) provide clearance under such subparagraph, and agree to the
selection of an accredited person, or (II) make a request under clause (ii). If the Secretary fails
to respond to the notice within such 30-day period, the establishment is deemed to have such
clearance, and to have the agreement of the Secretary for such selection.
(ii) The request referred to in clause (i)(II) is—
(I) a request to the device establishment involved to submit to the Secretary compliance data
in accordance with clause (iii); or
(II) a request to the establishment, or to the accredited person identified in the notice under
subparagraph (A), for information concerning the relationship between the establishment and
such accredited person, including information about the number of inspections of the
establishment, or other establishments owned or operated by the owner or operator of the
establishment, that have been conducted by the accredited person. The Secretary may make
both such requests.
(iii) The compliance data to be submitted by a device establishment under clause (ii) are data
describing whether the quality controls of the establishment have been sufficient for ensuring
consistent compliance with current good manufacturing practice within the meaning of section
501(h) and with other applicable provisions of this Act. Such data shall include complete
reports of inspectional findings regarding good manufacturing practice or other quality control
audits that, during the preceding two-year period, were conducted at the establishment by
persons other than the owner or operator of the establishment, together with all other relevant
compliance data the Secretary deems necessary. Data under the preceding sentence shall
demonstrate to the Secretary whether the establishment has facilitated consistent compliance
by promptly correcting any compliance problems identified in such inspections.
(iv) (I) Not later than 60 days after receiving compliance data under clause (iii) from a device
establishment, the Secretary shall provide or deny clearance under subparagraph (A). The
Secretary may deny clearance if the Secretary determines that the establishment has failed to
demonstrate consistent compliance for purposes of clause (iii). The Secretary shall provide to
the establishment a statement of such reasons for such determination. If the Secretary fails to
provide such statement to the establishment within such 60-day period, the establishment is
deemed to have such clearance.
(II) If, during the two-year period following clearance under subparagraph (A), the Secretary
determines that the device establishment is substantially not in compliance with this Act, the
Secretary may, after notice and a written response, notify the establishment that the eligibility
of the establishment for the inspections by accredited persons has been suspended.
(v)(I) A request to an accredited person under clause (ii)(II) may not seek any information that
is not required to be maintained by such person in records under subsection (f)(1). Not later
than 60 days after receiving the information sought by the request, the Secretary shall agree to,
or reject, the selection of such person by the device establishment involved. The Secretary
may reject the selection if the Secretary provides to the establishment a statement of the
reasons for such rejection. Reasons for the rejection may include that the establishment or the
accredited person, as the case may be, has failed to fully respond to the request, or that the
Secretary has concerns regarding the relationship between the establishment and such
accredited person. If within such 60-day period the Secretary fails to agree to or reject the
selection in accordance with this subclause, the Secretary is deemed to have agreed to the
selection.
(II) If the Secretary rejects the selection of an accredited person by a device establishment, the
establishment may make an additional selection of an accredited person by submitting to the
Secretary a notice that identifies the additional selection. Clauses (i) and (ii), and subclause (I)
of this clause, apply to the selection of an accredited person through a notice under the
preceding sentence in the same manner and to the same extent as such provisions apply to a
selection of an accredited person through a notice under subparagraph (A).
(vi) In the case of a device establishment that under clause (iv) is denied clearance under
subparagraph (A), or whose selection of an accredited person is rejected under clause (v), the
Secretary shall designate a person to review the findings of the Secretary under such clause if,
during the 30-day period beginning on the date on which the establishment receives the
findings, the establishment requests the review. The review shall commence not later than 30
days after the establishment requests the review, unless the Secretary and the establishment
otherwise agree.
(C)(i) In the case of a device establishment for which the Secretary classified the results of the
most recent inspection of the establishment by a person accredited under paragraph (2) as
`official action indicated', the establishment, if otherwise eligible under subparagraph (A), is
eligible for further inspections by persons accredited under such paragraph if (I) the Secretary
issues a written statement to the owner or operator of the establishment that the violations
leading to such classification have been resolved, and (II) the Secretary, either upon the
Secretary's own initiative or a petition of the owner or operator of the establishment, notifies
the establishment that it has clearance to use an accredited person for the inspections. The
Secretary shall respond to such petition within 30 days after the receipt of the petition.
(ii) If the Secretary denies a petition under clause (i), the device establishment involved may,
after the expiration of one year after such denial, again petition the Secretary for a
determination of eligibility for inspection by persons accredited by the Secretary under
paragraph (2). If the Secretary denies such petition, the Secretary shall provide the
establishment with such reasons for such denial within 60 days after the denial. If, as of the
expiration of 48 months after the receipt of the first petition, the establishment has not been
inspected by the Secretary, the establishment is eligible for further inspections by accredited
persons.
(7)(A) Persons accredited under paragraph (2) to conduct inspections shall record in writing
their inspection observations and shall present the observations to the device establishment's
designated representative and describe each observation. Additionally, such accredited
person shall prepare an inspection report (including for inspections classified as `no action
indicated') in a form and manner consistent with such reports prepared by employees and
officials designated by the Secretary to conduct inspections.
(B) At a minimum, an inspection report under subparagraph (A) shall identify the persons
responsible for good manufacturing practice compliance at the inspected device establishment,
the dates of the inspection, the scope of the inspection, and shall describe in detail each
observation identified by the accredited person, identify other matters that relate to or may
influence compliance with this Act, and describe any recommendations during the inspection
or at the inspection's closing meeting.
(C) An inspection report under subparagraph (A) shall be sent to the Secretary and to the
designated representative of the inspected device establishment at the same time, but under
no circumstances later than three weeks after the last day of the inspection. The report to the
Secretary shall be accompanied by all written inspection observations previously provided to
the designated representative of the establishment.
(D) Any statement or representation made by an employee or agent of a device establishment
to a person accredited under paragraph (2) to conduct inspections shall be subject to section
1001 of title 18, United States Code.
(E) If at any time during an inspection by an accredited person the accredited person discovers
a condition that could cause or contribute to an unreasonable risk to the public health, the
accredited person shall immediately notify the Secretary of the identification of the device
establishment subject to inspection and such condition.
(8) Compensation for an accredited person shall be determined by agreement between the
accredited person and the person who engages the services of the accredited person, and
shall be paid by the person who engages such services.
(9) Nothing in this subsection affects the authority of the Secretary to inspect any device
establishment pursuant to this Act.
(10)(A) For fiscal year 2005 and each subsequent fiscal year, no device establishment may be
inspected during the fiscal year involved by a person accredited under paragraph (2) if—
(i) of the amounts appropriated for salaries and expenses of the Food and Drug Administration
for the preceding fiscal year (referred to in this subparagraph as the `first prior fiscal year'), the
amount obligated by the Secretary for inspections of device establishments by the Secretary
was less than the adjusted base amount applicable to such first prior fiscal year; and
(ii) of the amounts appropriated for salaries and expenses of the Food and Drug Administration
for the fiscal year preceding the first prior fiscal year (referred to in this subparagraph as the
`second prior fiscal year'), the amount obligated by the Secretary for inspections of device
establishments by the Secretary was less than the adjusted base amount applicable to such
second prior fiscal year.
(B)(i) Subject to clause (ii), the Comptroller General of the United States shall determine the
amount that was obligated by the Secretary for fiscal year 2002 for compliance activities of the
Food and Drug Administration with respect to devices (referred to in this subparagraph as the
`compliance budget'), and of such amount, the amount that was obligated for inspections by
the Secretary of device establishments (referred to in this subparagraph as the `inspection
budget').
(ii) For purposes of determinations under clause (i), the Comptroller General shall not include
in the compliance budget or the inspection budget any amounts obligated for inspections of
device establishments conducted as part of the process of reviewing applications under
section 515.
(iii) Not later than March 31, 2003 , the Comptroller General shall complete the determinations
required in this subparagraph and submit to the Secretary and the Congress a report
describing the findings made through such determinations.
(C) For purposes of this paragraph:
(i) The term `base amount' means the inspection budget determined under subparagraph (B)
for fiscal year 2002.
(ii) The term `adjusted base amount', in the case of applicability to fiscal year 2003, means an
amount equal to the base amount increased by 5 percent.
(iii) The term `adjusted base amount', with respect to applicability to fiscal year 2004 or any
subsequent fiscal year, means the adjusted based amount 5 applicable to the preceding year
increased by 5 percent.
(11) The authority provided by this subsection terminates on October 1, 2012 .
(12) No later than four years after the enactment of this subsection the Comptroller General
shall report to the Committee on Energy and Commerce of the House of Representatives and
the Committee on Health, Education, Labor and Pensions of the Senate—
(A) the number of inspections conducted by accredited persons pursuant to this subsection
and the number of inspections conducted by Federal employees pursuant to section 510(h)
and of device establishments required to register under section 510(i);
(B) the number of persons who sought accreditation under this subsection, as well as the
number of persons who were accredited under this subsection;
(C) the reasons why persons who sought accreditation, but were denied accreditation, were
denied;
(D) the number of audits conducted by the Secretary of accredited persons, the quality of
inspections conducted by accredited persons, whether accredited persons are meeting their
obligations under this Act, and whether the number of audits conducted is sufficient to permit
these assessments;
(E) whether this subsection is achieving the goal of ensuring more information about device
establishment compliance is being presented to the Secretary, and whether that information is
of a quality consistent with information obtained by the Secretary pursuant to inspections
conducted by Federal employees;
(F) whether this subsection is advancing efforts to allow device establishments to rely upon
third-party inspections for purposes of compliance with the laws of foreign governments; and
(G) whether the Congress should continue, modify, or terminate the program under this
subsection.
(13) The Secretary shall include in the annual report required under section 903(g) the names
of all accredited persons and the particular activities under this subsection for which each such
person is accredited and the name of each accredited person whose accreditation has been
withdrawn during the year.
(14) Notwithstanding any provision of this subsection, this subsection does not have any legal
effect on any agreement described in section 803(b) between the Secretary and a foreign
country.
PUBLICITY
SEC. 705. [21 U.S.C. 375] (a) The Secretary shall cause to be published from time to time
reports summarizing all judgments, decrees, and court orders which have been rendered
under this Act, including the nature of the charge and the disposition thereof.
(b) The Secretary may also cause to be disseminated information regarding food, drugs,
devices, or cosmetics in situations involving, in the opinion of the Secretary, imminent danger
to health, or gross deception of the consumer. Nothing in this section shall be construed to
prohibit the Secretary from collecting, reporting, and illustrating the results of the investigations
of the Department.
SEAFOOD INSPECTION
SEC. 706. [21 U.S.C. 376] The Secretary, upon application of any packer of any seafood for
shipment or sale within the jurisdiction of this Act, may, at his discretion, designate inspectors
to examine and inspect such food and the production, packing, and labeling thereof. If on such
examination and inspection compliance is found with the provisions of this Act and regulations
promulgated thereunder, the applicant shall be authorized or required to mark the food as
provided by regulation to show such compliance. Services under this section shall be rendered
only upon payment by the applicant of fees fixed by regulation in such amounts as may be
necessary to provide, equip, and maintain an adequate and efficient inspection service.
Receipts from such fees shall be covered into the Treasury and shall be available to the
Secretary for expenditures incurred in carrying out the purposes of this section, including
expenditures for salaries of additional inspectors when necessary to supplement the number
of inspectors for whose salaries Congress has appropriated. The Secretary is hereby
authorized to promulgate regulations governing the sanitary and other conditions under which
the service herein provided shall be granted and maintained and for otherwise carrying out the
purposes of this section. Any person who forges, counterfeits, simulates, or falsely represents,
or without proper authority uses any mark, stamp, tag, label, or other identification devices
authorized or required by the provisions of this section or regulations thereunder, shall be
guilty of a misdemeanor, and shall on conviction thereof be subject to imprisonment for not
more than one year or a fine of not less than $1,000 nor more than $5,000 or both such
imprisonment and fine.
ADVERTISING OF CERTAIN FOODS
SEC. 707. [21 U.S.C. 378] (a)(1) Except as provided in subsection (c), before the Secretary
may initiate any action under chapter III—
(A) with respect to any food which the Secretary determines is misbranded under section
403(a)(2) because of its advertising, or
(B) with respect to a food’s advertising which the Secretary determines causes the food to be
so misbranded,
the Secretary shall, in accordance with paragraph (2), notify in writing the Federal Trade
Commission of the action the Secretary proposes to take respecting such food or advertising.
(2) The notice required by paragraph (1) shall—
(A) contain (i) a description of the action the Secretary proposes to take and of the advertising
which the Secretary has determined causes a food to be misbranded, (ii) a statement of the
reasons for the Secretary’s determination that such advertising has caused such food to be
misbranded, and
(B) be accompanied by the records, documents, and other written materials which the
Secretary determines supports his determination that such food is misbranded because of
such advertising.
(b)(1) If the Secretary notifies the Federal Trade Commission under subsection (a) of action
proposed to be taken under chapter III with respect to a food or food advertising and the
Commission notifies the Secretary in writing, within the 30-day period beginning on the date of
the receipt of such notice, that—
(A) it has initiated under the Federal Trade Commission Act an investigation of such
advertising to determine if it is prohibited by such Act or any order or rule under such Act,
(B) it has commenced (or intends to commence) a civil action under section 5, 13, or 19 with
respect to such advertising or the Attorney General has commenced (or intends to commence)
a civil action under section 5 with respect to such advertising,
(C) it has issued and served (or intends to issue and serve) a complaint under section 5(b) of
such Act respecting such advertising, or
(D) pursuant to section 16(b) of such Act it has made a certification to the Attorney General
respecting such advertising, the Secretary may not, except as provided by paragraph (2),
initiate the action described in the Secretary’s notice to the Federal Trade Commission.
(2) If, before the expiration of the 60-day period beginning on the date the Secretary receives a
notice described in paragraph (1) from the Federal Trade Commission in response to a notice
of the Secretary under subsection (a)—
(A) the Commission or the Attorney General does not commence a civil action described in
subparagraph (B) of paragraph (1) of this subsection respecting the advertising described in
the Secretary’s notice,
(B) the Commission does not issue and serve a complaint described in subparagraph (C) of
such paragraph respecting such advertising, or
(C) the Commission does not (as described in subparagraph (D) of such paragraph) make a
certification to the Attorney General respecting such advertising, or, if the Commission does
make such a certification to the Attorney General respecting such advertising, the Attorney
General, before the expiration of such period, does not cause appropriate criminal
proceedings to be brought against such advertising,
the Secretary may, after the expiration of such period, initiate the action described in the notice
to the Commission pursuant to subsection (a). The Commission shall promptly notify the
Secretary of the commencement by the Commission of such a civil action, the issuance and
service by it of such a complaint, or the causing by the Attorney General of criminal
proceedings to be brought against such advertising.
(c) The requirements of subsections (a) and (b) do not apply with respect to action under
chapter III with respect to any food or food advertising if the Secretary determines that such
action is required to eliminate an imminent hazard to health.
(d) For the purpose of avoiding unnecessary duplication, the Secretary shall coordinate any
action taken under chapter III because of advertising which the Secretary determines causes a
food to be misbranded with any action of the Federal Trade Commission under the Federal
Trade Commission Act with respect to such advertising.
CONFIDENTIAL INFORMATION
SEC. 708. [21 U.S.C. 379] The Secretary may provide any information which is exempt from
disclosure pursuant to subsection (a) of section 552 of title 5, United States Code, by reason of
subsection (b)(4) of such section to a person other than an officer or employee of the
Department if the Secretary determines such other person requires the information in
connection with an activity which is undertaken under contract with the Secretary, which
relates to the administration of this Act, and with respect to which the Secretary (or an officer
or employee of the Department) is not prohibited from using such information. The Secretary
shall require as a condition to the provision of information under this section that the person
receiving it take such security precautions respecting the information as the Secretary may by
regulation prescribe.
PRESUMPTION
SEC. 709. [21 U.S.C. 379a] In any action to enforce the requirements of this Act respecting a
device, food, drug, or cosmetic the connection with interstate commerce required for
jurisdiction in such action shall be presumed to exist.
SEC. 710. [21 U.S.C. 379b] CONSOLIDATED ADMINISTRATIVE AND LABORATORY
FACILITY.
(a) AUTHORITY.—The Secretary, in consultation with the Administrator of the General
Services Administration, shall enter into contracts for the design, construction, and operation
of a consolidated Food and Drug Administration administrative and laboratory facility.
(b) AWARDING OF CONTRACT.—The Secretary shall solicit contract proposals under
subsection (a) from interested parties. In awarding contracts under such subsection, the
Secretary shall review such proposals and give priority to those alternatives that are the most
cost effective for the Federal Government and that allow for the use of donated land, federally
owned property, or lease-purchase arrangements. A contract under this subsection shall not
be entered into unless such contract results in a net cost savings to the Federal Government
over the duration of the contract, as compared to the Government purchase price including
borrowing by the Secretary of the Treasury.
(c) DONATIONS.—In carrying out this section, the Secretary shall have the power, in
connection with real property, buildings, and facilities, to accept on behalf of the Food and
Drug Administration gifts or donations of services or property, real or personal, as the
Secretary determines to be necessary.
(d) AUTHORIZATION OF APPROPRIATIONS.—There are authorized to be appropriated to
carry out this section $100,000,000 for fiscal year 1991, and such sums as may be necessary
for each of the subsequent fiscal years, to remain available until expended.
SEC. 711. [21 U.S.C. 379d] AUTOMATION OF FOOD AND DRUG ADMINISTRATION.
(a) IN GENERAL.—The Secretary, acting through the Commissioner of Food and Drugs, shall
automate appropriate activities of the Food and Drug Administration to ensure timely review of
activities regulated under this Act.
(b) AUTHORIZATION OF APPROPRIATIONS.—There are authorized to be appropriated
each fiscal year such sums as are necessary to carry out this section.
Footnotes: Chapter VII, Subchapter A
1. The probable intent of the Congress is that the reference to maple sirup be struck. Section
3(b) of Public Law 103–396 attempted to amend subsection (e)(1) by striking "or maple syrup
(regulated under section 168.140 of title 21, Code of Federal Regulations).". The amendment
cannot be executed because the amendatory instructions referred to ‘‘maple syrup’’ rather
than "maple sirup".
2. So in law. Probably should be "this paragraph".
3. So in law. A comma probably should appear after "section 505(i) or (k)". See the
amendment made by section 125(b)(2)(L) of Public Law 105–115 (111 Stat. 2326).
4. Subsection (g) was added by section 201 of Public Law 107–250 (116 Stat. 1602), which
was enacted October 26, 2002.
5. So in law. See section 201(a) of Public Law 107–250 (116 Stat. 1602, 1608). Probably
should be "adjusted base amount".
CHAPTER VII—GENERAL AUTHORITY SUBCHAPTER B--COLORS
LISTING AND CERTIFICATION OF COLOR ADDITIVES FOR FOODS, DRUGS, AND
COSMETICS
When Color Additives Deemed Unsafe
SEC. 721. 1 [21 U.S.C. 379e] (a) A color additive shall, with respect to any particular use (for
which it is being used or intended to be used or is represented as suitable) in or on food or
drugs or devices or cosmetics be deemed unsafe for the purposes of the application of section
402(c), section 501(a)(4), or section 601(e), as the case may be unless—
(1)(A) there is in effect, and such additive and such use are in conformity with, a regulation
issued under subsection (b) of this section listing such additive for such use, including any
provision of such regulation prescribing the conditions under which such additive may be
safely used, and (B) such additive either (i) is from a batch certified, in accordance with
regulations issued pursuant to subsection (c), for such use, or (ii) has, with respect to such use,
been exempted by the Secretary from the requirement of certification; or
(2) such additive and such use thereof conform to the terms of an exemption which is in effect
pursuant to subsection (f) of this section.
While there are in effect regulations under subsections (b) and (c) of this section relating to a
color additive or an exemption pursuant to subsection (f) with respect to such additive, an
article shall not, by reason of bearing or containing such additive in all respects in accordance
with such regulations or such exemption, be considered adulterated within the meaning of
clause (1) of section 402(a) if such article is a food, or within the meaning of section 601(a) if
such article is a cosmetic other than a hair dye (as defined in the last sentence of section
601(a)). A color additive for use in or on a device shall be subject to this section only if the
color additive comes in direct contact with the body of man or other animals for a significant
period of time. The Secretary may by regulation designate the uses of color additives in or on
devices which are subject to this section.
Listing of Colors
(b)(1) The Secretary shall, by regulation, provide for separately listing color additives for use in
or on food, color additives for use in or on drugs or devices, and color additives for use in or on
cosmetics, if and to the extent that such additives are suitable and safe for any such use when
employed in accordance with such regulations.
(2)(A) Such regulations may list any color additive for use generally in or on food, or in or on
drugs or devices, or in or on cosmetics, if the Secretary finds that such additive is suitable and
may safely be employed for such general use.
(B) If the data before the Secretary do not establish that the additive satisfies the requirements
for listing such additive on the applicable list pursuant to subparagraph (A) of this paragraph,
or if the proposal is for listing such additive for a more limited use or uses, such regulations
may list such additive only for any more limited use or uses for which it is suitable and may
safely be employed.
(3) Such regulations shall, to the extent deemed necessary by the Secretary to assure the
safety of the use or uses for which a particular color additive is listed, prescribe the conditions
under which such additive may be safely employed for such use or uses (including, but not
limited to, specifications, hereafter in this section referred to as tolerance limitations, as to the
maximum quantity or quantities which may be used or permitted to remain in or on the article
or articles in or on which it is used; specifications as to the manner in which such additive may
be added to or used in or on such article or articles; and directions or other labeling or
packaging requirements for such additive).
(4) The Secretary shall not list a color additive under this section for a proposed use unless the
data before him establish that such use, under the conditions of use specified in the
regulations, will be safe: Provided, however, That a color additive shall be deemed to be
suitable and safe for the purpose of listing under this subsection for use generally in or on food,
while there is in effect a published finding of the Secretary declaring such substance exempt
from the term ‘‘food additive’’ because of its being generally recognized by qualified experts as
safe for its intended use, as provided in section 201(s).
(5)(A) In determining, for the purposes of this section, whether a proposed use of a color
additive is safe, the Secretary shall consider, among other relevant factors—
(i) the probable consumption of, or other relevant exposure from, the additive and of any
substance formed in or on food, drugs or devices, or cosmetics because of the use of the
additive;
(ii) the cumulative effect, if any, of such additive in the diet of man or animals, taking into
account the same or any chemically or pharmacologically related substance or substances in
such diet;
(iii) safety factors which, in the opinion of experts qualified by scientific training and experience
to evaluate the safety of color additives for the use or uses for which the additive is proposed
to be listed, are generally recognized as appropriate for the use of animal experimentation
data; and
(iv) the availability of any needed practicable methods of analysis for determining the identity
and quantity of (I) the pure dye and all intermediates and other impurities contained in such
color additive, (II) such additive in or on any article of food, drug or devices, or cosmetic, and
(III) any substance formed in or on such article because of the use of such additive.
(B) A color additive (i) shall be deemed unsafe, and shall not be listed, for any use which will or
may result in ingestion of all or part of such additive, if the additive is found by the Secretary to
induce cancer when ingested by man or animal, or if it is found by the Secretary, after tests
which are appropriate for the evaluation of the safety of additives for use in food, to induce
cancer in man or animal, and (ii) shall be deemed unsafe, and shall not be listed, for any use
which will not result in ingestion of any part of such additive, if, after tests which are
appropriate for the evaluation of the safety of additives for such use, or after other relevant
exposure of man or animal to such additive, it is found by the Secretary to induce cancer in
man or animal: Provided, That clause (i) of this subparagraph (B) shall not apply with respect
to the use of a color additive as an ingredient of feed for animals which are raised for food
production, if the Secretary finds that, under the conditions of use and feeding specified in
proposed labeling and reasonably certain to be followed in practice, such additive will not
adversely affect the animals for which such feed is intended, and that no residue of the
additive will be found (by methods of examination prescribed or approved by the Secretary by
regulations, which regulations shall not be subject to subsection (d)) in any edible portion of
such animals after slaughter or in any food yielded by or derived from the living animal.
(C)(i) In any proceeding for the issuance, amendment, or repeal of a regulation listing a color
additive, whether commenced by a proposal of the Secretary on his own initiative or by a
proposal contained in a petition, the petitioner, or any other person who will be adversely
affected by such proposal or by the Secretary’s order issued in accordance with paragraph (1)
of section 701(e) if placed in effect, may request, within the time specified in this subparagraph,
that the petition or order thereon, or the Secretary’s proposal, be referred to an advisory
committee for a report and recommendations with respect to any matter arising under
subparagraph (B) of this paragraph, which is involved in such proposal or order and which
requires the exercise of scientific judgment. Upon such request, or if the Secretary within such
time deems such a referral necessary, the Secretary shall forthwith appoint an advisory
committee under subparagraph (D) of this paragraph and shall refer to it, together with all the
data before him, such matter arising under subparagraph (B) for study thereof and for a report
and recommendations on such matter. A person who has filed a petition or who has requested
the referral of a matter to an advisory committee pursuant to this subparagraph (C) 2 , as well
as representatives of the Department, shall have the right to consult with such advisory
committee in connection with the matter referred to it. The request for referral under this
subparagraph, or the Secretary’s referral on his own initiative, may be made at any time before,
or within thirty days after, publication of an order of the Secretary acting upon the petition or
proposal.
(ii) Within sixty days after the date of such referral, or within an additional thirty days if the
committee deems such additional time necessary, the committee shall, after independent
study of the data furnished to it by the Secretary and other data before it, certify to the
Secretary a report and recommendations, together with all underlying data and a statement of
the reasons or basis for the recommendations. A copy of the foregoing shall be promptly
supplied by the Secretary to any person who has filed a petition, or who has requested such
referral to the advisory committee. Within thirty days after such certification, and after giving
due consideration to all data then before him, including such report, recommendation,
underlying data, and statement, and to any prior order issued by him in connection with such
matter, the Secretary shall by order confirm or modify any order therefore issued or, if no such
prior order has been issued, shall by order act upon the petition or other proposal.
(iii) Where—
(I) by reason of subparagraph (B) of this paragraph, the Secretary has initiated a proposal to
remove from listing a color additive previously listed pursuant to this section; and
(II) a request has been made for referral of such proposal to an advisory committee; the
Secretary may not act by order on such proposal until the advisory committee has made a
report and recommendations to him under clause (ii) of this subparagraph and he has
considered such recommendations, unless the Secretary finds that emergency conditions
exist necessitating the issuance of an order notwithstanding this clause.
(D) The advisory committee referred to in subparagraph (C) of this paragraph shall be
composed of experts selected by the National Academy of Sciences, qualified in the subject
matter referred to the committee and of adequately diversified professional background,
except that in the event of the inability or refusal of the National Academy of Sciences to act,
the Secretary shall select the members of the committee. The size of the committee shall be
determined by the Secretary. Members of any advisory committee established under this Act,
while attending conferences or meetings of their committees or otherwise serving at the
request of the Secretary, shall be entitled to receive compensation at rates to be fixed by the
Secretary but at rates not exceeding the daily equivalent of the rate specified at the time of
such service for grade GS–18 of the General Schedule 3 , including travel time; and while
away from their homes or regular places of business they may be allowed travel expenses,
including per diem in lieu of subsistence, as authorized by section 5703 of title 5 of the United
States Code for persons in the Government service employed intermittently. The members
shall not be subject to any other provisions of law regarding the appointment and
compensation of employees of the United States. The Secretary shall furnish the committee
with adequate clerical and other assistance, and shall by rules and regulations prescribe the
procedure to be followed by the committee.
(6) The Secretary shall not list a color additive under this subsection for a proposed use if the
data before him show that such proposed use would promote deception of the consumer in
violation of this Act or would otherwise result in misbranding or adulteration within the meaning
of this Act.
(7) If, in the judgment of the Secretary, a tolerance limitation is required in order to assure that
a proposed use of a color additive will be safe, the Secretary—
(A) shall not list the additive for such use if he finds that the data before him do not establish
that such additive, if used within a safe tolerance limitation, would achieve the intended
physical or other technical effect; and
(B) shall not fix such tolerance limitation at a level higher than he finds to be reasonably
required to accomplish the intended physical or other technical effect.
(8) If, having regard to the aggregate quantity of color additive likely to be consumed in the diet
or to be applied to the human body, the Secretary finds that the data before him fail to show
that it would be safe and otherwise permissible to list a color additive (or pharmacologically
related color additives) of all uses proposed therefor and at the levels of concentration
proposed, the Secretary shall, in determining for which use or uses such additive (or such
related additives) shall be or remain listed, or how the aggregate allowable safe tolerance for
such additive or additives shall be allocated by him among the uses under consideration, take
into account, among other relevant factors (and subject to the paramount criterion of safety),
(A) the relative marketability of the articles involved as affected by the proposed uses of the
color additive (or of such related additives) in or on such articles, and the relative dependence
of the industries concerned on such uses; (B) the relative aggregate amounts of such color
additive which he estimates would be consumed in the diet or applied to the human body by
reason of the various uses and levels of concentration proposed; and (C) the availability, if any,
of other color additives suitable and safe for one or more of the uses proposed.
Certification of Colors
(c) The Secretary shall further, by regulation, provide (1) for the certification, with safe diluents
or without diluents, of batches of color additives listed pursuant to subsection (b) and
conforming to the requirements for such additives established by regulations under such
subsection and this subsection, and (2) for exemption from the requirement of certification in
the case of any such additive, or any listing or use thereof, for which he finds such requirement
not to be necessary in the interest of the protection of the public health: Provided, That, with
respect to any use in or on food for which a listed color additive is deemed to be safe by
reason of the proviso to paragraph (4) of subsection (b), the requirement of certification shall
be deemed not to be necessary in the interest of public health protection.
Procedure for Issuance, Amendment, or Repeal of Regulations
(d) The provisions of section 701 (e), (f), and (g) of this Act shall, subject to the provisions of
subparagraph (C) of subsection (b)(5) of this section, apply to and in all respects govern
proceedings for the issuance, amendment, or repeal of regulations under subsection (b) or (c)
of this section (including judicial review of the Secretary’s action in such proceedings) and the
admissibility of transcripts of the record of such proceedings in other proceedings, except
that—
(1) if the proceeding is commenced by the filing of a petition, notice of the proposal made by
the petition shall be published in general terms by the Secretary within thirty days after such
filing, and the Secretary’s order (required by paragraph (1) of section 701(e)) acting upon such
proposal shall, in the absence of prior referral (or request for referral) to an advisory committee,
be issued within ninety days after the date of such filing, except that the Secretary may (prior
to such ninetieth day) by written notice to the petitioner, extend such ninety-day period to such
time (not more than one hundred and eighty days after the date of filing of the petition) as the
Secretary deems necessary to enable him to study and investigate the petition;
(2) any report, recommendations, underlying data, and reasons certified to the Secretary by an
advisory committee appointed pursuant to subparagraph (D) of subsection (b)(5) of this
section, shall be made a part of the record of any hearing if relevant and material, subject to
the provisions of section 7(c) of the Administrative Procedure Act (5 U.S.C., sec. 1006(c)) 4 .
The advisory committee shall designate a member to appear and testify at any such hearing
with respect to the report and recommendations of such committee upon request of the
Secretary, the petitioner, or the officer conducting the hearing, but this shall not preclude any
other member of the advisory committee from appearing and testifying at such hearing;
(3) the Secretary’s order after public hearing (acting upon objections filed to an order made
prior to hearings) shall be subject to the requirements of section 409(f)(2); and
(4) the scope of judicial review of such order shall be in accordance with the fourth sentence of
paragraph (2), and with the provisions of paragraph (3), of section 409(g).
Fees
(e) The admitting to listing and certification of color additives, in accordance with regulations
prescribed under this Act, shall be performed only upon payment of such fees, which shall be
specified in such regulations, as may be necessary to provide, maintain, and equip an
adequate service for such purposes.
Exemptions
(f) The Secretary shall by regulations (issued without regard to subsection (d)) provide for
exempting from the requirements of this section any color additive or any specific type of use
thereof, and any article of food, drug or device, or cosmetic bearing or containing such additive,
intended solely for investigational use by qualified experts when in his opinion such exemption
is consistent with the public health.
NOTE.—Section 201 of the Labor-Federal Security Appropriation Act, 1944 (21 U.S.C. 377),
provides that the Secretary in carrying into effect this Act ‘‘is authorized to cooperate with
associations and scientific societies in the revision of the United States Pharmacopeia and in
the development of methods of analysis and mechanical and physical tests necessary to carry
out the work of the Food and Drug Administration.
Footnotes: Chapter VII, Subchapter B
1. See the revolving fund provision in the appendix.
2. So in law. Probably should be "this subparagraph".
3. The General Schedule under section 5332 of title 5, United States Code, no longer includes
the grade GS-18. The grades are GS-1 through GS-15.
4. Section 7(c) of the Administrative Procedure Act has been superseded by section 556(d) of
title 5, United States Code. See Public Law 89-554.
CHAPTER VII GENERAL AUTHORITY SUBCHAPTER C--FEES
PART 1 FREEDOM OF INFORMATION FEES
SEC. 731. [ 21 U.S.C. 379f] RECOVERY AND RETENTION OF FEES FOR FREEDOM OF
INFORMATION REQUESTS.
(a) IN GENERAL. The Secretary, acting through the Commissioner of Food and Drugs, may
(1) set and charge fees, in accordance with section 552(a)(4)(A) of title 5, United States Code,
to recover all reasonable costs incurred in processing requests made under section 552 of title
5, United States Code, for records obtained or created under this Act or any other Federal law
for which responsibility for administration has been delegated to the Commissioner by the
Secretary;
(2) retain all fees charged for such requests; and
(3) establish an accounting system and procedures to control receipts and expenditures of
fees received under this section.
(b) USE OF FEES. The Secretary and the Commissioner of Food and Drugs shall not use fees
received under this section for any purpose other than funding the processing of requests
described in subsection (a)(1). Such fees shall not be used to reduce the amount of funds
made to carry out other provisions of this Act.
(c) WAIVER OF FEES. Nothing in this section shall supersede the right of a requester to
obtain a waiver of fees pursuant to section 552(a)(4)(A) of title 5, United States Code.
PART 2 FEES RELATING TO DRUGS
SEC. 735. [ 21 U.S.C. 379g] DEFINITIONS. 1
For purposes of this subchapter:
(1) The term "human drug application" means an application for
(A) approval of a new drug submitted under section 505(b)(1),
(B) approval of a new drug submitted under section 505(b)(2) after September 30, 1992, which
requests approval of
(i) a molecular entity which is an active ingredient (including any salt or ester of an active
ingredient), or
(ii) an indication for a use,that had not been approved under an application submitted under
section 505(b), or
(C) licensure of a biological product under section 351 of the Public Health Service Act.
Such term does not include a supplement to such an application, does not include an
application with respect to whole blood or a blood component for transfusion, does not include
an application with respect to a bovine blood product for topical application licensed before
September 1, 1992, an allergenic extract product, or an in vitro diagnostic biologic product
licensed under section 351 of the Public Health Service Act, does not include an application
with respect to a large volume parenteral drug product approved before September 1, 1992,
does not include an application for a licensure of a biological product for further manufacturing
use only, and does not include an application or supplement submitted by a State or Federal
Government entity for a drug that is not distributed commercially. Such term does include an
application for licensure, as described in subparagraph (C), of a large volume biological
product intended for single dose injection for intravenous use or infusion.
(2) The term "supplement" means a request to the Secretary to approve a change in a human
drug application which has been approved.
(3) The term "prescription drug product" means a specific strength or potency of a drug in final
dosage form
(A) for which a human drug application has been approved,
(B) which may be dispensed only under prescription pursuant to section 503(b) , and
(C) which is on the list of products described in section 505(j)(7)(A) or is on a list created and
maintained by the Secretary of products approved under human drug applications under
section 351 of the Public Health Service Act.
Such term does not include whole blood or a blood component for transfusion, does not
include a bovine blood product for topical application licensed before September 1, 1992, an
allergenic extract product, or an in vitro diagnostic biologic product licensed under section 351
of the Public Health Service Act. Such term does not include a biological product that is
licensed for further manufacturing use only, and does not include a drug that is not distributed
commercially and is the subject of an application or supplement submitted by a State or
Federal Government entity. Such term does include a large volume biological product intended
for single dose injection for intravenous use or infusion.
(4) The term "final dosage form" means, with respect to a prescription drug product, a finished
dosage form which is approved for administration to a patient without substantial further
manufacturing.
(5) The term "prescription drug establishment" means a foreign or domestic place of business
which is at one general physical location consisting of one or more buildings all of which are
within five miles of each other and at which one or more prescription drug products are
manufactured in final dosage form. For purposes of this paragraph, the term "manufactured"
does not include packaging.
(6) The term "process for the review of human drug applications" means the following activities
of the Secretary with respect to the review of human drug applications and supplements:
(A) The activities necessary for the review of human drug applications and supplements.
(B) The issuance of action letters which approve human drug applications or which set forth in
detail the specific deficiencies in such applications and, where appropriate, the actions
necessary to place such applications in condition for approval.
(C) The inspection of prescription drug establishments and other facilities undertaken as part
of the Secretary’s review of pending human drug applications and supplements.
(D) Activities necessary for the review of applications for licensure of establishments subject to
section 351 of the Public Health Service Act and for the release of lots of biologics under such
section.
(E) Monitoring of research conducted in connection with the review of human drug
applications.
(F) In the case of drugs approved after October 1, 2002 , under human drug applications or
supplements: collecting, developing, and reviewing safety information on the drugs, including
adverse event reports, during a period of time after approval of such applications or
supplements, not to exceed three years.
(7) The term "costs of resources allocated for the process for the review of human drug
applications" means the expenses incurred in connection with the process for the review of
human drug applications for
(A) officers and employees of the Food and Drug Administration, contractors of the Food and
Drug Administration, advisory committees, and costs related to such officers, employees, and
committees and to contracts with such contractors,
(B) management of information, and the acquisition, maintenance, and repair of computer
resources,
(C) leasing, maintenance, renovation, and repair of facilities and acquisition, maintenance, and
repair of fixtures, furniture, scientific equipment, and other necessary materials and supplies,
and
(D) collecting fees under section 736 and accounting for resources allocated for the review of
human drug applications and supplements.
(8) The term "adjustment factor" applicable to a fiscal year for all urban consumers (all items;
United States city average) for April of the preceding fiscal year divided by such Index for April
1997.
(9) The term "affiliate" means a business entity that has a relationship with a second business
entity if, directly or indirectly
(A) one business entity controls, or has the power to control, the other business entity; or
(B) a third party controls, or has power to control, both of the business entities.
SEC. 736. [ 21 U.S.C. 379h] AUTHORITY TO ASSESS AND USE DRUG FEES. 2
(a) TYPES OF FEES.Beginning in fiscal year 2003, the Secretary shall assess and collect fees
in accordance with this section as follows:
(1) HUMAN DRUG APPLICATION AND SUPPLEMENT FEE.
(A) IN GENERAL. Each person that submits, on or after September 1, 1992, a human drug
application or a supplement shall be subject to a fee as follows:
(i) A fee established under subsection (c)(4) for a human drug application for which clinical
data (other than bioavailability or bioequivalence studies) with respect to safety or
effectiveness are required for approval.
(ii) A fee established under subsection (c)(4) for a human drug application for which clinical
data with respect to safety or effectiveness are not required or a supplement for which clinical
data (other than bioavailability or bioequivalence studies) with respect to safety or
effectiveness are required. Such fee shall be half of the amount of the fee established under
clause (i).
(B) PAYMENT. The fee required by subparagraph (A) shall be due upon submission of the
application or supplement.
(C) EXCEPTION FOR PREVIOUSLY FILED APPLICATION OR SUPPLEMENT. If a human
drug application or supplement was submitted by a person that paid the fee for such
application or supplement, was accepted for filing, and was not approved or was withdrawn
(without a waiver), the submission of a human drug application or a supplement for the same
product by the same person (or the person’s licensee, assignee, or successor) shall not be
subject to a fee under subparagraph (A).
(D) REFUND OF FEE IF APPLICATION REFUSED FOR FILING. The Secretary shall refund
75 percent of the fee paid under subparagraph (B) for any application or supplement which is
refused for filing.
(E) EXCEPTION FOR DESIGNATED ORPHAN DRUG OR INDICATION. A human drug
application for a prescription drug product that has been designated as a drug for a rare
disease or condition pursuant to section 526 shall not be subject to a fee under subparagraph
(A), unless the human drug application includes an indication for other than a rare disease or
condition. A supplement proposing to include a new indication for a rare disease or condition in
a human drug application shall not be subject to a fee under subparagraph (A), if the drug has
been designated pursuant to section 526 as a drug for a rare disease or condition with regard
to the indication proposed in such supplement.
(F) REFUND OF FEE IF APPLICATION WITHDRAWN. If an application or supplement is
withdrawn after the application or supplement was filed, the Secretary may refund the fee or a
portion of the fee if no substantial work was performed on the application or supplement after
the application or supplement was filed. The Secretary shall have the sole discretion to refund
a fee or a portion of the fee under this subparagraph. A determination by the Secretary
concerning a refund under this paragraph shall not be reviewable.
(2) PRESCRIPTION DRUG ESTABLISHMENT FEE.
(A) IN GENERAL. Except as provided in subparagraph (B), each person that
(i) is named as the applicant in a human drug application; and
(ii) after September 1, 1992, had pending before the Secretary a human drug application or
supplement,
shall be assessed an annual fee established under subsection (c)(4) for each prescription drug
establishment listed in its approved human drug application as an establishment that
manufactures the prescription drug product named in the application. The annual
establishment fee shall be assessed in each fiscal year in which the prescription drug product
named in the application is assessed a fee under paragraph (3) unless the prescription drug
establishment listed in the application does not engage in the manufacture of the prescription
drug product during the fiscal year. The establishment fee shall be payable on or before
October 1 of each year. Each such establishment shall be assessed only one fee per
establishment, notwithstanding the number of prescription drug products manufactured at the
establishment. In the event an establishment is listed in a human drug application by more
than one applicant, the establishment fee for the fiscal year shall be divided equally and
assessed among the applicants whose prescription drug products are manufactured by the
establishment during the fiscal year and assessed product fees under paragraph (3).
(B) EXCEPTION. If, during the fiscal year, an applicant initiates or causes to be initiated the
manufacture of a prescription drug product at an establishment listed in its human drug
application
(i) that did not manufacture the product in the previous fiscal year; and
(ii) for which the full establishment fee has been assessed in the fiscal year at a time before
manufacture of the prescription drug product was begun; the applicant will not be assessed a
share of the establishment fee for the fiscal year in which the manufacture of the product
began.
(3) PRESCRIPTION DRUG PRODUCT FEE.
(A) IN GENERAL. Except as provided in subparagraph (B), each person who is named as the
applicant in a human drug application, and who, after September 1, 1992, had pending before
the Secretary a human drug application or supplement, shall pay for each such prescription
drug product the annual fee established under subsection (c)(4). Such fee shall be payable on
or before October 1 of each year. Such fee shall be paid only once for each product for a fiscal
year in which the fee is payable.
(B) EXCEPTION. A prescription drug product shall not be assessed a fee under subparagraph
(A) if such product is identified on the list compiled under section 505(j)(7)(A) with a potency
described in terms of per 100 mL, or if such product is the same product as another product
approved under an application filed under section 505(b) or 505(j), under an abbreviated
application filed under section 507 3 (as in effect on the day before the date of enactment of
the Food and Drug Administration Modernization Act of 1997), or under an abbreviated new
drug application pursuant to regulations in effect prior to the implementation of the Drug Price
Competition and Patent Term Restoration Act of 1984.
(b) FEE REVENUE AMOUNTS. Except as provided in subsections (c), (d), (f), and (g), fees
under subsection (a) shall be established to generate the following revenue amounts:
Type of Fee Revenue Fiscal Year
2003
Fiscal Year
2004
Fiscal Year
2005
Fiscal Year
2006
Fiscal Year
2007
Application/Supplement $74,300,000 $77,000,000 $84,000,000 $86,434,000 $86,434,000
Establishment $74,300,000 $77,000,000 $84,000,000 $86,433,000 $86,433,000
Product $74,300,000 $77,000,000 $84,000,000 $86,433,000 $86,433,000
Total Fee Revenue $222,900,000 $231,000,000 $252,000,000 $259,300,000 $259,300,000
If, after the date of the enactment of the Prescription Drug User Fee Amendments of 2002 4 ,
legislation is enacted requiring the Secretary to fund additional costs of the retirement of
Federal personnel, fee revenue amounts shall be increased in each year by the amount
necessary to fully fund the portion of such additional costs that are attributable to the process
for the review of human drug applications.
(c) ADJUSTMENTS.
(1) INFLATION ADJUSTMENT. Revenues established in subsection (b) shall be adjusted by
the Secretary by notice, published in the Federal Register, for a fiscal year to reflect the
greater of
(A) the total percentage change that occurred in the Consumer Price Index for all urban
consumers (all items; U.S. city average), for the 12 month period ending June 30 preceding
the fiscal year for which fees are being established, or
(B) the total percentage change for the previous fiscal year in basic pay under the General
Schedule in accordance with section 5332 of title 5, United States Code, as adjusted by any
locality-based comparability payment pursuant to section 5304 of such title for Federal
employees stationed in the District of Columbia.
The adjustment made each fiscal year by this subsection will be added on a compounded
basis to the sum of all adjustments made each fiscal year after for fiscal year 2003 under this
subsection.
(2) WORKLOAD ADJUSTMENT. Beginning with fiscal year 2004, after the fee revenues
established in subsection (b) are adjusted for a fiscal year for inflation in accordance with
paragraph (1), the fee revenues shall be adjusted further for such fiscal year to reflect changes
in the workload of the Secretary for the process for the review of human drug applications.
With respect to such adjustment:
(A) The adjustment shall be determined by the Secretary based on a weighted average of the
change in the total number of human drug applications, commercial investigational new drug
applications, efficacy supplements, and manufacturing supplements submitted to the
Secretary. The Secretary shall publish in the Federal Register the fee revenues and fees
resulting from the adjustment and the supporting methodologies.
(B) Under no circumstances shall the adjustment result in fee revenues for a fiscal year that
are less than the fee revenues for the fiscal year established in subsection (b), as adjusted for
inflation under paragraph (1).
(3) FINAL YEAR ADJUSTMENT. For fiscal year 2007, the Secretary may, in addition to
adjustments under paragraphs (1) and (2), further increase the fee revenues and fees
established in subsection (b) if such an adjustment is necessary to provide for not more than
three months of operating reserves of carryover user fees for the process for the review of
human drug applications for the first three months of fiscal year 2008. If such an adjustment is
necessary, the rationale for the amount of the increase shall be contained in the annual notice
establishing fee revenues and fees for fiscal year 2007. If the Secretary has carryover
balances for such process in excess of three months of such operating reserves, the
adjustment under this paragraph shall not be made.
(4) ANNUAL FEE SETTING. The Secretary shall, 60 days before the start of each fiscal year
that begins after September 30, 2002, establish, for the next fiscal year, application, product,
and establishment fees under subsection (a), based on the revenue amounts established
under subsection (b) and the adjustments provided under this subsection.
( 5) LIMIT. The total amount of fees charged, as adjusted under this subsection, for a fiscal
year may not exceed the total costs for such fiscal year for the resources allocated for the
process for the review of human drug applications.
(d) FEE WAIVER OR REDUCTION.
(1) IN GENERAL. The Secretary shall grant a waiver from or a reduction of one or more fees
assessed under subsection (a) where the Secretary finds that
(A) such waiver or reduction is necessary to protect the public health,
(B) the assessment of the fee would present a significant barrier to innovation because of
limited resources available to such person or other circumstances,
(C) the fees to be paid by such person will exceed the anticipated present and future costs
incurred by the Secretary in conducting the process for the review of human drug applications
for such person, or
( D) the applicant involved is a small business submitting its first human drug application to the
Secretary for review.
(2) USE OF STANDARD COSTS. In making the finding in paragraph (1)(C), the Secretary
may use standard costs.
(3) RULES RELATING TO SMALL BUSINESSES.
(A) DEFINITION. In paragraph (1)(D), the term "small business" means an entity that has
fewer than 500 employees, including employees of affiliates.
(B) WAIVER OF APPLICATION FEE. The Secretary shall waive under paragraph (1)(D) the
application fee for the first human drug application that a small business or its affiliate submits
to the Secretary for review. After a small business or its affiliate is granted such a waiver, the
small business or its affiliate shall pay
(i) application fees for all subsequent human drug applications submitted to the Secretary for
review in the same manner as an entity that does not qualify as a small business; and
(ii) all supplement fees for all supplements to human drug applications submitted to the
Secretary for review in the same manner as an entity that does not qualify as a small business.
(e) EFFECT OF FAILURE TO PAY FEES. A human drug application or supplement submitted
by a person subject to fees under subsection (a) shall be considered incomplete and shall not
be accepted for filing by the Secretary until all fees owed by such person have been paid.
(f) LIMITATIONS.
(1) IN GENERAL. Fees under subsection (a) shall be refunded for a fiscal year beginning after
fiscal year 1997 unless appropriations for salaries and expenses of the Food and Drug
Administration for such fiscal year (excluding the amount of fees appropriated for such fiscal
year) are equal to or greater than the amount of appropriations for the salaries and expenses
of the Food and Drug Administration for the fiscal year 1997 (excluding the amount of fees
appropriated for such fiscal year) multiplied by the adjustment factor applicable to the fiscal
year involved.
(2) AUTHORITY. If the Secretary does not assess fees under subsection (a) during any
portion of a fiscal year because of paragraph (1) and if at a later date in such fiscal year the
Secretary may assess such fees, the Secretary may assess and collect such fees, without any
modification in the rate, for human drug applications and supplements, prescription drug
establishments, and prescription drug products at any time in such fiscal year notwithstanding
the provisions of subsection (a) relating to the date fees are to be paid.
(g) CREDITING AND AVAILABILITY OF FEES.
(1) IN GENERAL. Fees collected for a fiscal year pursuant to subsection (a) shall be credited
to the appropriation account for salaries and expenses of the Food and Drug Administration
and shall be available in accordance with appropriation Acts until expended without fiscal year
limitation. 5 Such sums as may be necessary may be transferred from the Food and Drug
Administration salaries and expenses appropriation account without fiscal year limitation to
such appropriation account for salaries and expenses with such fiscal year limitation. The
sums transferred shall be available solely for the process for the review of human drug
applications.
(2) COLLECTIONS AND APPROPRIATION ACTS.
(A) IN GENERAL. The fees authorized by this section
(i) shall be retained in each fiscal year in an amount not to exceed the amount specified in
appropriation Acts, or otherwise made available for obligation, for such fiscal year, and
(ii) shall only be collected and available to defray increases in the costs of the resources
allocated for the process for the review of human drug applications (including increases in
such costs for an additional number of fulltime equivalent positions in the Department of Health
and Human Services to be engaged in such process) over such costs, excluding costs paid
from fees collected under this section, for fiscal year 1997 multiplied by the adjustment factor.
(B) COMPLIANCE. The Secretary shall be considered to have met the requirements of
subparagraph (A)(ii) in any fiscal year if the costs funded by appropriations and allocated for
the process for the review of human drug applications
(i) are not more than 3 percent below the level specified in subparagraph (A)(ii); or
(ii)(I) are more than 3 percent below the level specified in subparagraph (A)(ii), and fees
assessed for the fiscal year following the subsequent fiscal year are decreased by the amount
in excess of 3 percent by which such costs fell below the level specified in such subparagraph;
and
(II) such costs are not more than 5 percent below the level specified in such subparagraph.
(3) AUTHORIZATION OF APPROPRIATIONS. There are authorized to be appropriated for
fees under this section
(A) $222,900,000 for fiscal year 2003;
(B) $231,000,000 for fiscal year 2004;
(C) $252,000,000 for fiscal year 2005;
(D) $259,300,000 for fiscal year 2006; and
(E) $259,300,000 for fiscal year 2007;
as adjusted to reflect adjustments in the total fee revenues made under this section and
changes in the total amounts collected by application, supplement, establishment, and product
fees.
(4) OFFSET. Any amount of fees collected for a fiscal year under this section that exceeds the
amount of fees specified in appropriation Acts for such fiscal year shall be credited to the
appropriation account of the Food and Drug Administration as provided in paragraph (1), and
shall be subtracted from the amount of fees that would otherwise be authorized to be collected
under this section pursuant to appropriation Acts for a subsequent fiscal year.
(h) COLLECTION OF UNPAID FEES. In any case where the Secretary does not receive
payment of a fee assessed under subsection (a) within 30 days after it is due, such fee shall be
treated as a claim of the United States Government subject to subchapter II of chapter 37 of
title 31, United States Code.
(i) WRITTEN REQUESTS FOR WAIVERS, REDUCTIONS, AND REFUNDS. To qualify for
consideration for a waiver or reduction under subsection (d), or for a refund of any fee
collected in accordance with subsection (a), a person shall submit to the Secretary a written
request for such waiver, reduction, or refund not later than 180 days after such fee is due.
(j) CONSTRUCTION. This section may not be construed to require that the number of full-time
equivalent positions in the Department of Health and Human Services, for officers, employers,
and advisory committees not engaged in the process of the review of human drug applications,
be reduced to offset the number of officers, employees, and advisory committees so engaged.
PART 3--FEES RELATING TO DEVICES
SEC. 737. [21 U.S.C. 379i] DEFINITIONS 6
For purposes of this subchapter:
(1) The term 'premarket application' means-- (A) an application for approval of a device
submitted under section 515(c) or section 351 of the Public Health Service Act; or (B) a
product development protocol described in section 515(f). Such term does not include a
supplement, a premarket report, or a premarket notification submission.
(2) The term 'premarket report' means a report submitted under section 515(c)(2).
(3) The term 'premarket notification submission' means a report submitted under section
510(k).
(4)(A) The term 'supplement', with respect to a panel-track supplement, a 180-day supplement,
a real-time supplement, or an efficacy supplement, means a request to the Secretary to
approve a change in a device for which--
(i) an application or report has been approved under section 515(d), or an application has
been approved under section 351 of the Public Health Service Act; or
(ii) a notice of completion has become effective under section 515(f).
(B) The term 'panel-track supplement' means a supplement to an approved premarket
application or premarket report under section 515 that requests a significant change in design
or performance of the device, or a new indication for use of the device, and for which
substantial clinical data are necessary to provide a reasonable assurance of safety and
effectiveness.
(C) The term '180-day supplement' means a supplement to an approved premarket application
or premarket report under section 515 that is not a panel-track supplement and requests a
significant change in components, materials, design, specification, software, color additives, or
labeling.
(D) The term 'real-time supplement' means a supplement to an approved premarket
application or premarket report under section 515 that requests a minor change to the device,
such as a minor change to the design of the device, software, sterilization, or labeling, and for
which the applicant has requested and the agency has granted a meeting or similar forum to
jointly review and determine the status of the supplement.
(E) The term 'efficacy supplement' means a supplement to an approved premarket application
under section 351 of the Public Health Service Act that requires substantive clinical data.
(5) The term 'process for the review of device applications' means the following activities of the
Secretary with respect to the review of premarket applications, premarket reports,
supplements, and premarket notification submissions:
(A) The activities necessary for the review of premarket applications, premarket reports,
supplements, and premarket notification submissions.
(B) The issuance of action letters that allow the marketing of devices or which set forth in detail
the specific deficiencies in such applications, reports, supplements, or submissions and,
where appropriate, the actions necessary to place them in condition for approval.
(C) The inspection of manufacturing establishments and other facilities undertaken as part of
the Secretary's review of pending premarket applications, premarket reports, and
supplements.
(D) Monitoring of research conducted in connection with the review of such applications,
reports, supplements, and submissions.
(E) Review of device applications subject to section 351 of the Public Health Service Act for an
investigational new drug application under section 505(i) or for an investigational device
exemption under section 520(g) and activities conducted in anticipation of the submission of
such applications under section 505(i) or 520(g).
(F) The development of guidance, policy documents, or regulations to improve the process for
the review of premarket applications, premarket reports, supplements, and premarket
notification submissions.
(G) The development of voluntary test methods, consensus standards, or mandatory
performance standards under section 514 in connection with the review of such applications,
reports, supplements, or submissions and related activities.
(H) The provision of technical assistance to device manufacturers in connection with the
submission of such applications, reports, supplements, or submissions.
(I) Any activity undertaken under section 513 or 515(i) in connection with the initial
classification or reclassification of a device or under section 515(b) in connection with any
requirement for approval of a device.
(J) Evaluation of postmarket studies required as a condition of an approval of a premarket
application or premarket report under section 515 or a premarket application under section
351 of the Public Health Service Act.
(K) Compiling, developing, and reviewing information on relevant devices to identify safety and
effectiveness issues for devices subject to premarket applications, premarket reports,
supplements, or premarket notification submissions.
(6) The term "costs of resources allocated for the process for the review of device applications"
means the expenses incurred in connection with the process for the review of device
applications for--
(A) officers and employees of the Food and Drug Administration, contractors of the Food and
Drug Administration, advisory committees, and costs related to such officers, employees, and
committees and to contracts with such contractors;
(B) management of information, and the acquisition, maintenance, and repair of computer
resources;
(C) leasing, maintenance, renovation, and repair of facilities and acquisition, maintenance, and
repair of fixtures, furniture, scientific equipment, and other necessary materials and supplies;
and
(D) collecting fees and accounting for resources allocated for the review of premarket
applications, premarket reports, supplements, and submissions.
(7) The term 'adjustment factor' applicable to a fiscal year is the Consumer Price Index for all
urban consumers (all items; United States city average) for April of the preceding fiscal year
divided by such Index for April 2002.
(8) The term 'affiliate' means a business entity that has a relationship with a second business
entity (whether domestic or international) if, directly or indirectly--
(A) one business entity controls, or has the power to control, the other business entity; or
(B) a third party controls, or has power to control, both of the business entities.
SEC. 738. [21 U.S.C. 379j] AUTHORITY TO ASSESS AND USE DEVICE FEES. 7
(a) TYPES OF FEES.
(1) IN GENERAL. Beginning on the date of the enactment of the Medical Device User Fee and
Modernization Act of 2002 [enacted Oct. 26, 2002]8 , the Secretary shall assess and collect
fees in accordance with this section.
(2) PREMARKET APPLICATION, PREMARKET REPORT, SUPPLEMENT, AND
SUBMISSION FEE.--
(A) IN GENERAL.--Except as provided in subparagraph (B) and subsections (d) and (e), each
person who submits any of the following, on or after October 1, 2002, shall be subject to a fee
established under subsection (c)(1) for the fiscal year involved in accordance with the
following:
(i) A premarket application.
(ii) For a premarket report, a fee equal to the fee that applies under clause (i).
(iii) For a panel track supplement, a fee equal to the fee that applies under clause (i).
(iv) For a 180-day supplement, a fee equal to 21.5 percent of the fee that applies under clause
(i).
(v) For a real-time supplement, a fee equal to 7.2 percent of the fee that applies under clause
(i).
(vi) For an efficacy supplement, a fee equal to the fee that applies under clause (i).
(vii) For a premarket notification submission, a fee equal to 1.42 percent of the fee that applies
under clause (i), subject to any adjustment under subsection (e)(2)(C)(ii).
(B) EXCEPTIONS.--
(i) HUMANITARIAN DEVICE EXEMPTION.--An application under section 520(m) is not
subject to any fee under subparagraph (A).
(ii) FURTHER MANUFACTURING USE.--No fee shall be required under subparagraph (A) for
the submission of a premarket application under section 351 of the Public Health Service Act
[42 USCS § 262] for a product licensed for further manufacturing use only.
(iii) STATE OR FEDERAL GOVERNMENT SPONSORS.--No fee shall be required under
subparagraph (A) for a premarket application, premarket report, supplement, or premarket
notification submission submitted by a State or Federal Government entity unless the device
involved is to be distributed commercially.
(iv) PREMARKET NOTIFICATIONS BY THIRD PARTIES.--No fee shall be required under
subparagraph (A) for a premarket notification submission reviewed by an accredited person
pursuant to section 523.
(v) PEDIATRIC CONDITIONS OF USE.
(I) IN GENERAL.--No fee shall be required under subparagraph (A) for a premarket application,
premarket report, or premarket notification submission if the proposed conditions of use for the
device involved are solely for a pediatric population. No fee shall be required under such
subparagraph for a supplement if the sole purpose of the supplement is to propose conditions
of use for a pediatric population.
(II) SUBSEQUENT PROPOSAL OF ADULT CONDITIONS OF USE.--In the case of a person
who submits a premarket application or premarket report for which, under subclause (I), a fee
under subparagraph (A) is not required, any supplement to such application that proposes
conditions of use for any adult population is subject to the fee that applies under such
subparagraph for a premarket application.
(C) PAYMENT.--The fee required by subparagraph (A) shall be due upon submission of the
premarket application, premarket report, supplement, or premarket notification submission
except that invoices for applications submitted between October 1, 2002, and the date of the
enactment of the Medical Device User Fee and Modernization Act of 2002 [enacted Oct. 26,
2002]9 shall be payable on October 30, 2002. Applicants submitting portions of applications
pursuant to section 515(c)(3) shall pay such fees upon submission of the first portion of such
applications. The fees credited to fiscal year 2003 under this section shall include all fees
payable from October 1, 2002 , through September 30, 2003 .
(D) REFUNDS.
(i) APPLICATION REFUSED FOR FILING.--The Secretary shall refund 75 percent of the fee
paid under subparagraph (A) for any application, report, or supplement that is refused for filing.
(ii) APPLICATION WITHDRAWN BEFORE FILING--The Secretary shall refund 75 percent of
the fee paid under subparagraph (A) for any application, report, or supplement that is
withdrawn prior to the filing decision of the Secretary.
(iii) APPLICATION WITHDRAWN BEFORE FIRST ACTION.--After receipt of a request for a
refund of the fee paid under subparagraph (A) for a premarket application, premarket report, or
supplement that is withdrawn after filing but before a first action, the Secretary may return
some or all of the fee. The amount of refund, if any, shall be based on the level of effort already
expended on the review of such application, report, or supplement. The Secretary shall have
sole discretion to refund a fee or portion of the fee under this subparagraph. A determination
by the Secretary concerning a refund under this paragraph shall not be reviewable.
(b) FEE REVENUE AMOUNTS.--Except as provided in subsections (c), (d), (e), (g), and (h),
the fees under subsection (a) shall be established to generate the following revenue amounts:
$25,125,000 in fiscal year 2003; $27,255,000 in fiscal year 2004; and $29,785,000 in fiscal
year 2005. If legislation is enacted after the date of the enactment of the Medical Device User
Fee and Modernization Act of 2002 [enacted Oct. 26, 2002] requiring the Secretary to fund
additional costs of the retirement of Federal personnel, fee revenue amounts under this
subsection shall be increased in each year by the amount necessary to fully fund the portion of
such additional costs that are attributable to the process for the review of device applications.
(c) ANNUAL FEE SETTING.
(1) In general. The Secretary shall, 60 days before the start of each fiscal year after September
30, 2002, publish in the Federal Register fees under subsection (a). The fees established for
fiscal year 2006 shall be based on a premarket application fee of $ 259,600, and the fees
established for fiscal year 2007 shall be based on a premarket application fee of $ 281,600.
(2) Limit. The total amount of fees charged, as adjusted under this subsection, for a fiscal year
may not exceed the total costs for such fiscal year for the resources allocated for the process
for the review of device applications.
(3) Supplement.
(A) In general. For fiscal years 2006 and 2007, the Secretary may use unobligated carryover
balances from fees collected in previous fiscal years to ensure that sufficient fee revenues are
available in that fiscal year, so long as the Secretary maintains unobligated carryover balances
of not less than 1 month of operating reserves for the first month of fiscal year 2008.
(B) Notice to Congress. Not later than 14 days before the Secretary anticipates the use of
funds described in subparagraph (A), the Secretary shall provide notice to the Committee on
Health, Education, Labor, and Pensions and the Committee on Appropriations of the Senate
and the Committee on Energy and Commerce and the Committee on Appropriations of the
House of Representatives.
(d) SMALL BUSINESSES; FEE WAIVER AND FEE REDUCTION REGARDING
PREMARKET APPROVAL FEES.--
(1) IN GENERAL.--The Secretary shall grant a waiver of the fee required under subsection (a)
for one premarket application, or one premarket report, where the Secretary finds that the
applicant involved is a small business submitting its first premarket application to the Secretary,
or its first premarket report, respectively, for review. For the purposes of this paragraph, the
term "small business" means an entity that reported $ 30,000,000 or less of gross receipts or
sales in its most recent Federal income tax return for a taxable year, including such returns of
all of its affiliates, partners, and parent firms. In addition, for subsequent premarket
applications, premarket reports, and supplements where the Secretary finds that the applicant
involved is a small business, the fees specified in clauses (i) through (vi) of subsection (a)(2)(A)
may be paid at a reduced rate in accordance with paragraph (2)(C).
(2) RULES RELATING TO PRMARKET APPROVAL FEES.--
(A) DEFINITION. For purposes of this paragraph, the term "small business" means an entity
that reported $ 100,000,000 or less of gross receipts or sales in its most recent Federal income
tax return for a taxable year, including such returns of all of its affiliates, partners, and parent
firms.
(B) EVIDENCE OF QUALIFICATION.--An applicant shall pay the higher fees established by
the Secretary each year unless the applicant submits evidence that it qualifies for a waiver of
the fee or the lower fee rate. The applicant shall support its claim that it meets the definition
under subparagraph (A) by submission of a copy of its most recent Federal income tax return
for a taxable year, and a copy of such returns of its affiliates, partners, and parent firms, which
show an amount of gross sales or receipts that is less than the maximum established in
subparagraph (A). The applicant, and each of such affiliates, partners, and parent firms, shall
certify that the information provided is a true and accurate copy of the actual tax forms they
submitted to the Internal Revenue Service. If no tax forms are submitted for affiliates, partners,
or parent firms, the applicant shall certify that the applicant has no affiliates, partners, or parent
firms, respectively.
(C) REDUCED FEES.--Where the Secretary finds that the applicant involved meets the
definition under subparagraph (A), the fees established under subsection (c)(1) may be paid at
a reduced rate of 38 percent of the fee established under such subsection for a premarket
application, a premarket report, or a supplement.
(D) REQUEST FOR FEE WAIVER OR REDUCTION.--An applicant seeking a fee waiver or
reduction under this subsection shall submit supporting information to the Secretary at least 60
days before the fee is required pursuant to subsection (a). The decision of the Secretary
regarding whether an entity qualifies for such a waiver or reduction is not reviewable.
(e) SMALL BUSINESSES; FEE REDUCTION REGARDING PREMARKET NOTIFICATION
SUBMISSIONS.--
(1) IN GENERAL.--For fiscal year 2004 and each subsequent fiscal year, where the Secretary
finds that the applicant involved is a small business, the fee specified in subsection (a)(2)(A)(vii)
may be paid at a reduced rate in accordance with paragraph (2)(C).
(2) RULES RELATING TO PREMARKET NOTIFICATION SUBMISSIONS.--
(A) DEFINITION.--For purposes of this subsection, the term 'small business' means an entity
that reported $100,000,000 or less of gross receipts or sales in its most recent Federal income
tax return for a taxable year, including such returns of all of its affiliates, partners, and parent
firms.
(B) EVIDENCE OF QUALIFICATION.--An applicant shall pay the higher fees established by
the Secretary each year unless the applicant submits evidence that it qualifies for the lower fee
rate. The applicant shall support its claim that it meets the definition under subparagraph (A)
by submission of a copy of its most recent Federal income tax return for a taxable year, and a
copy of such returns of its affiliates, partners, and parent firms, which show an amount of gross
sales or receipts that is less than the maximum established in subparagraph (A). The applicant,
and each of such affiliates, partners, and parent firms, shall certify that the information
provided is a true and accurate copy of the actual tax forms they submitted to the Internal
Revenue Service. If no tax forms are submitted for affiliates, partners, or parent firms, the
applicant shall certify that the applicant has no affiliates, partners, or parent firms, respectively.
(C) REDUCED FEES.--
(i) IN GENERAL.--For fiscal year 2004 and each subsequent fiscal year, where the Secretary
finds that the applicant involved meets the definition under subparagraph (A), the fee for a
premarket notification submission may be paid at 80 percent of the fee that applies under
subsection (a)(2)(A)(vii), as adjusted under clause (ii) and as established under subsection
(c)(1).
(ii) ADJUSTMENT PER FEE REVENUE AMOUNT.--For fiscal year 2004 and each
subsequent fiscal year, the Secretary, in setting the revenue amount under subsection (c)(1)
for premarket notification submissions, shall determine the revenue amount that would apply if
all such submissions for the fiscal year involved paid a fee equal to 1.42 percent of the amount
that applies under subsection (a)(2)(A)(i) for premarket applications, and shall adjust the fee
under subsection (a)(2)(A)(vii) for premarket notification submissions such that the reduced
fees collected under clause (i) of this subparagraph, when added to fees for such submissions
that are not paid at the reduced rate, will equal such revenue amount for the fiscal year.
(D) REQUEST FOR REDUCTION.--An applicant seeking a fee reduction under this
subsection shall submit supporting information to the Secretary at least 60 days before the fee
is required pursuant to subsection (a). The decision of the Secretary regarding whether an
entity qualifies for such a reduction is not reviewable.
(f) EFFECT OF FAILURE TO PAY FEES.--A premarket application, premarket report,
supplement, or premarket notification submission submitted by a person subject to fees under
subsection (a) shall be considered incomplete and shall not be accepted by the Secretary until
all fees owed by such person have been paid.
(g) CONDITIONS.--
(1) PERFORMANCE GOALS THROUGH FISCAL YEAR 2005; TERMINATION OF
PROGRAM AFTER FISCAL YEAR 2005.--With respect to the amount that, under the salaries
and expenses account of the Food and Drug Administration, is appropriated for a fiscal year
for devices and radiological products:
(A)(i) For each of the fiscal years 2003 and 2004, the Secretary is expected to meet all of the
goals identified for the fiscal year involved in any letter referred to in section 101(3) of the
Medical Device User Fee and Modernization Act of 2002 (referred to in this paragraph as
"performance goals") if the amount so appropriated for such fiscal year, excluding the amount
of fees appropriated for such fiscal year, is equal to or greater than $205,720,000 multiplied by
the adjustment factor applicable to the fiscal year.
(ii) For each of the fiscal years 2003 and 2004, if the amount so appropriated for the fiscal year
involved, excluding the amount of fees appropriated for such fiscal year, is less than the
amount that applies under clause (i) for such fiscal year, the following applies:
(I) The Secretary is expected to meet such goals to the extent practicable, taking into account
the amounts that are available to the Secretary for such purpose, whether from fees under
subsection (a) or otherwise.
(II) The Comptroller General of the United States shall submit to the Congress a report
describing whether and to what extent the Secretary is meeting the performance goals
identified for such fiscal year, and whether the Secretary will be able to meet all performance
goals identified for fiscal year 2005. A report under the preceding sentence shall be submitted
to the Congress not later than July 1 of the fiscal year with which the report is concerned.
(B)(i) For fiscal year 2005, the Secretary is expected to meet all of the performance goals
identified for the fiscal year if the amount so appropriated for such fiscal year, excluding the
amount of fees appropriated for such fiscal year, is equal to or greater than $205,720,000
multiplied by the adjustment factor applicable to the fiscal year.
(ii) For fiscal year 2005, if the amount so appropriated for such fiscal year, excluding the
amount of fees appropriated for such fiscal year, is more than 1 percent less than the amount
that applies under clause (i), the following applies:
(I) The Secretary is expected to meet such goals to the extent practicable, taking into account
the amounts that are available to the Secretary for such purpose, whether from fees under
subsection (a) or otherwise.
(II) The Comptroller General of the United States shall submit to the Congress a report
describing whether and to what extent the Secretary is meeting the performance goals
identified for such fiscal year, and whether the Secretary will be able to meet all performance
goals identified for fiscal year 2006. The report under the preceding sentence shall be
submitted to the Congress not later than July 1, 2005.
(C) For fiscal year 2006, fees may not be assessed under subsection (a) for the fiscal year,
and the Secretary is not expected to meet any performance goals identified for the fiscal year,
if the total of the amounts so appropriated for fiscal years 2005 and 2006, excluding the
amount of fees appropriated for such fiscal years, is more than 1 percent less than the sum
of--
(i) $205,720,000 multiplied by the adjustment factor applicable to fiscal year 2006; and
(ii) an amount equal to the amount that applies for purposes of subparagraph (B)(i).
(D) For fiscal year 2007, fees may not be assessed under subsection (a) for the fiscal year,
and the Secretary is not expected to meet any performance goals identified for the fiscal year,
if--
(i) the amount so appropriated for the fiscal year, excluding the amount of fees appropriated
for the fiscal year, is more than 1 percent less than $205,720,000 multiplied by the adjustment
factor applicable to fiscal year 2007; or
(ii) pursuant to subparagraph (C), fees were not assessed under subsection (a) for fiscal year
2006.
(2) AUTHORITY.--If the Secretary does not assess fees under subsection (a) during any
portion of a fiscal year because of subparagraph (C) or (D) of paragraph (1) and if at a later
date in such fiscal year the Secretary may assess such fees, the Secretary may assess and
collect such fees, without any modification in the rate for premarket applications, supplements,
premarket reports, and premarket notification submissions, and at any time in such fiscal year,
notwithstanding the provisions of subsection (a) relating to the date fees are to be paid.
(h) CREDITING AND AVAILABILITY OF FEES.--
(1) IN GENERAL.--Fees authorized under subsection (a) shall be collected and available for
obligation only to the extent and in the amount provided in advance in appropriation Acts. Such
fees are authorized to be appropriated to remain available until expended. Such sums as may
be necessary may be transferred from the Food and Drug Administration salaries and
expenses appropriation account without fiscal year limitation to such appropriation account for
salaries and expenses with such fiscal year limitation. The sums transferred shall be available
solely for the process for the review of device applications.
(2) COLLECTIONS AND APPROPRIATION ACTS.--
(A) IN GENERAL.--The fees authorized by this section--
(i) shall be retained in each fiscal year in an amount not to exceed the amount specified in
appropriation Acts, or otherwise made available for obligation, for such fiscal year, and
(ii) shall only be collected and available to defray increases in the costs of the resources
allocated for the process for the review of device applications (including increases in such
costs for an additional number of full-time equivalent positions in the Department of Health and
Human Services to be engaged in such process) over such costs, excluding costs paid from
fees collected under this section, for fiscal year 2002 multiplied by the adjustment factor.
(B) Compliance.
(i) In GENERAL. The Secretary shall be considered to have met the requirements of
subparagraph (A)(ii) in any fiscal year if the costs funded by appropriations and allocated for
the process for the review of device applications
(I) are not more than 3 percent below the level specified in subparagraph (A)(ii); or
(II)(aa) are more than 3 percent below the level specified in subparagraph (A)(ii), and fees
assessed for a subsequent fiscal year are decreased by the amount in excess of 3 percent by
which such costs fell below the level specified in such subparagraph; and
(bb) such costs are not more than 5 percent below the level specified in such subparagraph.
(ii) MORE THAN 5 PERCENT. To the extent such costs are more than 5 percent below the
specified level in subparagraph (A)(ii), fees may not collected under this section for that fiscal
year.
(3) AUTHORIZATION OF APPROPRIATIONS.--There are authorized to be appropriated for
fees under this section--
(A) $25,125,000 for fiscal year 2003;
(B) $27,255,000 for fiscal year 2004;
(C) $29,785,000 for fiscal year 2005; and
(D) such sums as may be necessary for each of fiscal years 2006 and 2007
as adjusted to reflect adjustments in the total fee revenues made under this section and
changes in the total amounts collected by application fees.
(4) OFFSET.--Any amount of fees collected for a fiscal year under this section that exceeds
the amount of fees specified in appropriation Acts for such fiscal year shall be credited to the
appropriation account of the Food and Drug Administration as provided in paragraph (1), and
shall be subtracted from the amount of fees that would otherwise be authorized to be collected
under this section pursuant to appropriation Acts for a subsequent fiscal year.
(i) COLLECTION OF UNPAID FEES.--In any case where the Secretary does not receive
payment of a fee assessed under subsection (a) within 30 days after it is due, such fee shall be
treated as a claim of the United States Government subject to subchapter II of chapter 37 of
title 31, United States Code.
(j) WRITTEN REQUESTS FOR REFUNDS.--To qualify for consideration for a refund under
subsection (a)(2)(D), a person shall submit to the Secretary a written request for such refund
not later than 180 days after such fee is due.
(k) CONSTRUCTION.--This section may not be construed to require that the number of
full-time equivalent positions in the Department of Health and Human Services, for officers,
employees, and advisory committees not engaged in the process of the review of device
applications, be reduced to offset the number of officers, employees, and advisory committees
so engaged.
PART 4 FEES RELATING TO ANIMAL DRUGS
SEC. 739. [21 U.S.C. 379j-11] DEFINITIONS.
For purposes of this subchapter:
(1) The term "animal drug application" means an application for approval of any new animal
drug submitted under section 512(b)(1). Such term does not include either a new animal drug
application submitted under section 512(b)(2) or a supplemental animal drug application.
(2) The term "supplemental animal drug application" means
(A) a request to the Secretary to approve a change in an animal drug application which has
been approved; or
(B) a request to the Secretary to approve a change to an application approved under section
512(c)(2) for which data with respect to safety or effectiveness are required.
(3) The term "animal drug product" means each specific strength or potency of a particular
active ingredient or ingredients in final dosage form marketed by a particular manufacturer or
distributor, which is uniquely identified by the labeler code and product code portions of the
national drug code, and for which an animal drug application or a supplemental animal drug
application has been approved.
(4) The term "animal drug establishment" means a foreign or domestic place of business which
is at one general physical location consisting of one or more buildings all of which are within 5
miles of each other, at which one or more animal drug products are manufactured in final
dosage form.
(5) The term "investigational animal drug submission" means
(A) the filing of a claim for an investigational exemption under section 512(j) for a new animal
drug intended to be the subject of an animal drug application or a supplemental animal drug
application, or
(B) the submission of information for the purpose of enabling the Secretary to evaluate the
safety or effectiveness of an animal drug application or supplemental animal drug application
in the event of their filing.
(6) The term "animal drug sponsor" means either an applicant named in an animal drug
application, except for an approved application for which all subject products have been
removed from listing under section 510, or a person who has submitted an investigational
animal drug submission that has not been terminated or otherwise rendered inactive by the
Secretary.
(7) The term "final dosage form" means, with respect to an animal drug product, a finished
dosage form which is approved for administration to an animal without substantial further
manufacturing. Such term includes animal drug products intended for mixing in animal feeds.
(8) The term "process for the review of animal drug applications" means the following activities
of the Secretary with respect to the review of animal drug applications, supplemental animal
drug applications, and investigational animal drug submissions:
(A) The activities necessary for the review of animal drug applications, supplemental animal
drug applications, and investigational animal drug submissions.
(B) The issuance of action letters which approve animal drug applications or supplemental
animal drug applications or which set forth in detail the specific deficiencies in animal drug
applications, supplemental animal drug applications, or investigational animal drug
submissions and, where appropriate, the actions necessary to place such applications,
supplements or submissions in condition for approval.
(C) The inspection of animal drug establishments and other facilities undertaken as part of the
Secretary’s review of pending animal drug applications, supplemental animal drug applications,
and investigational animal drug submissions.
(D) Monitoring of research conducted in connection with the review of animal drug applications,
supplemental animal drug applications, and investigational animal drug submissions.
(E) The development of regulations and policy related to the review of animal drug applications,
supplemental animal drug applications, and investigational animal drug submissions.
(F) Development of standards for products subject to review.
(G) Meetings between the agency and the animal drug sponsor.
(H) Review of advertising and labeling prior to approval of an animal drug application or
supplemental animal drug application, but not such activities after an animal drug has been
approved.
(9) The term "costs of resources allocated for the process for the review of animal drug
applications" means the expenses incurred in connection with the process for the review of
animal drug applications for
(A) officers and employees of the Food and Drug Administration, contractors of the Food and
Drug Administration, advisory committees consulted with respect to the review of specific
animal drug applications, supplemental animal drug applications, or investigational animal
drug submissions, and costs related to such officers, employees, committees, and contractors,
including costs for travel, education, and recruitment and other personnel activities,
(B) management of information, and the acquisition, maintenance, and repair of computer
resources,
(C) leasing, maintenance, renovation, and repair of facilities and acquisition, maintenance, and
repair of fixtures, furniture, scientific equipment, and other necessary materials and supplies,
and
(D) collecting fees under section 740 and accounting for resources allocated for the review of
animal drug applications, supplemental animal drug applications, and investigational animal
drug submissions.
(10) The term "adjustment factor" applicable to a fiscal year refers to the formula set forth in
section 735(8) with the base or comparator year being 2003.
(11) The term "affiliate" refers to the definition set forth in section 735(9).
SEC. 740. [21 U.S.C. 379j-12] AUTHORITY TO ASSESS AND USE ANIMAL DRUG FEES.
(a) TYPES OF FEES. Beginning in fiscal year 2004, the Secretary shall assess and collect
fees in accordance with this section as follows:
(1) ANIMAL DRUG APPLICATION AND SUPPLEMENT FEE.
(A) IN GENERAL. Each person that submits, on or after September 1, 2003 , an animal drug
application or a supplemental animal drug application shall be subject to a fee as follows:
(i) A fee established in subsection (b) for an animal drug application; and
(ii) A fee established in subsection (b) for a supplemental animal drug application for which
safety or effectiveness data are required, in an amount that is equal to 50 percent of the
amount of the fee under clause (i).
(B) PAYMENT. The fee required by subparagraph (A) shall be due upon submission of the
animal drug application or supplemental animal drug application.
(C) EXCEPTION FOR PREVIOUSLY FILED APPLICATION OR SUPPLEMENT. If an animal
drug application or a supplemental animal drug application was submitted by a person that
paid the fee for such application or supplement, was accepted for filing, and was not approved
or was withdrawn (without a waiver or refund), the submission of an animal drug application or
a supplemental animal drug application for the same product by the same person (or the
person’s licensee, assignee, or successor) shall not be subject to a fee under subparagraph
(A).
(D) REFUND OF FEE IF APPLICATION REFUSED FOR FILING. The Secretary shall refund
75 percent of the fee paid under subparagraph (B) for any animal drug application or
supplemental animal drug application which is refused for filing.
(E) REFUND OF FEE IF APPLICATION WITHDRAWN. If an animal drug application or a
supplemental animal drug application is withdrawn after the application or supplement was
filed, the Secretary may refund the fee or portion of the fee paid under subparagraph (B) if no
substantial work was performed on the application or supplement after the application or
supplement was filed. The Secretary shall have the sole discretion to refund the fee under this
paragraph. A determination by the Secretary concerning a refund under this paragraph shall
not be reviewable.
(2) ANIMAL DRUG PRODUCT FEE. Each person
(A) who is named as the applicant in an animal drug application or supplemental animal drug
application for an animal drug product which has been submitted for listing under section 510,
and
(B) who, after September 1, 2003 , had pending before the Secretary an animal drug
application or supplemental animal drug application; shall pay for each such animal drug
product the annual fee established in subsection (b). Such fee shall be payable for the fiscal
year in which the animal drug product is first submitted for listing under section 510, or is
submitted for relisting under section 510 if the animal drug product has been withdrawn from
listing and relisted. After such fee is paid for that fiscal year, such fee shall be payable on or
before January 31 of each year. Such fee shall be paid only once for each animal drug product
for a fiscal year in which the fee is payable.
(3) ANIMAL DRUG ESTABLISHMENT FEE. Each person
(A) who owns or operates, directly or through an affiliate, an animal drug establishment, and
(B) who is named as the applicant in an animal drug application or supplemental animal drug
application for an animal drug product which has been submitted for listing under section 510,
and
(C) who, after September 1, 2003, had pending before the Secretary an animal drug
application or supplemental animal drug application, shall be assessed an annual fee
established in subsection (b) for each animal drug establishment listed in its approved animal
drug application as an establishment that manufactures the animal drug product named in the
application. The annual establishment fee shall be assessed in each fiscal year in which the
animal drug product named in the application is assessed a fee under paragraph (2) unless
the animal drug establishment listed in the application does not engage in the manufacture of
the animal drug product during the fiscal year. The fee shall be paid on or before January 31 of
each year. The establishment shall be assessed only one fee per fiscal year under this section:
Provided, however, That where a single establishment manufactures both animal drug
products and prescription drug products, as defined in section 735(3), such establishment
shall be assessed both the animal drug establishment fee and the prescription drug
establishment fee, as set forth in section 736(a)(2), within a single fiscal year.
(4) ANIMAL DRUG SPONSOR FEE. Each person
(A) who meets the definition of an animal drug sponsor within a fiscal year; and
(B) who, after September 1, 2003 , had pending before the Secretary an animal drug
application, a supplemental animal drug application, or an investigational animal drug
submission, shall be assessed an annual fee established under subsection (b). The fee shall
be paid on or before January 31 of each year. Each animal drug sponsor shall pay only one
such fee each fiscal year.
(b) FEE AMOUNTS. Except as provided in subsection (a)(1) and subsections (c), (d), (f), and
(g), the fees required under subsection (a) shall be established to generate fee revenue
amounts as follows:
(1) TOTAL FEE REVENUES FOR APPLICATION AND SUPPLEMENT FEES. The total fee
revenues to be collected in animal drug application fees under subsection (a)(1)(A)(i) and
supplemental animal drug application fees under subsection (a)(1)(A)(ii) shall be $1,250,000 in
fiscal year 2004, $2,000,000 in fiscal year 2005, and $2,500,000 in fiscal years 2006, 2007,
and 2008.
(2) TOTAL FEE REVENUES FOR PRODUCT FEES. The total fee revenues to be collected in
product fees under subsection (a)(2) shall be $1,250,000 in fiscal year 2004, $2,000,000 in
fiscal year 2005, and $2,500,000 in fiscal years 2006, 2007, and 2008. PUBL130
(3) TOTAL FEE REVENUES FOR ESTABLISHMENT FEES. The total fee revenues to be
collected in establishment fees under subsection (a)(3) shall be $1,250,000 in fiscal year 2004,
$2,000,000 in fiscal year 2005, and $2,500,000 in fiscal years 2006, 2007, and 2008.
(4) TOTAL FEE REVENUES FOR SPONSOR FEES. The total fee revenues to be collected in
sponsor fees under subsection(a)(4) shall be $1,250,000 in fiscal year 2004, $2,000,000 in
fiscal year 2005, and $2,500,000 in fiscal years 2006, 2007, and 2008.
(c) ADJUSTMENTS.
(1) INFLATION ADJUSTMENT. The revenues established in subsection (b) shall be adjusted
by the Secretary by notice, published in the Federal Register, for a fiscal year to reflect the
greater of
(A) the total percentage change that occurred in the Consumer Price Index for all urban
consumers (all items; United States city average) for the 12-month period ending June 30
preceding the fiscal year for which fees are being established; or
(B) the total percentage change for the previous fiscal year in basic pay under the General
Schedule in accordance with section 5332 of title 5, United States Code, as adjusted by any
locality-based comparability payment pursuant to section 5304 of such title for Federal
employees stationed in the District of Columbia. The adjustment made each fiscal year by this
subsection will be added on a compounded basis to the sum of all adjustments made each
fiscal year after fiscal year 2004 under this subsection.
(2) WORKLOAD ADJUSTMENT. After the fee revenues are adjusted for inflation in
accordance with paragraph (1), the fee revenues shall be further adjusted each fiscal year
after fiscal year 2004 to reflect changes in review workload. With respect to such adjustment:
(A) This adjustment shall be determined by the Secretary based on a weighted average of the
change in the total number of animal drug applications, supplemental animal drug applications
for which data with respect to safety or effectiveness are required, manufacturing
supplemental animal drug applications, investigational animal drug study submissions, and
investigational animal drug protocol submissions submitted to the Secretary. The Secretary
shall publish in the Federal Register the fees resulting from this adjustment and the supporting
methodologies.
(B) Under no circumstances shall this workload adjustment result in fee revenues for a fiscal
year that are less than the fee revenues for that fiscal year established in subsection (b), as
adjusted for inflation under paragraph (1).
(3) FINAL YEAR ADJUSTMENT. For fiscal year 2008, the Secretary may further increase the
fees to provide for up to 3 months of operating reserves of carryover user fees for the process
for the review of animal drug applications for the first 3 months of fiscal year 2009. If the Food
and Drug Administration has carryover balances for the process for the review of animal drug
applications in excess of 3 months of such operating reserves, then this adjustment will not be
made. If this adjustment is necessary, then the rationale for the amount of the increase shall
be contained in the annual notice setting fees for fiscal year 2008.
(4) ANNUAL FEE SETTING. The Secretary shall establish, 60 days before the start of each
fiscal year beginning after September 30, 2003, for that fiscal year, animal drug application
fees, supplemental animal drug application fees, animal drug sponsor fees, animal drug
establishment fees, and animal drug product fees based on the revenue amounts established
under subsection (b) and the adjustments provided under this subsection.
(5) LIMIT. The total amount of fees charged, as adjusted under this subsection, for a fiscal
year may not exceed the total costs for such fiscal year for the resources allocated for the
process for the review of animal drug applications.
(d) FEE WAIVER OR REDUCTION.
(1) IN GENERAL. The Secretary shall grant a waiver from or a reduction of 1 or more fees
assessed under subsection (a) where the Secretary finds that
(A) the assessment of the fee would present a significant barrier to innovation because of
limited resources available to such person or other circumstances,
(B) the fees to be paid by such person will exceed the anticipated present and future costs
incurred by the Secretary in conducting the process for the review of animal drug applications
for such person,
(C) the animal drug application or supplemental animal drug application is intended solely to
provide for use of the animal drug in
(i) a Type B medicated feed (as defined in section 558.3(b)(3) of title 21, Code of Federal
Regulations (or any successor regulation)) intended for use in the manufacture of Type C
free-choice medicated feeds, or
(ii) a Type C free-choice medicated feed (as defined in section 558.3(b)(4) of title 21, Code of
Federal Regulations (or any successor regulation)),
(D) the animal drug application or supplemental animal drug application is intended solely to
provide for a minor use or minor species indication, or
(E) the sponsor involved is a small business submitting its first animal drug application to the
Secretary for review.
(2) USE OF STANDARD COSTS. In making the finding in paragraph (1)(B), the Secretary may
use standard costs.
(3) RULES FOR SMALL BUSINESSES.
(A) DEFINITION. In paragraph (1)(E), the term ‘small business’ means an entity that has fewer
than 500 employees, including employees of affiliates.
(B) WAIVER OF APPLICATION FEE. The Secretary shall waive under paragraph (1)(E) the
application fee for the first animal drug application that a small business or its affiliate submits
to the Secretary for review. After a small business or its affiliate is granted such a waiver, the
small business or its affiliate shall pay application fees for all subsequent animal drug
applications and supplemental animal drug applications for which safety or effectiveness data
are required in the same manner as an entity that does not qualify as a small business.
(C) CERTIFICATION. The Secretary shall require any person who applies for a waiver under
paragraph (1)(E) to certify their qualification for the waiver. The Secretary shall periodically
publish in the Federal Register a list of persons making such certifications.
(e) EFFECT OF FAILURE TO PAY FEES. An animal drug application or supplemental animal
drug application submitted by a person subject to fees under subsection (a) shall be
considered incomplete and shall not be accepted for filing by the Secretary until all fees owed
by such person have been paid. An investigational animal drug submission under section
739(5)(B) that is submitted by a person subject to fees under subsection (a) shall be
considered incomplete and shall not be accepted for review by the Secretary until all fees
owed by such person have been paid. The Secretary may discontinue review of any animal
drug application, supplemental animal drug application or investigational animal drug
submission from a person if such person has not submitted for payment all fees owed under
this section by 30 days after the date upon which they are due.
(f) ASSESSMENT OF FEES.
(1) LIMITATION. Fees may not be assessed under subsection (a) for a fiscal year beginning
after fiscal year 2003unless appropriations for salaries and expenses of the Food and Drug
Administration for such fiscal year (excluding the amount of fees appropriated for such fiscal
year) are equal to or greater than the amount of appropriations for the salaries and expenses
of the Food and Drug Administration for the fiscal year 2003 (excluding the amount of fees
appropriated for such fiscal year) multiplied by the adjustment factor applicable to the fiscal
year involved.
(2) AUTHORITY. If the Secretary does not assess fees under subsection (a) during any
portion of a fiscal year because of paragraph (1) and if at a later date in such fiscal year the
Secretary may assess such fees, the Secretary may assess and collect such fees, without any
modification in the rate, for animal drug applications, supplemental animal drug applications,
investigational animal drug submissions, animal drug sponsors, animal drug establishments
and animal drug products at any time in such fiscal year notwithstanding the provisions of
subsection (a) relating to the date fees are to be paid.
(g) CREDITING AND AVAILABILITY OF FEES.
(1) IN GENERAL. Fees authorized under subsection (a) shall be collected and available for
obligation only to the extent and in the amount provided in advance in appropriations Acts.
Such fees are authorized to be appropriated to remain available until expended. Such sums as
may be necessary may be transferred from the Food and Drug Administration salaries and
expenses appropriation account without fiscal year limitation to such appropriation account for
salary and expenses with such fiscal year limitation. The sums transferred shall be available
solely for the process for the review of animal drug applications.
(2) COLLECTIONS AND APPROPRIATION ACTS.
(A) IN GENERAL. The fees authorized by this section
(i) shall be retained in each fiscal year in an amount not to exceed the amount specified in
appropriation Acts, or otherwise made available for obligation for such fiscal year, and
(ii) shall only be collected and available to defray increases in the costs of the resources
allocated for the process for the review of animal drug applications (including increases in such
costs for an additional number of full-time equivalent positions in the Department of Health and
Human Services to be engaged in such process) over such costs, excluding costs paid from
fees collected under this section, for fiscal year 2003 multiplied by the adjustment factor.
(B) COMPLIANCE. The Secretary shall be considered to have met the requirements of
subparagraph (A)(ii) in any fiscal year if the costs funded by appropriations and allocated for
the process for the review of animal drug applications
(i) are not more than 3 percent below the level specified in subparagraph (A)(ii); or
(ii)(I) are more than 3 percent below the level specified in subparagraph (A)(ii), and fees
assessed for the fiscal year following the subsequent fiscal year are decreased by the amount
in excess of 3 percent by which such costs fell below the level specified in subparagraph (A)(ii);
and
(II) such costs are not more than 5 percent below the level specified in subparagraph (A)(ii).
(3) AUTHORIZATION OF APPROPRIATIONS. There are authorized to be appropriated for
fees under this section
(A) $5,000,000 for fiscal year 2004;
(B) $8,000,000 for fiscal year 2005;
(C) $10,000,000 for fiscal year 2006;
(D) $10,000,000 for fiscal year 2007; and
(E) $10,000,000 for fiscal year 2008; as adjusted to reflect adjustments in the total fee
revenues made under this section and changes in the total amounts collected by animal drug
application fees, supplemental animal drug application fees, animal drug sponsor fees, animal
drug establishment fees, and animal drug product fees.
(4) OFFSET. Any amount of fees collected for a fiscal year under this section that exceeds the
amount of fees specified in appropriations Acts for such fiscal year shall be credited to the
appropriation account of the Food and Drug Administration as provided in paragraph (1), and
shall be subtracted from the amount of fees that would otherwise be authorized to be collected
under this section pursuant to appropriation Acts for a subsequent fiscal year.
(h) COLLECTION OF UNPAID FEES. In any case where the Secretary does not receive
payment of a fee assessed under subsection (a) within 30 days after it is due, such fee shall be
treated as a claim of the United States Government subject to subchapter II of chapter 37 of
title 31, United States Code.
(i) WRITTEN REQUESTS FOR WAIVERS, REDUCTIONS, AND REFUNDS. To qualify for
consideration for a waiver or reduction under subsection (d), or for a refund of any fee
collected in accordance with subsection (a), a person shall submit to the Secretary a written
request for such waiver, reduction, or refund not later than 180 days after such fee is due.
(j) CONSTRUCTION. This section may not be construed to require that the number of full-time
equivalent positions in the Department of Health and Human Services, for officers, employees,
and advisory committees not engaged in the process of the review of animal drug applications,
be reduced to offset the number of officers, employees, and advisory committees so engaged.
(k) ABBREVIATED NEW ANIMAL DRUG APPLICATIONS. The Secretary shall
(1) to the extent practicable, segregate the review of abbreviated new animal drug applications
from the process for the review of animal drug applications, and
(2) adopt other administrative procedures to ensure that review times of abbreviated new
animal drug applications do not increase from their current level due to activities under the
user fee program.
Footnotes: Chapter VII, Subchapter C
1. Sections 503 and 504 of Public Law 107–188 (116 Stat. 688, 689) amended sections 735
and 736, respectively. Section 509 of such Public Law provides as follows:
SEC. 509. SUNSET CLAUSE.
The amendments made by sections 503 and 504 cease to be effective October 1, 2007, and
section 505 ceases to be effective 120 days after such date.
2. See footnote for the beginning of section 735.
3. Section 507 was repealed by section 125(b)(1) of Public Law 105–115 (111 Stat. 2325).
4. Subtitle A of title V of Public Law 107–188, which was enacted June 12, 2002.
5. The amendment described in section 504(f)(1) of Public Law 107–188 (116 Stat. 691)
cannot be executed. The amendment includes language to strike "Fees collected for a fiscal
year" and all that follows through "fiscal year limitation.". The latter term appears at the end of
the first sentence and at the end of the second sentence, but the amendatory instructions do
not identify to which instance of the use of such term the amendment applies.
The probable intent of the Congress is that the second sentence remain in effect, since section
738(h)(1) of this Act, which relates to the crediting and availability of device fees, has language
substantially similar to the second sentence and was added after the enactment of Public Law
107–188. (Section 738 was added by section 102 of Public Law 107–250, enacted October 26,
2002. Public Law 107–188 was enacted June 12, 2002.) Section 504(f)(1) of Public Law
107–188 provides as follows:
"(1) IN GENERAL. Section 736(g)(1) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C.
379h(g)(1)) is amended by striking 'Fees collected for a fiscal year' and all that follows through
'fiscal year limitation.' and inserting the following: 'Fees authorized under subsection (a) shall
be collected and available for obligation only to the extent and in the amount provided in
advance in appropriations Acts. Such fees are authorized to remain available until expended.'
".
6. Part 3 was added by title I of Public Law 107–250 (116 Stat. 1589). See section 102 of that
title. Section 107 of that title provides as follows:
SEC. 107. SUNSET CLAUSE.
The amendments made by this title cease to be effective October 1, 2007, except that section
103 with respect to annual reports ceases to be effective January 31, 2008.
7. See footnote for the beginning of section 737.
8. Public Law 107–250, enacted October 26, 2002.
9. See footnote for pargraph (1).
CHAPTER VII—GENERAL AUTHORITY SUBCHAPTER D--INFORMATION AND EDUCATION
SEC. 741. [ 21 U.S.C. 379k] INFORMATION SYSTEM.
The Secretary shall establish and maintain an information system to track the status and
progress of each application or submission (including a petition, notification, or other similar
form of request) submitted to the Food and Drug Administration requesting agency action.
SEC. 742. [ 21 U.S.C. 379l] EDUCATION.
(a) IN GENERAL.—The Secretary shall conduct training and education programs for the
employees of the Food and Drug Administration relating to the regulatory responsibilities and
policies established by this Act, including programs for—
(1) scientific training;
(2) training to improve the skill of officers and employees authorized to conduct inspections
under section 704;
(3) training to achieve product specialization in such inspections; and
(4) training in administrative process and procedure and integrity issues.
(b) INTRAMURAL FELLOWSHIPS AND OTHER TRAINING PROGRAMS.— The Secretary,
acting through the Commissioner, may, through fellowships and other training programs,
conduct and support intramural research training for predoctoral and postdoctoral scientists
and physicians.
CHAPTER VII—GENERAL AUTHORITY SUBCHAPTER E--ENVIRONMENTAL IMPACT REVIEW
SEC. 746. [ 21 U.S.C. 379o] ENVIRONMENTAL IMPACT.
Notwithstanding any other provision of law, an environmental impact statement prepared in
accordance with the regulations published in part 25 of title 21, Code of Federal Regulations
(as in effect on August 31, 1997) in connection with an action carried out under (or a
recommendation or report relating to) this Act, shall be considered to meet the requirements
for a detailed statement under section 102(2)(C) of the National Environmental Policy Act of
1969 (42 U.S.C. 4332(2)(C)).
CHAPTER VII—GENERAL AUTHORITY SUBCHAPTER F--NATIONAL UNIFORMITY FOR NONPRESCRIPTION DRUGS
AND PREEMPTION FOR LABELING OR PACKAGING OF COSMETICS
SEC. 751. [ 21 U.S.C. 379r] NATIONAL UNIFORMITY FOR NONPRESCRIPTION DRUGS.
(a) IN GENERAL.—Except as provided in subsection (b), (c)(1), (d), (e), or (f), no State or
political subdivision of a State may establish or continue in effect any requirement—
(1) that relates to the regulation of a drug that is not subject to the requirements of section
503(b)(1) or 503(f)(1)(A); and
(2) that is different from or in addition to, or that is otherwise not identical with, a requirement
under this Act, the Poison Prevention Packaging Act of 1970 (15 U.S.C. 1471 et seq.), or the
Fair Packaging and Labeling Act (15 U.S.C. 1451 et seq.).
(b) EXEMPTION.—
(1) IN GENERAL.—Upon application of a State or political subdivision thereof, the Secretary
may by regulation, after notice and opportunity for written and oral presentation of views,
exempt from subsection (a), under such conditions as may be prescribed in such regulation, a
State or political subdivision requirement that—
(A) protects an important public interest that would otherwise be unprotected, including the
health and safety of children;
(B) would not cause any drug to be in violation of any applicable requirement or prohibition
under Federal law; and
(C) would not unduly burden interstate commerce.
(2) TIMELY ACTION.—The Secretary shall make a decision on the exemption of a State or
political subdivision requirement under paragraph (1) not later than 120 days after receiving
the application of the State or political subdivision under paragraph(1).
(c) SCOPE.—
(1) IN GENERAL.—This section shall not apply to—
(A) any State or political subdivision requirement that relates to the practice of pharmacy; or
(B) any State or political subdivision requirement that a drug be dispensed only upon the
prescription of a practitioner licensed by law to administer such drug.
(2) SAFETY OR EFFECTIVENESS.—For purposes of subsection (a), a requirement that
relates to the regulation of a drug shall be deemed to include any requirement relating to public
information or any other form of public communication relating to a warning of any kind for a
drug.
(d) EXCEPTIONS.—
(1) IN GENERAL.—In the case of a drug described in subsection (a)(1) that is not the subject
of an application approved under section 505 or section 507 (as in effect on the day before the
date of enactment of the Food and Drug Administration Modernization Act of 1997) or a final
regulation promulgated by the Secretary establishing conditions under which the drug is
generally recognized as safe and effective and not misbranded, subsection (a) shall apply only
with respect to a requirement of a State or political subdivision of a State that relates to the
same subject as, but is different from or in addition to, or that is otherwise not identical with—
(A) a regulation in effect with respect to the drug pursuant to a statute described in subsection
(a)(2); or
(B) any other requirement in effect with respect to the drug pursuant to an amendment to such
a statute made on or after the date of enactment of the Food and Drug Administration
Modernization Act of 1997.
(2) STATE INITIATIVES.—This section shall not apply to a State requirement adopted by a
State public initiative or referendum enacted prior to September 1, 1997 .
(e) NO EFFECT ON PRODUCT LIABILITY LAW.—Nothing in this section shall be construed
to modify or otherwise affect any action or the liability of any person under the product liability
law of any State.
(f) STATE ENFORCEMENT AUTHORITY.—Nothing in this section shall prevent a State or
political subdivision thereof from enforcing, under any relevant civil or other enforcement
authority, a requirement that is identical to a requirement of this Act.
SEC. 752. [ 21 U.S.C. 379s] PREEMPTION FOR LABELING OR PACKAGING OF
COSMETICS.
(a) IN GENERAL.—Except as provided in subsection (b), (d), or (e), no State or political
subdivision of a State may establish or continue in effect any requirement for labeling or
packaging of a cosmetic that is different from or in addition to, or that is otherwise not identical
with, a requirement specifically applicable to a particular cosmetic or class of cosmetics under
this Act, the Poison Prevention Packaging Act of 1970 (15 U.S.C. 1471 et seq.), or the Fair
Packaging and Labeling Act (15 U.S.C. 1451 et seq.).
(b) EXEMPTION.—Upon application of a State or political subdivision thereof, the Secretary
may by regulation, after notice and opportunity for written and oral presentation of views,
exempt from subsection (a), under such conditions as may be prescribed in such regulation, a
State or political subdivision requirement for labeling or packaging that—
(1) protects an important public interest that would otherwise be unprotected;
(2) would not cause a cosmetic to be in violation of any applicable requirement or prohibition
under Federal law; and
(3) would not unduly burden interstate commerce.
(c) SCOPE.—For purposes of subsection (a), a reference to a State requirement that relates to
the packaging or labeling of a cosmetic means any specific requirement relating to the same
aspect of such cosmetic as a requirement specifically applicable to that particular cosmetic or
class of cosmetics under this Act for packaging or labeling, including any State requirement
relating to public information or any other form of public communication.
(d) NO EFFECT ON PRODUCT LIABILITY LAW.—Nothing in this section shall be construed
to modify or otherwise affect any action or the liability of any person under the product liability
law of any State.
(e) STATE INITIATIVE.—This section shall not apply to a State requirement adopted by a
State public initiative or referendum enacted prior to September 1, 1997.
CHAPTER VII—GENERAL AUTHORITY SUBCHAPTER G--SAFETY REPORTS
SEC. 756. [ 21 U.S.C. 379v] SAFETY REPORT DISCLAIMERS.
With respect to any entity that submits or is required to submit a safety report or other
information in connection with the safety of a product (including a product that is a food, drug,
device, dietary supplement, or cosmetic) under this Act (and any release by the Secretary of
that report or information), such report or information shall not be construed to reflect
necessarily a conclusion by the entity or the Secretary that the report or information constitutes
an admission that the product involved malfunctioned, caused or contributed to an adverse
experience, or otherwise caused or contributed to a death, serious injury, or serious illness.
Such an entity need not admit, and may deny, that the report or information submitted by the
entity constitutes an admission that the product involved malfunctioned, caused or contributed
to an adverse experience, or caused or contributed to a death, serious injury, or serious
illness.
SEC. 760 [21 USC § 379aa] SERIOUS ADVERSE EVENT REPORTING FOR
NONPRESCRIPTION DRUGS [Caution: This section is effective 1 year after enactment,
pursuant to § 2(e)(1) of Act Dec. 22, 2006, P.L. 109-462]
(a) Definitions. In this section:
(1) Adverse event. The term "adverse event" means any health-related event associated with
the use of a nonprescription drug that is adverse, including--
(A) an event occurring from an overdose of the drug, whether accidental or intentional;
(B) an event occurring from abuse of the drug;
(C) an event occurring from withdrawal from the drug; and
(D) any failure of expected pharmacological action of the drug.
(2) Nonprescription drug. The term "nonprescription drug" means a drug that is--
(A) not subject to section 503(b) [21 USC § 353(b)]; and
(B) not subject to approval in an application submitted under section 505 [21 USC § 355].
(3) Serious adverse event. The term "serious adverse event" is an adverse event that--
(A) results in--
(i) death;
(ii) a life-threatening experience;
(iii) inpatient hospitalization;
(iv) a persistent or significant disability or incapacity; or
(v) a congenital anomaly or birth defect; or
(B) requires, based on reasonable medical judgment, a medical or surgical intervention to
prevent an outcome described under subparagraph (A).
(4) Serious adverse event report. The term "serious adverse event report" means a report that
is required to be submitted to the Secretary under subsection (b).
(b) Reporting requirement.
(1) In general. The manufacturer, packer, or distributor whose name (pursuant to section
502(b)(1) [21 USC § 352(b)(1)]) appears on the label of a nonprescription drug marketed in the
United States (referred to in this section as the "responsible person") shall submit to the
Secretary any report received of a serious adverse event associated with such drug when
used in the United States, accompanied by a copy of the label on or within the retail package
of such drug.
(2) Retailer. A retailer whose name appears on the label described in paragraph (1) as a
distributor may, by agreement, authorize the manufacturer or packer of the nonprescription
drug to submit the required reports for such drugs to the Secretary so long as the retailer
directs to the manufacturer or packer all adverse events associated with such drug that are
reported to the retailer through the address or telephone number described in section 502(x)
[21 USC § 352(x)].
(c) Submission of reports.
(1) Timing of reports. The responsible person shall submit to the Secretary a serious adverse
event report no later than 15 business days after the report is received through the address or
phone number described in section 502(x) [21 USC § 352(x)].
(2) New medical information. The responsible person shall submit to the Secretary any new
medical information, related to a submitted serious adverse event report that is received by the
responsible person within 1 year of the initial report, no later than 15 business days after the
new information is received by the responsible person.
(3) Consolidation of reports. The Secretary shall develop systems to ensure that duplicate
reports of, and new medical information related to, a serious adverse event shall be
consolidated into a single report.
(4) Exemption. The Secretary, after providing notice and an opportunity for comment from
interested parties, may establish an exemption to the requirements under paragraphs (1) and
(2) if the Secretary determines that such exemption would have no adverse effect on public
health.
(d) Contents of reports. Each serious adverse event report under this section shall be
submitted to the Secretary using the MedWatch form, which may be modified by the Secretary
for nonprescription drugs, and may be accompanied by additional information.
(e) Maintenance and inspection of records.
(1) Maintenance. The responsible person shall maintain records related to each report of an
adverse event received by the responsible person for a period of 6 years.
(2) Records inspection.
(A) In general. The responsible person shall permit an authorized person to have access to
records required to be maintained under this section, during an inspection pursuant to section
704 [21 USC § 374].
(B) Authorized person. For purposes of this paragraph, the term "authorized person" means an
officer or employee of the Department of Health and Human Services who has--
(i) appropriate credentials, as determined by the Secretary; and
(ii) been duly designated by the Secretary to have access to the records required under this
section.
(f) Protected information. A serious adverse event report submitted to the Secretary under this
section, including any new medical information submitted under subsection (c)(2), or an
adverse event report voluntarily submitted to the Secretary shall be considered to be--
(1) a safety report under section 756 [21 USC § 379v] and may be accompanied by a
statement, which shall be a part of any report that is released for public disclosure, that denies
that the report or the records constitute an admission that the product involved caused or
contributed to the adverse event; and
(2) a record about an individual under section 552a of title 5, United States Code [5 USC §
552a] (commonly referred to as the "Privacy Act of 1974") and a medical or similar file the
disclosure of which would constitute a violation of section 552 of such title 5 [5 USC § 552]
(commonly referred to as the "Freedom of Information Act"), and shall not be publicly disclosed
unless all personally identifiable information is redacted.
(g) Rule of construction. The submission of any adverse event report in compliance with this
section shall not be construed as an admission that the nonprescription drug involved caused
or contributed to the adverse event.
(h) Preemption.
(1) In general. No State or local government shall establish or continue in effect any law,
regulation, order, or other requirement, related to a mandatory system for adverse event
reports for nonprescription drugs, that is different from, in addition to, or otherwise not identical
to, this section.
(2) Effect of section.
(A) In general. Nothing in this section shall affect the authority of the Secretary to provide
adverse event reports and information to any health, food, or drug officer or employee of any
State, territory, or political subdivision of a State or territory, under a memorandum of
understanding between the Secretary and such State, territory, or political subdivision.
(B) Personally-identifiable information. Notwithstanding any other provision of law,
personally-identifiable information in adverse event reports provided by the Secretary to any
health, food, or drug officer or employee of any State, territory, or political subdivision of a
State or territory, shall not--
(i) be made publicly available pursuant to any State or other law requiring disclosure of
information or records; or
(ii) otherwise be disclosed or distributed to any party without the written consent of the
Secretary and the person submitting such information to the Secretary.
(C) Use of safety reports. Nothing in this section shall permit a State, territory, or political
subdivision of a State or territory, to use any safety report received from the Secretary in a
manner inconsistent with subsection (g) or section 756 [21 USC § 379v].
(i) Authorization of appropriations. There are authorized to be appropriated to carry out this
section such sums as may be necessary.
SEC. 761. [21 USC § 379aa-1] SERIOUS ADVERSE EVENT REPORTING FOR DIETARY
SUPPLEMENTS [Caution: This section is effective 1 year after enactment, pursuant to §
3(d)(1) of Act Dec. 22, 2006, P.L. 109-462]
(a) Definitions. In this section:
(1) Adverse event. The term "adverse event" means any health-related event associated with
the use of a dietary supplement that is adverse.
(2) Serious adverse event. The term "serious adverse event" is an adverse event that--
(A) results in--
(i) death;
(ii) a life-threatening experience;
(iii) inpatient hospitalization;
(iv) a persistent or significant disability or incapacity; or
(v) a congenital anomaly or birth defect; or
(B) requires, based on reasonable medical judgment, a medical or surgical intervention to
prevent an outcome described under subparagraph (A).
(3) Serious adverse event report. The term "serious adverse event report" means a report that
is required to be submitted to the Secretary under subsection (b).
(b) Reporting requirement.
(1) In general. The manufacturer, packer, or distributor of a dietary supplement whose name
(pursuant to section 403(e)(1) [21 USC § 343(e)(1)]) appears on the label of a dietary
supplement marketed in the United States (referred to in this section as the "responsible
person") shall submit to the Secretary any report received of a serious adverse event
associated with such dietary supplement when used in the United States, accompanied by a
copy of the label on or within the retail packaging of such dietary supplement.
(2) Retailer. A retailer whose name appears on the label described in paragraph (1) as a
distributor may, by agreement, authorize the manufacturer or packer of the dietary supplement
to submit the required reports for such dietary supplements to the Secretary so long as the
retailer directs to the manufacturer or packer all adverse events associated with such dietary
supplement that are reported to the retailer through the address or telephone number
described in section 403(y) [21 USC § 343(y)].
(c) Submission of reports.
(1) Timing of reports. The responsible person shall submit to the Secretary a serious adverse
event report no later than 15 business days after the report is received through the address or
phone number described in section 403(y) [21 USC § 343(y)].
(2) New medical information. The responsible person shall submit to the Secretary any new
medical information, related to a submitted serious adverse event report that is received by the
responsible person within 1 year of the initial report, no later than 15 business days after the
new information is received by the responsible person.
(3) Consolidation of reports. The Secretary shall develop systems to ensure that duplicate
reports of, and new medical information related to, a serious adverse event shall be
consolidated into a single report.
(4) Exemption. The Secretary, after providing notice and an opportunity for comment from
interested parties, may establish an exemption to the requirements under paragraphs (1) and
(2) if the Secretary determines that such exemption would have no adverse effect on public
health.
(d) Contents of reports. Each serious adverse event report under this section shall be
submitted to the Secretary using the MedWatch form, which may be modified by the Secretary
for dietary supplements, and may be accompanied by additional information.
(e) Maintenance and inspection of records.
(1) Maintenance. The responsible person shall maintain records related to each report of an
adverse event received by the responsible person for a period of 6 years.
(2) Records inspection.
(A) In general. The responsible person shall permit an authorized person to have access to
records required to be maintained under this section during an inspection pursuant to section
704 [21 USC § 374].
(B) Authorized person. For purposes of this paragraph, the term "authorized person" means
an officer or employee of the Department of Health and Human Services, who has—
(i) appropriate credentials, as determined by the Secretary; and
(ii) been duly designated by the Secretary to have access to the records required under this
section.
(f) Protected information. A serious adverse event report submitted to the Secretary under this
section, including any new medical information submitted under subsection (c)(2), or an
adverse event report voluntarily submitted to the Secretary shall be considered to be--
(1) a safety report under section 756 [21 USC § 379v] and may be accompanied by a
statement, which shall be a part of any report that is released for public disclosure, that denies
that the report or the records constitute an admission that the product involved caused or
contributed to the adverse event; and
(2) a record about an individual under section 552a of title 5, United States Code [5 USC §
552a] (commonly referred to as the "Privacy Act of 1974") and a medical or similar file the
disclosure of which would constitute a violation of section 552 of such title 5 [5 USC § 552]
(commonly referred to as the "Freedom of Information Act"), and shall not be publicly disclosed
unless all personally identifiable information is redacted.
(g) Rule of construction. The submission of any adverse event report in compliance with this
section shall not be construed as an admission that the dietary supplement involved caused or
contributed to the adverse event.
(h) Preemption.
(1) In general. No State or local government shall establish or continue in effect any law,
regulation, order, or other requirement, related to a mandatory system for adverse event
reports for dietary supplements, that is different from, in addition to, or otherwise not identical
to, this section.
(2) Effect of section.
(A) In general. Nothing in this section shall affect the authority of the Secretary to provide
adverse event reports and information to any health, food, or drug officer or employee of any
State, territory, or political subdivision of a State or territory, under a memorandum of
understanding between the Secretary and such State, territory, or political subdivision.
(B) Personally-identifiable information. Notwithstanding any other provision of law,
personally-identifiable information in adverse event reports provided by the Secretary to any
health, food, or drug officer or employee of any State, territory, or political subdivision of a
State or territory, shall not--
(i) be made publicly available pursuant to any State or other law requiring disclosure of
information or records; or
(ii) otherwise be disclosed or distributed to any party without the written consent of the
Secretary and the person submitting such information to the Secretary.
(C) Use of safety reports. Nothing in this section shall permit a State, territory, or political
subdivision of a State or territory, to use any safety report received from the Secretary in a
manner inconsistent with subsection (g) or section 756 [21 USC § 379v].
(i) Authorization of appropriations. There are authorized to be appropriated to carry out this
section such sums as may be necessary.
CHAPTER VIII—IMPORTS AND EXPORTS
IMPORTS AND EXPORTS
SEC. 801. [21 USC 381] Imports and exports [Caution: See prospective amendment note
below.]
(a) Imports; list of registered foreign establishments; samples from unregistered foreign
establishments; examination and refusal of admission. The Secretary of the Treasury shall
deliver to the Secretary of Health and Human Services, upon his request, samples of food,
drugs, devices, and cosmetics which are being imported or offered for import into the United
States, giving notice thereof to the owner or consignee, who may appear before the Secretary
of Health and Human Services and have the right to introduce testimony. The Secretary of
Health and Human Services shall furnish to the Secretary of the Treasury a list of
establishments registered pursuant to subsection (i) of section 510 and shall request that if any
drugs or devices manufactured, prepared, propagated, compounded, or processed in an
establishment not so registered are imported or offered for import into the United States,
samples of such drugs or devices be delivered to the Secretary of Health and Human Services,
with notice of such delivery to the owner or consignee, who may appear before the Secretary
of Health and Human Services and have the right to introduce testimony. If it appears from the
examination of such samples or otherwise that (1) such article has been manufactured,
processed, or packed under insanitary conditions or, in the case of a device, the methods used
in, or the facilities or controls used for, the manufacture, packing, storage, or installation of the
device do not conform to the requirements of section 520(f), or (2) such article is forbidden or
restricted in sale in the country in which it was produced or from which it was exported, or (3)
such article is adulterated, misbranded, or in violation of section 505, then such article shall be
refused admission, except as provided in subsection (b) of this section. The Secretary of the
Treasury shall cause the destruction of any such article refused admission unless such article
is exported, under regulations prescribed by the Secretary of the Treasury, within ninety days
of the date of notice of such refusal or within such additional time as may be permitted
pursuant to such regulations. Clause (2) of the third sentence of this paragraph 1 [subsection]
shall not be construed to prohibit the admission of narcotic drugs the importation of which is
permitted under the Controlled Substances Import and Export Act.
(b) Disposition of refused articles. Pending decision as to the admission of an article being
imported or offered for import, the Secretary of the Treasury may authorize delivery of such
article to the owner or consignee upon the execution by him of a good and sufficient bond
providing for the payment of such liquidated damages in the event of default as may be
required pursuant to regulations of the Secretary of the Treasury. If it appears to the Secretary
of Health and Human Services that an article included within the provisions of clause (3) of
subsection (a) of this section can, by relabeling or other action, be brought into compliance
with the Act or rendered other than a food, drug, device, or cosmetic, final determination as to
admission of such article may be deferred and, upon filing of timely written application by the
owner or consignee and the execution by him of a bond as provided in the preceding
provisions of this subsection, the Secretary may, in accordance with regulations, authorize the
applicant to perform such relabeling or other action specified in such authorization (including
destruction or export of rejected articles or portions thereof, as may be specified in the
Secretary's authorization). All such relabeling or other action pursuant to such authorization
shall in accordance with regulations be under the supervision of an officer or employee of the
Department of Health and Human Services designated by the Secretary, or an officer or
employee of the Department of the Treasury designated by the Secretary of the Treasury.
(c) Charges concerning refused articles. All expenses (including travel, per diem or
subsistence, and salaries of officers or employees of the United States) in connection with the
destruction provided for in subsection (a) of this section and the supervision of the relabeling
or other action authorized under the provisions of subsection (b) of this section, the amount of
such expenses to be determined in accordance with regulations, and all expenses in
connection with the storage, cartage, or labor with respect to any article refused admission
under subsection (a) of this section, shall be paid by the owner or consignee and, in default of
such payment, shall constitute a lien against any future importations made by such owner or
consignee.
(d) Reimportation.
(1) Except as provided in paragraph (2) and section 804, no drug subject to section 503(b) or
composed wholly or partly of insulin which is manufactured in a State and exported may be
imported into the United States unless the drug is imported by the manufacturer of the drug.
(2) The Secretary may authorize the importation of a drug the importation of which is
prohibited by paragraph (1) if the drug is required for emergency medical care.
(3)(A) Subject to subparagraph (B), no component of a drug, no component part or accessory
of a device, or other article of device requiring further processing, which is ready or suitable for
use for health-related purposes, and no article of a food additive, color additive, or dietary
supplement, including a product in bulk form, shall be excluded from importation into the
United States under subsection (a) if each of the following conditions is met:
(i) The importer of such article of a drug or device or importer of such article of a food additive,
color additive, or dietary supplement submits to the Secretary, at the time of initial importation,
a statement in accordance with the following:
(I) Such statement provides that such article is intended to be further processed by the initial
owner or consignee, or incorporated by the initial owner or consignee, into a drug, biological
product, device, food, food additive, color additive, or dietary supplement that will be exported
by the initial owner or consignee from the United States in accordance with subsection (e) or
section 802, or with section 351(h) of the Public Health Service Act.
(II) The statement identifies the manufacturer of such article and each processor, packer,
distributor, or other entity that had possession of the article in the chain of possession of the
article from the manufacturer to such importer of the article.
(III) The statement is accompanied by such certificates of analysis as are necessary to identify
such article, unless the article is a device or is an article described in paragraph (4).
(ii) At the time of initial importation and before the delivery of such article to the importer or the
initial owner or consignee, such owner or consignee executes a good and sufficient bond
providing for the payment of such liquidated damages in the event of default as may be
required pursuant to regulations of the Secretary of the Treasury.
(iii) Such article is used and exported by the initial owner or consignee in accordance with the
intent described under clause (i)(I), except for any portions of the article that are destroyed.
(iv) The initial owner or consignee maintains records on the use or destruction of such article
or portions thereof, as the case may be, and submits to the Secretary any such records
requested by the Secretary.
(v) Upon request of the Secretary, the initial owner or consignee submits a report that provides
an accounting of the exportation or destruction of such article or portions thereof, and the
manner in which such owner or consignee complied with the requirements of this
subparagraph.
(B) Notwithstanding subparagraph (A), the Secretary may refuse admission to an article that
otherwise would be imported into the United States under such subparagraph if the Secretary
determines that there is credible evidence or information indicating that such article is not
intended to be further processed by the initial owner or consignee, or incorporated by the initial
owner or consignee, into a drug, biological product, device, food, food additive, color additive,
or dietary supplement that will be exported by the initial owner or consignee from the United
States in accordance with subsection (e) or section 802, or with section 351(h) of the Public
Health Service Act.
(C) This section may not be construed as affecting the responsibility of the Secretary to ensure
that articles imported into the United States under authority of subparagraph (A) meet each of
the conditions established in such subparagraph for importation.''
(4) The importation into the United States of blood, blood components, source plasma, or
source leukocytes or of a component, accessory, or part thereof is not permitted pursuant to
paragraph (3) unless the importation complies with section 351(a) of the Public Health Service
Act or the Secretary permits the importation under appropriate circumstances and conditions,
as determined by the Secretary. The importation of tissue or a component or part of tissue is
not permitted pursuant to paragraph (3) unless the importation complies with section 361 of
the Public Health Service Act.
(e) Exports.
(1) A food, drug, device, or cosmetic intended for export shall not be deemed to be adulterated
or misbranded under this Act if it
(A) accords to the specifications of the foreign purchaser,
(B) is not in conflict with the laws of the country to which it is intended for export,
(C) is labeled on the outside of the shipping package that it is intended for export, and
(D) is not sold or offered for sale in domestic commerce.
(2) Paragraph (1) does not apply to any device
(A) which does not comply with an applicable requirement of section 514 or 515,
(B) which under section 520(g) is exempt from either such section, or
(C) which is a banned device under section 516,
unless, in addition to the requirements of paragraph (1), either (i) the Secretary has
determined that the exportation of the device is not contrary to public health and safety and
has the approval of the country to which it is intended for export or (ii) the device is eligible for
export under section 802.
(3) A new animal drug that requires approval under section 512 shall not be exported pursuant
to paragraph (1) if such drug has been banned in the United States.
(4)(A) Any person who exports a drug, animal drug, or device may request that the Secretary
(i) certify in writing that the exported drug, animal drug, or device meets the requirements of
paragraph (1) or section 802; or
(ii) certify in writing that the drug, animal drug, or device being exported meets the applicable
requirements of this Act upon a showing that the drug or device meets the applicable
requirements of this Act.
The Secretary shall issue such a certification within 20 days of the receipt of a request for such
certification.
(B) If the Secretary issues a written export certification within the 20 days prescribed by
subparagraph (A), a fee for such certification may be charged but shall not exceed $175 for
each certification. Fees collected for a fiscal year pursuant to this subparagraph shall be
credited to the appropriation account for salaries and expenses of the Food and Drug
Administration and shall be available in accordance with appropriations Acts until expended
without fiscal year limitation. Such fees shall be collected in each fiscal year in an amount
equal to the amount specified in appropriations Acts for such fiscal year and shall only be
collected and available for the costs of the Food and Drug Administration.
(f) Labeling of exported drugs.
(1) If a drug (other than insulin, an antibiotic drug, an animal drug, or a drug exported under
section 802) being exported in accordance with subsection (e) is being exported to a country
that has different or additional labeling requirements or conditions for use and such country
requires the drug to be labeled in accordance with those requirements or uses, such drug may
be labeled in accordance with such requirements and conditions for use in the country to
which such drug is being exported if it also is labeled in accordance with the requirements of
this Act.
(2) If, pursuant to paragraph (1), the labeling of an exported drug includes conditions for use
that have not been approved under this Act, the labeling must state that such conditions for
use have not been approved under this Act. A drug exported under section 802 is exempt from
this section.
(g) Warning notices of importation in violation of 21 USC §§ 301 et seq.
(1) With respect to a prescription drug being imported or offered for import into the United
States, the Secretary, in the case of an individual who is not in the business of such
importations, may not send a warning notice to the individual unless the following conditions
are met:
(A) The notice specifies, as applicable to the importation of the drug, that the Secretary has
made a determination that
(i) importation is in violation of section 801(a) [subsec. (a) of this section] because the drug is
or appears to be adulterated, misbranded, or in violation of section 505;
(ii) importation is in violation of section 801(a) [subsec. (a) of this section] because the drug is
or appears to be forbidden or restricted in sale in the country in which it was produced or from
which it was exported;
(iii) importation is or appears to be in violation of section 801(d)(1) [subsec. (d)(1) of this
section]; or
(iv) importation otherwise is or appears to be in violation of Federal law.
(B) The notice does not specify any provision described in subparagraph (A) that is not
applicable to the importation of the drug.
(C) The notice states the reasons underlying such determination by the Secretary, including a
brief application to the principal facts involved of the provision of law described in
subparagraph (A) that is the basis of the determination by the Secretary.
(2) For purposes of this section, the term "warning notice", with respect to the importation of a
drug, means a communication from the Secretary (written or otherwise) notifying a person, or
clearly suggesting to the person, that importing the drug for personal use is, or appears to be,
a violation of this Act.
(h) Protection against adulteration of food.
(1) 2 The Secretary shall give high priority to increasing the number of inspections under this
section for the purpose of enabling the Secretary to inspect food offered for import at ports of
entry into the United States , with the greatest priority given to inspections to detect the
intentional adulteration of food.
(2) The Secretary shall give high priority to making necessary improvements to the information
management systems of the Food and Drug Administration that contain information related to
foods imported or offered for import into the United States for purposes of improving the ability
of the Secretary to allocate resources, detect the intentional adulteration of food, and facilitate
the importation of food that is in compliance with this Act.
(3) The Secretary shall improve linkages with other regulatory agencies of the Federal
Government that share responsibility for food safety, and shall with respect to such safety
improve linkages with the States and Indian tribes (as defined in section 4(e) of the Indian
Self-Determination and Education Assistance Act (25 U.S.C. 450b(e))).
(i) Testing for rapid detection of adulteration of food.
(1) 2 For use in inspections of food under this section, the Secretary shall provide for research
on the development of tests and sampling methodologies
(A) whose purpose is to test food in order to rapidly detect the adulteration of the food, with the
greatest priority given to detect the intentional adulteration of food; and
(B) whose results offer significant improvements over the available technology in terms of
accuracy, timing, or costs.
(2) In providing for research under paragraph (1), the Secretary shall give priority to conducting
research on the development of tests that are suitable for inspections of food at ports of entry
into the United States .
(3) In providing for research under paragraph (1), the Secretary shall as appropriate
coordinate with the Director of the Centers for Disease Control and Prevention, the Director of
the National Institutes of Health, the Administrator of the Environmental Protection Agency,
and the Secretary of Agriculture.
(4) The Secretary shall annually submit to the Committee on Energy and Commerce of the
House of Representatives, and the Committee on Health, Education, Labor, and Pensions of
the Senate, a report describing the progress made in research under paragraph (1), including
progress regarding paragraph (2).
(j) Temporary holds at ports of entry.
(1) If an officer or qualified employee of the Food and Drug Administration has credible
evidence or information indicating that an article of food presents a threat of serious adverse
health consequences or death to humans or animals, and such officer or qualified employee is
unable to inspect, examine, or investigate such article upon the article being offered for import
at a port of entry into the United States, the officer or qualified employee shall request the
Secretary of Treasury to hold the food at the port of entry for a reasonable period of time, not
to exceed 24 hours, for the purpose of enabling the Secretary to inspect, examine, or
investigate the article as appropriate.
(2) The Secretary shall request the Secretary of Treasury to remove an article held pursuant to
paragraph (1) to a secure facility, as appropriate. During the period of time that such article is
so held, the article shall not be transferred by any person from the port of entry into the United
States for the article, or from the secure facility to which the article has been removed, as the
case may be. Subsection (b) does not authorize the delivery of the article pursuant to the
execution of a bond while the article is so held.
(3) An officer or qualified employee of the Food and Drug Administration may make a request
under paragraph (1) only if the Secretary or an official designated by the Secretary approves
the request. An official may not be so designated unless the official is the director of the district
under this Act in which the article involved is located, or is an official senior to such director.
(4) With respect to an article of food for which a request under paragraph (1) is made, the
Secretary, promptly after the request is made, shall notify the State in which the port of entry
involved is located that the request has been made, and as applicable, that such article is
being held under this subsection.
(k) Importation by debarred persons.
(1) If an article of food is being imported or offered for import into the United States, and the
importer, owner, or consignee of the article is a person who has been debarred under section
306(b)(3), such article shall be held at the port of entry for the article, and may not be delivered
to such person. Subsection (b) does not authorize the delivery of the article pursuant to the
execution of a bond while the article is so held. The article shall be removed to a secure facility,
as appropriate. During the period of time that such article is so held, the article shall not be
transferred by any person from the port of entry into the United States for the article, or from
the secure facility to which the article has been removed, as the case may be.
(2) An article of food held under paragraph (1) may be delivered to a person who is not a
debarred person under section 306(b)(3) if such person affirmatively establishes, at the
expense of the person, that the article complies with the requirements of this Act, as
determined by the Secretary.
(l) Failure to register.
(1) 3 If an article of food is being imported or offered for import into the United States, and such
article is from a foreign facility for which a registration has not been submitted to the Secretary
under section 415, such article shall be held at the port of entry for the article, and may not be
delivered to the importer, owner, or consignee of the article, until the foreign facility is so
registered. Subsection (b) does not authorize the delivery of the article pursuant to the
execution of a bond while the article is so held. The article shall be removed to a secure facility,
as appropriate. During the period of time that such article is so held, the article shall not be
transferred by any person from the port of entry into the United States for the article, or from
the secure facility to which the article has been removed, as the case may be.
(m) Prior notice of imported food shipments.
(1) In the case of an article of food that is being imported or offered for import into the United
States, the Secretary, after consultation with the Secretary of the Treasury, shall by regulation
require, for the purpose of enabling such article to be inspected at ports of entry into the United
States, the submission to the Secretary of a notice providing the identity of each of the
following: The article; the manufacturer and shipper of the article; if known within the specified
period of time that notice is required to be provided, the grower of the article; the country from
which the article originates; the country from which the article is shipped; and the anticipated
port of entry for the article. An article of food imported or offered for import without submission
of such notice in accordance with the requirements under this paragraph shall be refused
admission into the United States . Nothing in this section may be construed as a limitation on
the port of entry for an article of food.
(2)(A) Regulations under paragraph (1) shall require that a notice under such paragraph be
provided by a specified period of time in advance of the time of the importation of the article of
food involved or the offering of the food for import, which period shall be no less than the
minimum amount of time necessary for the Secretary to receive, review, and appropriately
respond to such notification, but may not exceed five days. In determining the specified period
of time required under this subparagraph, the Secretary may consider, but is not limited to
consideration of, the effect on commerce of such period of time, the locations of the various
ports of entry into the United States, the various modes of transportation, the types of food
imported into the United States, and any other such consideration. Nothing in the preceding
sentence may be construed as a limitation on the obligation of the Secretary to receive, review,
and appropriately respond to any notice under paragraph (1).
(B)(i) If an article of food is being imported or offered for import into the United States and a
notice under paragraph (1) is not provided in advance in accordance with the requirements
under paragraph (1), such article shall be held at the port of entry for the article, and may not
be delivered to the importer, owner, or consignee of the article, until such notice is submitted to
the Secretary, and the Secretary examines the notice and determines that the notice is in
accordance with the requirements under paragraph (1). Subsection (b) does not authorize the
delivery of the article pursuant to the execution of a bond while the article is so held. The article
shall be removed to a secure facility, as appropriate. During the period of time that such article
is so held, the article shall not be transferred by any person from the port of entry into the
United States for the article, or from the secure facility to which the article has been removed,
as the case may be.
(ii) In carrying out clause (i) with respect to an article of food, the Secretary shall determine
whether there is in the possession of the Secretary any credible evidence or information
indicating that such article presents a threat of serious adverse health consequences or death
to humans or animals.
(3)(A) This subsection may not be construed as limiting the authority of the Secretary to obtain
information under any other provision of this Act.
(B) This subsection may not be construed as authorizing the Secretary to impose any
requirements with respect to a food to the extent that it is within the exclusive jurisdiction of the
Secretary of Agriculture pursuant to the Federal Meat Inspection Act (21 U.S.C. 601 et seq.),
the Poultry Products Inspection Act (21 U.S.C. 451 et seq.), or the Egg Products Inspection
Act (21 U.S.C. 1031 et seq.).
(n) Labeling of food refused admission.
(1) If a food has been refused admission under subsection (a), other than such a food that is
required to be destroyed, the Secretary may require the owner or consignee of the food to affix
to the container of the food a label that clearly and conspicuously bears the statement:
"UNITED STATES: REFUSED ENTRY".
(2) All expenses in connection with affixing a label under paragraph (1) shall be paid by the
owner or consignee of the food involved, and in default of such payment, shall constitute a lien
against future importations made by such owner or consignee.
(3) A requirement under paragraph (1) remains in effect until the Secretary determines that the
food involved has been brought into compliance with this Act.
(o) Registration statement. If an article that is a drug or device is being imported or offered for
import into the United States, and the importer, owner, or consignee of such article does not, at
the time of offering the article for import, submit to the Secretary a statement that identifies the
registration under section 510(i) of each establishment that with respect to such article is
required under such section to register with the Secretary, the article may be refused
admission. If the article is refused admission for failure to submit such a statement, the article
shall be held at the port of entry for the article, and may not be delivered to the importer, owner,
or consignee of the article, until such a statement is submitted to the Secretary. Subsection (b)
does not authorize the delivery of the article pursuant to the execution of a bond while the
article is so held. The article shall be removed to a secure facility, as appropriate. During the
period of time that such article is so held, the article shall not be transferred by any person
from the port of entry into the United States for the article, or from the secure facility to which
the article has been removed, as the case may be.
Prospective amendment:
Amendment of subsecs. (a) and (b), effective 1 year after enactment. Act Dec. 22, 2006, P.L.
109-462, § 5(a), 120 Stat. 3475 (effective 1 year after enactment, as provided by § 5(b) of such
Act, which appears as a note to this section), provides:
"Section 801 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 381) is amended--
"(1) in subsection (a), by inserting after the third sentence the following: 'If such article is
subject to a requirement under section 760 or 761 [21 USC §§ 379aa or 379aa-1] and if the
Secretary has credible evidence or information indicating that the responsible person (as
defined in such section 760 or 761) has not complied with a requirement of such section 760 or
761 with respect to any such article, or has not allowed access to records described in such
section 760 or 761, then such article shall be refused admission, except as provided in
subsection (b) of this section.'; and
"(2) in the second sentence of subsection (b)--
"(A) by inserting '(1)' before 'an article included';
"(B) by inserting before 'final determination' the following: 'or (2) with respect to an article
included within the provision of the fourth sentence of subsection (a), the responsible person
(as defined in section 760 or 761 [21 USC §§ 379aa or 379aa-1]) can take action that would
assure that the responsible person is in compliance with section 760 or 761 [21 USC §§ 379aa
or 379aa-1], as the case may be,'; and
"(C) by inserting ', or, with respect to clause (2), the responsible person,' before 'to perform'.".
EXPORTS OF CERTAIN UNAPPROVED PRODUCTS
SEC. 802. [21 U.S.C. 382] (a) A drug or device—
(1) which, in the case of a drug—
(A)(i) requires approval by the Secretary under section 505 before such drug may be
introduced or delivered for introduction into interstate commerce; or
(ii) requires licensing by the Secretary under section 351 of the Public Health Service Act or by
the Secretary of Agriculture under the Act of March 4, 1913 (known as the Virus-Serum Toxin
Act) before it may be introduced or delivered for introduction into interstate commerce;
(B) does not have such approval or license; and
(C) is not exempt from such sections or Act; and
(2) which, in the case of a device—
(A) does not comply with an applicable requirement under section 514 or 515;
(B) under section 520(g) is exempt from either such section; or
(C) is a banned device under section 516, is adulterated, misbranded, and in violation of such
sections or Act unless the export of the drug or device is, except as provided in subsection (f),
authorized under subsection (b), (c), (d), or (e) or section 801(e)(2). If 4 a drug or device
described in paragraphs (1) and (2) may be exported under subsection (b) and if an
application for such drug or device under section 505 or 515 or section 351 of the Public
Health Service Act was disapproved, the Secretary shall notify the appropriate public health
official of the country to which such drug will be exported of such disapproval.
(b)(1)(A) A drug or device described in subsection (a) may be exported to any country, if the
drug or device complies with the laws of that country and has valid marketing authorization by
the appropriate authority—
(i) in Australia, Canada, Israel, Japan, New Zealand, Switzerland, or South Africa; or
(ii) in the European Union or a country in the European Economic Area (the countries in the
European Union and the European Free Trade Association) if the drug or device is marketed
in that country or the drug or device is authorized for general marketing in the European
Economic Area.
(B) The Secretary may designate an additional country to be included in the list of countries
described in clauses (i) and (ii) of subparagraph (A) if all of the following requirements are met
in such country:
(i) Statutory or regulatory requirements which require the review of drugs and devices for
safety and effectiveness by an entity of the government of such country and which authorize
the approval of only those drugs and devices which have been determined to be safe and
effective by experts employed by or acting on behalf of such entity and qualified by scientific
training and experience to evaluate the safety and effectiveness of drugs and devices on the
basis of adequate and well-controlled investigations, including clinical investigations,
conducted by experts qualified by scientific training and experience to evaluate the safety and
effectiveness of drugs and devices.
(ii) Statutory or regulatory requirements that the methods used in, and the facilities and
controls used for—
(I) the manufacture, processing, and packing of drugs in the country are adequate to preserve
their identity, quality, purity, and strength; and
(II) the manufacture, preproduction design validation, packing, storage, and installation of a
device are adequate to assure that the device will be safe and effective.
(iii) Statutory or regulatory requirements for the reporting of adverse reactions to drugs and
devices and procedures to withdraw approval and remove drugs and devices found not to be
safe or effective.
(iv) Statutory or regulatory requirements that the labeling and promotion of drugs and devices
must be in accordance with the approval of the drug or device.
(v) The valid marketing authorization system in such country or countries is equivalent to the
systems in the countries described in clauses (i) and (ii) of subparagraph (A).
The Secretary shall not delegate the authority granted under this subparagraph.
(C) An appropriate country official, manufacturer, or exporter may request the Secretary to
take action under subparagraph (B) to designate an additional country or countries to be
added to the list of countries described in clauses (i) and (ii) of subparagraph (A) by submitting
documentation to the Secretary in support of such designation. Any person other than a
country requesting such designation shall include, along with the request, a letter from the
country indicating the desire of such country to be designated.
(2) A drug described in subsection (a) may be directly exported to a country which is not listed
in clause (i) or (ii) of paragraph (1)(A) if—
(A) the drug complies with the laws of that country and has valid marketing authorization by the
responsible authority in that country; and
(B) the Secretary determines that all of the following requirements are met in that country:
(i) Statutory or regulatory requirements which require the review of drugs for safety and
effectiveness by an entity of the government of such country and which authorize the approval
of only those drugs which have been determined to be safe and effective by experts employed
by or acting on behalf of such entity and qualified by scientific training and experience to
evaluate the safety and effectiveness of drugs on the basis of adequate and well-controlled
investigations, including clinical investigations, conducted by experts qualified by scientific
training and experience to evaluate the safety and effectiveness of drugs.
(ii) Statutory or regulatory requirements that the methods used in, and the facilities and
controls used for the manufacture, processing, and packing of drugs in the country are
adequate to preserve their identity, quality, purity, and strength.
(iii) Statutory or regulatory requirements for the reporting of adverse reactions to drugs and
procedures to withdraw approval and remove drugs found not to be safe or effective.
(iv) Statutory or regulatory requirements that the labeling and promotion of drugs must be in
accordance with the approval of the drug.
(3) The exporter of a drug described in subsection (a) which would not meet the conditions for
approval under this Act or conditions for approval of a country described in clause (i) or (ii) of
paragraph (1)(A) may petition the Secretary for authorization to export such drug to a country
which is not described in clause (i) or (ii) of paragraph (1)(A) or which is not described in
paragraph (2). The Secretary shall permit such export if—
(A) the person exporting the drug—
(i) certifies that the drug would not meet the conditions for approval under this Act or the
conditions for approval of a country described in clause (i) or (ii) of paragraph (1)(A); and
(ii) provides the Secretary with credible scientific evidence, acceptable to the Secretary, that
the drug would be safe and effective under the conditions of use in the country to which it is
being exported; and
(B) the appropriate health authority in the country to which the drug is being exported—
(i) requests approval of the export of the drug to such country;
(ii) certifies that the health authority understands that the drug is not approved under this Act or
in a country described in clause (i) or (ii) of paragraph (1)(A); and
(iii) concurs that the scientific evidence provided pursuant to subparagraph (A) is credible
scientific evidence that the drug would be reasonably safe and effective in such country.
The Secretary shall take action on a request for export of a drug under this paragraph within
60 days of receiving such request.
(c) A drug or device intended for investigational use in any country described in clause (i) or (ii)
of subsection (b)(1)(A) may be exported in accordance with the laws of that country and shall
be exempt from regulation under section 505(i) or 520(g).
(d) A drug or device intended for formulation, filling, packaging, labeling, or further processing
in anticipation of market authorization in any country described in clause (i) or (ii) of subsection
(b)(1)(A) may be exported for use in accordance with the laws of that country.
(e)(1) A drug or device which is used in the diagnosis, prevention, or treatment of a tropical
disease or another disease not of significant prevalence in the United States and which does
not otherwise qualify for export under this section shall, upon approval of an application, be
permitted to be exported if the Secretary finds that the drug or device will not expose patients
in such country to an unreasonable risk of illness or injury and the probable benefit to health
from the use of the drug or device (under conditions of use prescribed, recommended, or
suggested in the labeling or proposed labeling of the drug or device) outweighs the risk of
injury or illness from its use, taking into account the probable risks and benefits of currently
available drug or device treatment.
(2) The holder of an approved application for the export of a drug or device under this
subsection shall report to the Secretary—
(A) the receipt of any credible information indicating that the drug or device is being or may
have been exported from a country for which the Secretary made a finding under paragraph
(1)(A) to a country for which the Secretary cannot make such a finding; and
(B) the receipt of any information indicating adverse reactions to such drug.
(3)(A) If the Secretary determines that—
(i) a drug or device for which an application is approved under paragraph (1) does not continue
to meet the requirements of such paragraph; or
(ii) the holder of an approved application under paragraph (1) has not made the report required
by paragraph (2), the Secretary may, after providing the holder of the application an
opportunity for an informal hearing, withdraw the approved application.
(B) If the Secretary determines that the holder of an approved application under paragraph (1)
or an importer is exporting a drug or device from the United States to an importer and such
importer is exporting the drug or device to a country for which the Secretary cannot make a
finding under paragraph (1) and such export presents an imminent hazard, the Secretary shall
immediately prohibit the export of the drug or device to such importer, provide the person
exporting the drug or device from the United States prompt notice of the prohibition, and afford
such person an opportunity for an expedited hearing.
(f) A drug or device may not be exported under this section—
(1) if the drug or device is not manufactured, processed, packaged, and held in substantial
conformity with current good manufacturing practice requirements or does not meet
international standards as certified by an international standards organization recognized by
the Secretary;
(2) if the drug or device is adulterated under clause (1), (2)(A), or (3) of section 501(a) or
subsection (c) or (d) of section 501;
(3) if the requirements of subparagraphs (A) through (D) of section 801(e)(1) have not been
met;
(4)(A) if the drug or device is the subject of a notice by the Secretary or the Secretary of
Agriculture of a determination that the probability of reimportation of the exported drug or
device would present an imminent hazard to the public health and safety of the United States
and the only means of limiting the hazard is to prohibit the export of the drug or device; or
(B) if the drug or device presents an imminent hazard to the public health of the country to
which the drug or device would be exported;
(5) if the labeling of the drug or device is not—
(A) in accordance with the requirements and conditions for use in—
(i) the country in which the drug or device received valid marketing authorization under
subsection (b); and
(ii) the country to which the drug or device would be exported; and
(B) in the language and units of measurement of the country to which the drug or device would
be exported or in the language designated by such country; or
(6) if the drug or device is not promoted in accordance with the labeling requirements set forth
in paragraph (5).
In making a finding under paragraph (4)(B), (5), or (6) the Secretary shall consult with the
appropriate public health official in the affected country.
(g) The exporter of a drug or device exported under subsection (b)(1) shall provide a simple
notification to the Secretary identifying the drug or device when the exporter first begins to
export such drug or device to any country listed in clause (i) or (ii) of subsection (b)(1)(A).
When an exporter of a drug or device first begins to export a drug or device to a country which
is not listed in clause (i) or (ii) of subsection (b)(1)A) 5 , the exporter shall provide a simple
notification to the Secretary identifying the drug or device and the country to which such drug
or device is being exported. Any exporter of a drug or device shall maintain records of all drugs
or devices exported and the countries to which they were exported.
(h) For purposes of this section—
(1) a reference to the Secretary shall in the case of a biological product which is required to be
licensed under the Act of March 4, 1913 (37 Stat. 832–833) (commonly known as the
Virus-Serum Toxin Act) be considered to be a reference to the Secretary of Agriculture, and
(2) the term "drug" includes drugs for human use as well as biologicals under section 351 of
the Public Health Service Act or the Act of March 4, 1913 (37 Stat. 832–833) (commonly
known as the Virus-Serum Toxin Act).
(i) Insulin and antibiotic drugs may be exported without regard to the requirements in this
section if the insulin and antibiotic drugs meet the requirements of section 801(e)(1).
OFFICE OF INTERNATIONAL RELATIONS
SEC. 803. [21 U.S.C. 383] (a) There is established in the Department of Health and Human
Services an Office of International Relations.
(b) In carrying out the functions of the office under subsection (a), the Secretary may enter into
agreements with foreign countries to facilitate commerce in devices between the United States
and such countries consistent with the requirements of this Act. In such agreements, the
Secretary shall encourage the mutual recognition of—
(1) good manufacturing practice regulations promulgated under section 520(f), and
(2) other regulations and testing protocols as the Secretary determines to be appropriate.
(c)(1) The Secretary shall support the Office of the United States Trade Representative, in
consultation with the Secretary of Commerce, in meetings with representatives of other
countries to discuss methods and approaches to reduce the burden of regulation and
harmonize regulatory requirements if the Secretary determines that such harmonization
continues consumer protections consistent with the purposes of this Act.
(2) The Secretary shall support the Office of the United States Trade Representative, in
consultation with the Secretary of Commerce, in efforts to move toward the acceptance of
mutual recognition agreements relating to the regulation of drugs, biological products, devices,
foods, food additives, and color additives, and the regulation of good manufacturing practices,
between the European Union and the United States.
(3) The Secretary shall regularly participate in meetings with representatives of other foreign
governments to discuss and reach agreement on methods and approaches to harmonize
regulatory requirements.
(4) The Secretary shall, not later than 180 days after the date of enactment of the Food and
Drug Administration Modernization Act of 1997, make public a plan that establishes a
framework for achieving mutual recognition of good manufacturing practices inspections.
(5) Paragraphs (1) through (4) shall not apply with respect to products defined in section
201(ff).
SEC. 804. [21 U.S.C. 384] IMPORTATION OF PRESCRIPTION DRUGS.
(a) DEFINITIONS--In this section:
(1) IMPORTER--The term "importer" means a pharmacist or wholesaler.
(2) PHARMACIST.--The term "pharmacist" means a person licensed by a State to practice
pharmacy, including the dispensing and selling of prescription drugs.
(3) PRESCRIPTION DRUG.--The term "prescription drug" means a drug subject to section
503(b), other than--
(A) a controlled substance (as defined in section 102 of the Controlled Substances Act (21
U.S.C. 802));
(B) a biological product (as defined in section 351 of the Public Health Service Act (42 U.S.C.
262));
(C) an infused drug (including a peritoneal dialysis solution);
(D) an intravenously injected drug;
(E) a drug that is inhaled during surgery; or
(F) a drug which is a parenteral drug, the importation of which pursuant to subsection (b) is
determined by the Secretary to pose a threat to the public health, in which case section
801(d)(1) shall continue to apply.
(4) QUALIFYING LABORATORY.--The term "qualifying laboratory" means a laboratory in the
United States that has been approved by the Secretary for the purposes of this section.
(5) WHOLESALER.--
(A) IN GENERAL.--The term "wholesaler" means a person licensed as a wholesaler or
distributor of prescription drugs in the United States under section 503(e)(2)(A).
(B) EXCLUSION.--The term "wholesaler" does not include a person authorized to import drugs
under section 801(d)(1).
(b) REGULATIONS.--The Secretary, after consultation with the United States Trade
Representative and the Commissioner of Customs, shall promulgate regulations permitting
pharmacists and wholesalers to import prescription drugs from Canada into the United States .
(c) LIMITATION.--The regulations under subsection (b) shall--
(1) require that safeguards be in place to ensure that each prescription drug imported under
the regulations complies with section 505 (including with respect to being safe and effective for
the intended use of the prescription drug), with sections 501 and 502, and with other
applicable requirements of this Act;
(2) require that an importer of a prescription drug under the regulations comply with
subsections (d)(1) and (e); and
(3) contain any additional provisions determined by the Secretary to be appropriate as a
safeguard to protect the public health or as a means to facilitate the importation of prescription
drugs.
(d) INFORMATION AND RECORDS.--
(1) IN GENERAL.--The regulations under subsection (b) shall require an importer of a
prescription drug under subsection (b) to submit to the Secretary the following information and
documentation:
(A) The name and quantity of the active ingredient of the prescription drug.
(B) A description of the dosage form of the prescription drug.
(C) The date on which the prescription drug is shipped.
(D) The quantity of the prescription drug that is shipped.
(E) The point of origin and destination of the prescription drug.
(F) The price paid by the importer for the prescription drug.
(G) Documentation from the foreign seller specifying--
(i) the original source of the prescription drug; and
(ii) the quantity of each lot of the prescription drug originally received by the seller from that
source.
(H) The lot or control number assigned to the prescription drug by the manufacturer of the
prescription drug.
(I) The name, address, telephone number, and professional license number (if any) of the
importer.
(J)(i) In the case of a prescription drug that is shipped directly from the first foreign recipient of
the prescription drug from the manufacturer:
(I) Documentation demonstrating that the prescription drug was received by the recipient from
the manufacturer and subsequently shipped by the first foreign recipient to the importer.
(II) Documentation of the quantity of each lot of the prescription drug received by the first
foreign recipient demonstrating that the quantity being imported into the United States is not
more than the quantity that was received by the first foreign recipient.
(III)(aa) In the case of an initial imported shipment, documentation demonstrating that each
batch of the prescription drug in the shipment was statistically sampled and tested for
authenticity and degradation.
(bb) In the case of any subsequent shipment, documentation demonstrating that a statistically
valid sample of the shipment was tested for authenticity and degradation.
(ii) In the case of a prescription drug that is not shipped directly from the first foreign recipient
of the prescription drug from the manufacturer, documentation demonstrating that each batch
in each shipment offered for importation into the United States was statistically sampled and
tested for authenticity and degradation.
(K) Certification from the importer or manufacturer of the prescription drug that the prescription
drug--
(i) is approved for marketing in the United States and is not adulterated or misbranded; and
(ii) meets all labeling requirements under this Act.
(L) Laboratory records, including complete data derived from all tests necessary to ensure that
the prescription drug is in compliance with established specifications and standards.
(M) Documentation demonstrating that the testing required by subparagraphs (J) and (L) was
conducted at a qualifying laboratory.
(N) Any other information that the Secretary determines is necessary to ensure the protection
of the public health.
(2) MAINTENANCE BY THE SECRETARY.--The Secretary shall maintain information and
documentation submitted under paragraph (1) for such period of time as the Secretary
determines to be necessary.
(e) TESTING.--The regulations under subsection (b) shall require--
(1) that testing described in subparagraphs (J) and (L) of subsection (d)(1) be conducted by
the importer or by the manufacturer of the prescription drug at a qualified laboratory;
(2) if the tests are conducted by the importer--
(A) that information needed to--
(i) authenticate the prescription drug being tested; and
(ii) confirm that the labeling of the prescription drug complies with labeling requirements under
this Act;
be supplied by the manufacturer of the prescription drug to the pharmacist or wholesaler; and
(B) that the information supplied under subparagraph (A) be kept in strict confidence and used
only for purposes of testing or otherwise complying with this Act; and
(3) may include such additional provisions as the Secretary determines to be appropriate to
provide for the protection of trade secrets and commercial or financial information that is
privileged or confidential.
(f) REGISTRATION OF FOREIGN SELLERS.--Any establishment within Canada engaged in
the distribution of a prescription drug that is imported or offered for importation into the United
States shall register with the Secretary the name and place of business of the establishment
and the name of the United States agent for the establishment.
(g) SUSPENSION OF IMPORTATION.--The Secretary shall require that importations of a
specific prescription drug or importations by a specific importer under subsection (b) be
immediately suspended on discovery of a pattern of importation of that specific prescription
drug or by that specific importer of drugs that are counterfeit or in violation of any requirement
under this section, until an investigation is completed and the Secretary determines that the
public is adequately protected from counterfeit and violative prescription drugs being imported
under subsection (b).
(h) APPROVED LABELING.--The manufacturer of a prescription drug shall provide an
importer written authorization for the importer to use, at no cost, the approved labeling for the
prescription drug.
(i) CHARITABLE CONTRIBUTIONS.--Notwithstanding any other provision of this section,
section 801(d)(1) continues to apply to a prescription drug that is donated or otherwise
supplied at no charge by the manufacturer of the drug to a charitable or humanitarian
organization (including the United Nations and affiliates) or to a government of a foreign
country.
(j) WAIVER AUTHORITY FOR IMPORTATION BY INDIVIDUALS.--
(1) DECLARATIONS.--Congress declares that in the enforcement against individuals of the
prohibition of importation of prescription drugs and devices, the Secretary should--
(A) focus enforcement on cases in which the importation by an individual poses a significant
threat to public health; and
(B) exercise discretion to permit individuals to make such importations in circumstances in
which--
(i) the importation is clearly for personal use; and
(ii) the prescription drug or device imported does not appear to present an unreasonable risk to
the individual.
(2) WAIVER AUTHORITY.--
(A) IN GENERAL.--The Secretary may grant to individuals, by regulation or on a case-by-case
basis, a waiver of the prohibition of importation of a prescription drug or device or class of
prescription drugs or devices, under such conditions as the Secretary determines to be
appropriate.
(B) GUIDANCE ON CASE-BY-CASE WAIVERS.--The Secretary shall publish, and update as
necessary, guidance that accurately describes circumstances in which the Secretary will
consistently grant waivers on a case-by-case basis under subparagraph (A), so that
individuals may know with the greatest practicable degree of certainty whether a particular
importation for personal use will be permitted.
(3) DRUGS IMPORTED FROM CANADA.--In particular, the Secretary shall by regulation
grant individuals a waiver to permit individuals to import into the United States a prescription
drug that--
(A) is imported from a licensed pharmacy for personal use by an individual, not for resale, in
quantities that do not exceed a 90-day supply;
(B) is accompanied by a copy of a valid prescription;
(C) is imported from Canada, from a seller registered with the Secretary;
(D) is a prescription drug approved by the Secretary under chapter V;
(E) is in the form of a final finished dosage that was manufactured in an establishment
registered under section 510; and
(F) is imported under such other conditions as the Secretary determines to be necessary to
ensure public safety.
(k) CONSTRUCTION--Nothing in this section limits the authority of the Secretary relating to
the importation of prescription drugs, other than with respect to section 801(d)(1) as provided
in this section.
(l) EFFECTIVENESS OF SECTION.--
(1) COMMENCEMENT OF PROGRAM.--This section shall become effective only if the
Secretary certifies to the Congress that the implementation of this section will--
(A) pose no additional risk to the public's health and safety; and
(B) result in a significant reduction in the cost of covered products to the American consumer.
(2) TERMINATION OF PROGRAM.--
(A) IN GENERAL.--If, after the date that is 1 year after the effective date of the regulations
under subsection (b) and before the date that is 18 months after the effective date, the
Secretary submits to Congress a certification that, in the opinion of the Secretary, based on
substantial evidence obtained after the effective date, the benefits of implementation of this
section do not outweigh any detriment of implementation of this section, this section shall
cease to be effective as of the date that is 30 days after the date on which the Secretary
submits the certification.
(B) PROCEDURE.--The Secretary shall not submit a certification under subparagraph (A)
unless, after a hearing on the record under sections 556 and 557 of title 5, United States Code,
the Secretary--
(i)(I) determines that it is more likely than not that implementation of this section would result in
an increase in the risk to the public health and safety;
(II) identifies specifically, in qualitative and quantitative terms, the nature of the increased risk;
(III) identifies specifically the causes of the increased risk; and
(IV)(aa) considers whether any measures can be taken to avoid, reduce, or mitigate the
increased risk; and
(bb) if the Secretary determines that any measures described in item (aa) would require
additional statutory authority, submits to Congress a report describing the legislation that
would be required;
(ii) identifies specifically, in qualitative and quantitative terms, the benefits that would result
from implementation of this section (including the benefit of reductions in the cost of covered
products to consumers in the United States, allowing consumers to procure needed
medication that consumers might not otherwise be able to procure without foregoing other
necessities of life); and
(iii)(I) compares in specific terms the detriment identified under clause (i) with the benefits
identified under clause (ii); and
(II) determines that the benefits do not outweigh the detriment.
(m) AUTHORIZATION OF APPROPRIATIONS.--There are authorized to be appropriated
such sums as are necessary to carry out this section.
Footnotes: Chapter VIII
1. So in law. Probably should be "subsection".
2. Subsections (h) and (i) were added by section 302 of Public Law 107–188 (116 Stat. 662).
In such section 302, subsection (f) provides as follows:
(f) AUTHORIZATION OF APPROPRIATIONS.—For the purpose of carrying out this section
and the amendments made by this section, there are authorized to be appropriated
$100,000,000 for fiscal year 2002, and such sums as may be necessary for each of the fiscal
years 2003 through 2006, in addition to other authorizations of appropriations that are
available for such purpose.
3. So in law. There is no paragraph (2). See section 305(c) of Public Law 107–188 (116 Stat.
668).
4. Placement of sentence is so in law. See section 2102(d)(1) of Public Law 104–134 (chapter
1A of title II; 110 Stat. 1321-313, 1321-315). Sentence probably should appear after and below
subparagraph (C), with the same indentation as the section designation.
5. So in law. See section 2102(d)(1) of Public Law 104–134 (chapter 1A of title II; 110 Stat.
1321-315, 1321-319). Probably should have a beginning parentheses before "A)".
CHAPTER IX--MISCELLANEOUS
SEPARABILITY CLAUSE
SEC. 901. [21 U.S.C. 391] If any provision of this Act is declared unconstitutional, or the
applicability thereof to any person or circumstances is held invalid, the constitutionality of the
remainder of the Act and the applicability thereof to other persons and circumstances shall not
be affected thereby.
EFFECTIVE DATE AND REPEALS
SEC. 902. [21 U.S.C. 392] (a) This Act shall take effect twelve months after the date of its
enactment. The Federal Food and Drug Act of June 30, 1906, as amended (U.S.C., 1934 ed.,
title 21, secs.1–15), shall remain in force until such effective date, and except as otherwise
provided in this subsection, is hereby repealed effective upon such date: Provided, That the
provisions of section 701 shall become effective on the enactment of this Act, and thereafter
the Secretary [of Agriculture] is authorized hereby to (1) conduct hearings and to promulgate
regulations which shall become effective on or after the effective date of this Act as the
Secretary [of Agriculture] shall direct, and (2) designate prior to the effective date of this Act
food having common or usual names and exempt such food from the requirements of clause
(2) of section 403(i) for a reasonable time to permit the formulation, promulgation, and effective
application of definitions and standards of identity therefor as provided by section 401:
Provided further, That sections 502(j), 505, and 601(a), and all other provisions of this Act to
the extent that they may relate to the enforcement of such sections, shall take effect on the
date of the enactment of this Act, except that in the case of a cosmetic to which the proviso of
section 601(a) relates, such cosmetic shall not, prior to the ninetieth day after such date of
enactment, be deemed adulterated by reason of the failure of its label to bear the legend
prescribed in such proviso: Provided further, That the Act of March 4, 1923 (U.S.C., 1945 ed.,
title 21, sec. 321a; 32 Stat. 1500, ch. 268), defining butter and providing a standard therefor;
the Act of July 24, 1919 (U.S.C., 1946 ed., title 21, sec. 321b; 41 Stat. 271, ch. 26), defining
wrapped meats as in package form; and the amendment to the Food and Drug Act, section
10A, approved August 27, 1935 (U.S.C., 1946 ed., title 21, sec. 372a [49 Stat. 871, ch. 739]),
shall remain in force and effect and be applicable to the provisions of this Act.
(b) Meats and meat food products shall be exempt from the provisions of this Act to the extent
of the application or the extension thereto of the Meat Inspection Act, approved March 4, 1907,
as amended (U.S.C., 1946 ed., title 21, secs. 71–96; 34 Stat. 1260 et seq.).
(c) Nothing contained in this Act shall be construed as in any way affecting, modifying,
repealing, or superseding the provisions of section 351 of Public Health Service Act (relating to
viruses, serums, toxins, and analogous products applicable to man); the virus, serum, toxin,
and analogous products provisions, applicable to domestic animals, of the Act of Congress
approved March 4, 1913 (37 Stat. 832–833); the Filled Cheese Act of June 6, 1896 (U.S.C.,
1946 ed., title 26, ch. 17, secs. 2350–2362); the Filled Milk Act of March 4, 1923 (U.S.C. 1946
ed., title 21, ch. 3, secs. 61–64); or the Import Milk Act of February 15, 1927 (U.S.C., 1946 ed.,
title 21, ch. 4, secs. 141–149).
SEC. 903. [ 21 U.S.C. 393] FOOD AND DRUG ADMINISTRATION.
(a) IN GENERAL.—There is established in the Department of Health and Human Services the
Food and Drug Administration (hereinafter in this section referred to as the ‘‘Administration’’).
(b) MISSION.—The Administration shall—
(1) promote the public health by promptly and efficiently reviewing clinical research and taking
appropriate action on the marketing of regulated products in a timely manner;
(2) with respect to such products, protect the public health by ensuring that—
(A) foods are safe, wholesome, sanitary, and properly labeled;
(B) human and veterinary drugs are safe and effective;
(C) there is reasonable assurance of the safety and effectiveness of devices intended for
human use;
(D) cosmetics are safe and properly labeled; and
(E) public health and safety are protected from electronic product radiation;
(3) participate through appropriate processes with representatives of other countries to reduce
the burden of regulation, harmonize regulatory requirements, and achieve appropriate
reciprocal arrangements; and
(4) as determined to be appropriate by the Secretary, carry out paragraphs (1) through (3) in
consultation with experts in science, medicine, and public health, and in cooperation with
consumers, users, manufacturers, importers, packers, distributors, and retailers of regulated
products.
(c) INTERAGENCY COLLABORATION.—The Secretary shall implement programs and
policies that will foster collaboration between the Administration, the National Institutes of
Health, and other science-based Federal agencies, to enhance the scientific and technical
expertise available to the Secretary in the conduct of the duties of the Secretary with respect to
the development, clinical investigation, evaluation, and postmarket monitoring of emerging
medical therapies, including complementary therapies, and advances in nutrition and food
science.
(d) COMMISSIONER.—
(1) APPOINTMENT.—There shall be in the Administration a Commissioner of Food and Drugs
(hereinafter in this section referred to as the ‘‘Commissioner’’) who shall be appointed by the
President by and with the advice and consent of the Senate.
(2) GENERAL POWERS.—The Secretary, through the Commissioner, shall be responsible for
executing this Act and for—
(A) providing overall direction to the Food and Drug Administration and establishing and
implementing general policies respecting the management and operation of programs and
activities of the Food and Drug Administration;
(B) coordinating and overseeing the operation of all administrative entities within the
Administration;
(C) research relating to foods, drugs, cosmetics, and devices in carrying out this Act;
(D) conducting educational and public information programs relating to the responsibilities of
the Food and Drug Administration; and
(E) performing such other functions as the Secretary may prescribe.
(e) TECHNICAL AND SCIENTIFIC REVIEW GROUPS.—The Secretary through the
Commissioner of Food and Drugs may, without regard to the provisions of title 5, United States
Code, governing appointments in the competitive service and without regard to the provisions
of chapter 51 and subchapter III of chapter 53 of such title relating to classification and General
Schedule pay rates, establish such technical and scientific review groups as are needed to
carry out the functions of the Administration, including functions under the Federal Food, Drug,
and Cosmetic Act, and appoint and pay the members of such groups, except that officers and
employees of the United States shall not receive additional compensation for service as
members of such groups.
(f) AGENCY PLAN FOR STATUTORY COMPLIANCE.—
(1) IN GENERAL.—Not later than 1 year after the date of enactment of the Food and Drug
Administration Modernization Act of 1997, the Secretary, after consultation with appropriate
scientific and academic experts, health care professionals, representatives of patient and
consumer advocacy groups, and the regulated industry, shall develop and publish in the
Federal Register a plan bringing the Secretary into compliance with each of the obligations of
the Secretary under this Act. The Secretary shall review the plan biannually and shall revise
the plan as necessary, in consultation with such persons.
(2) OBJECTIVES OF AGENCY PLAN.—The plan required by paragraph (1) shall establish
objectives and mechanisms to achieve such objectives, including objectives related to—
(A) maximizing the availability and clarity of information about the process for review of
applications and submissions (including petitions, notifications, and any other similar forms of
request) made under this Act;
(B) maximizing the availability and clarity of information for consumers and patients concerning
new products;
(C) implementing inspection and postmarket monitoring provisions of this Act;
(D) ensuring access to the scientific and technical expertise needed by the Secretary to meet
obligations described in paragraph (1);
(E) establishing mechanisms, by July 1, 1999, for meeting the time periods specified in this Act
for the review of all applications and submissions described in subparagraph (A) and
submitted after the date of enactment of the Food and Drug Administration Modernization Act
of 1997; and
(F) eliminating backlogs in the review of applications and submissions described in
subparagraph (A), by January 1, 2000.
(g) ANNUAL REPORT.—The Secretary shall annually prepare and publish in the Federal
Register and solicit public comment on a report that—
(1) provides detailed statistical information on the performance of the Secretary under the plan
described in subsection (f);
(2) compares such performance of the Secretary with the objectives of the plan and with the
statutory obligations of the Secretary; and
(3) identifies any regulatory policy that has a significant negative impact on compliance with
any objective of the plan or any statutory obligation and sets forth any proposed revision to any
such regulatory policy.
Sec. 904. [21 U.S.C.394] SCIENTIFIC REVIEW GROUPS.
Without regard to the provisions of title 5, United States Code, governing appointments in the
competitive service and without regard to the provisions of chapter 51 and subchapter III of
chapter 53 of such title relating to classification and General Schedule pay rates, the
Commissioner of Food and Drugs may—
(1) establish such technical and scientific review groups as are needed to carry out the
functions of the Food and Drug Administration (including functions prescribed under this Act);
and
(2) appoint and pay the members of such groups, except that officers and employees of the
United States shall not receive additional compensation for service as members of such
groups.
SEC. 905. [ 21 U.S.C. 395] LOAN REPAYMENT PROGRAM.
(a) IN GENERAL.—
(1) AUTHORITY FOR PROGRAM.—Subject to paragraph (2), the Secretary shall carry out a
program of entering into contracts with appropriately qualified health professionals under
which such health professionals agree to conduct research, as employees of the Food and
Drug Administration, in consideration of the Federal Government agreeing to repay, for each
year of such service, not more than $20,000 of the principal and interest of the educational
loans of such health professionals.
(2) LIMITATION.—The Secretary may not enter into an agreement with a health professional
pursuant to paragraph (1) unless such professional—
(A) has a substantial amount of educational loans relative to income; and
(B) agrees to serve as an employee of the Food and Drug Administration for purposes of
paragraph (1) for a period of not less than 3 years.
(b) APPLICABILITY OF CERTAIN PROVISIONS.—With respect to the National Health
Service Corps Loan Repayment Program established in subpart III of part D of title III of the
Public Health Service Act, the provisions of such subpart shall, except as inconsistent with
subsection (a) of this section, apply to the program established in such subsection in the same
manner and to the same extent as such provisions apply to the National Health Service Corps
Loan Repayment Program.
(c) AUTHORIZATION OF APPROPRIATIONS.—For the purpose of carrying out this section,
there are authorized to be appropriated such sums as may be necessary for each of the fiscal
years 1994 through 1996.
SEC. 906. [ 21 U.S.C. 396] PRACTICE OF MEDICINE.
Nothing in this Act shall be construed to limit or interfere with the authority of a health care
practitioner to prescribe or administer any legally marketed device to a patient for any
condition or disease within a legitimate health care practitioner-patient relationship. This
section shall not limit any existing authority of the Secretary to establish and enforce
restrictions on the sale or distribution, or in the labeling, of a device that are part of a
determination of substantial equivalence, established as a condition of approval, or
promulgated through regulations. Further, this section shall not change any existing prohibition
on the promotion of unapproved uses of legally marketed devices.
SEC. 907. [ 21 U.S.C. 397] CONTRACTS FOR EXPERT REVIEW.
(a) IN GENERAL.—
(1) AUTHORITY.—The Secretary may enter into a contract with any organization or any
individual (who is not an employee of the Department) with relevant expertise, to review and
evaluate, for the purpose of making recommendations to the Secretary on, part or all of any
application or submission (including a petition, notification, and any other similar form of
request) made under this Act for the approval or classification of an article or made under
section 351(a) of the Public Health Service Act (42 U.S.C. 262(a)) with respect to a biological
product. Any such contract shall be subject to the requirements of section 708 relating to the
confidentiality of information.
(2) INCREASED EFFICIENCY AND EXPERTISE THROUGH CONTRACTS.—The Secretary
may use the authority granted in paragraph (1) whenever the Secretary determines that use of
a contract described in paragraph (1) will improve the timeliness of the review of an application
or submission described in paragraph (1), unless using such authority would reduce the quality,
or unduly increase the cost, of such review. The Secretary may use such authority whenever
the Secretary determines that use of such a contract will improve the quality of the review of an
application or submission described in paragraph (1), unless using such authority would
unduly increase the cost of such review. Such improvement in timeliness or quality may
include providing the Secretary increased scientific or technical expertise that is necessary to
review or evaluate new therapies and technologies.
(b) REVIEW OF EXPERT REVIEW.—
(1) IN GENERAL.—Subject to paragraph (2), the official of the Food and Drug Administration
responsible for any matter for which expert review is used pursuant to subsection (a) shall
review the recommendations of the organization or individual who conducted the expert review
and shall make a final decision regarding the matter in a timely manner.
(2) LIMITATION.—A final decision by the Secretary on any such application or submission
shall be made within the applicable prescribed time period for review of the matter as set forth
in this Act or in the Public Health Service Act (42 U.S.C. 201 et seq.).
SEC. 908. [21 USC 398] NOTICES TO STATES REGARDING IMPORTED FOOD.
(a) IN GENERAL..--If the Secretary has credible evidence or information indicating that a
shipment of imported food or portion thereof presents a threat of serious adverse health
consequences or death to humans or animals, the Secretary shall provide notice regarding
such threat to the States in which the food is held or will be held, and to the States in which the
manufacturer, packer, or distributor of the food is located, to the extent that the Secretary has
knowledge of which States are so involved. In providing notice to a State, the Secretary shall
request the State to take such action as the State considers appropriate, if any, to protect the
public health regarding the food involved.
(b) RULE OF CONSTRUCTION.--Subsection (a) may not be construed as limiting the
authority of the Secretary with respect to food under any other provision of this Act.
SEC. 909. [21 USC 399] GRANTS TO STATES FOR INSPECTIONS.
(a) IN GENERAL.--The Secretary is authorized to make grants to States, territories, and Indian
tribes (as defined in section 4(e) of the Indian Self-Determination and Education Assistance
Act (25 U.S.C. 450b(e))) that undertake examinations, inspections, and investigations, and
related activities under section 702. The funds provided under such grants shall only be
available for the costs of conducting such examinations, inspections, investigations, and
related activities.
(b) NOTICES REGARDING ADULTERATED IMPORTED FOOD.--The Secretary may make
grants to the States for the purpose of assisting the States with the costs of taking appropriate
action to protect the public health in response to notification under section 908, including
planning and otherwise preparing to take such action.
(c) AUTHORIZATION OF APPROPRIATIONS.--For the purpose of carrying out this section,
there are authorized to be appropriated $10,000,000 for fiscal year 2002, and such sums as
may be necessary for each of the fiscal years 2003 through 2006.
APPENDIX
• Section 107(c) of Drug Amendments of 1962
• Public Law 88-136; Revolving Fund
• Section 108 of Animal Drug Amendments of 1968
• Section 5 of Orphan Drug Act
SECTION 107(c) OF DRUG AMENDMENTS OF 1962 1
(c)(1) As used in this subsection the term "enactment date" means the date of enactment of
this Act; and the term "basic Act" means the Federal Food, Drug, and Cosmetic Act.
(2) An application filed pursuant to section 505(b) of the basic Act which was "effective" within
the meaning of that Act on the day immediately preceding the enactment date shall be
deemed, as of the enactment date, to be an application "approved" by the Secretary within the
meaning of the basic Act as amended by this Act.
(3) In the case of any drug with respect to which an application filed under section 505(b) of the
basic Act is deemed to be an approved application on the enactment date by virtue of
paragraph (2) of this subsection—
(A) the amendments made by this Act to section 201(p), and to subsections (b) and (d) of
section 505, of the basic Act, insofar as such amendments relate to the effectiveness of drugs,
shall not, so long as approval of such application is not withdrawn or suspended pursuant to
section 505(e) of that Act, apply to such drug when intended solely for use under conditions
prescribed, recommended, or suggested in labeling covered by such approved application, but
shall apply to any changed use, or conditions of use, prescribed, recommended, or suggested
in its labeling, including such conditions of use as are the subject of an amendment or
supplement to such application pending on, or filed after, the enactment date; and
(B) clause (3) of the first sentence of section 505(e) of the basic Act, as amended by this Act,
shall not apply to such drug when intended solely for use under conditions prescribed,
recommended, or suggested in labeling covered by such approved application (except with
respect to such use, or conditions of use, as are the subject of an amendment or supplement
to such approved application, which amendment or supplement has been approved after the
enactment date under section 505 of the basic Act as amended by this Act) until whichever of
the following first occurs: (i) the expiration of the two-year period beginning with the enactment
date; (ii) the effective date of an order under section 505(e) of the basic Act, other than clause
(3) of the first sentence of such section 505(e), withdrawing or suspending the approval of
such application.
(4) In the case of any drug which, on the day immediately preceding the enactment date, (A)
was commercially used or sold inthe United States, (B) was not a new drug as defined by
section 201(p) of the basic Act as then in force, and (C) was not covered by an effective
application under section 505 of that Act, the amendments to section 201(p) made by this Act
shall not apply to such drug when intended solely for use under conditions prescribed,
recommended, or suggested in labeling with respect to such drug on that day.
1. Public Law 87–781, which was enacted October 10, 1962. The amendments made by such
Public Law to the Federal Food, Drug, and Cosmetic Act included amendments establishing
the requirement that new drugs be effective. Section 107(c) concerned the applicability of the
amendments.
PUBLIC LAW 88–136; REVOLVING FUND
TITLE II—DEPARTMENT OF HEALTH, EDUCATION, AND WELFARE
FOOD AND DRUG ADMINISTRATION
REVOLVING FUND FOR CERTIFICATION AND OTHER SERVICES 1
For the establishment of a revolving fund for certification and other services, there is hereby
appropriated the aggregate of fees (including advance deposits to cover such fees) paid
during the fiscal year 1964, and each succeeding fiscal year, for services in connection with
the listing, certification, or inspection of certain products and the establishment of tolerances
for pesticides, in accordance with sections 406, 408, 507, 702A, and 706 of the Federal Food,
Drug, and Cosmetic Act, as amended (21 U.S.C. 346a, 356, 357, 372a, and 376), and the
unexpended balance of such fees (or advance deposits) heretofore appropriated shall be
credited to such revolving fund. This fund shall be available without fiscal year limitation for
salaries and expenses necessary to carry out the Secretary’s responsibilities in connection
with such listings, certifications, inspections, or establishment of tolerances, including the
conduct of scientific research, development of methods of analysis, purchase of chemicals,
fixtures, furniture, and scientific equipment and apparatus; expenses of advisory committees;
refund of advance deposits for which no services have been rendered: Provided, That any
supplies, furniture, fixtures, and equipment on hand or on order on June 30, 1963, and
purchased or ordered under appropriations for "Salaries and Expenses, Certification,
Inspection, and Other Services," shall be used to capitalize the revolving fund.
1. The revolving fund provision is part of the Departments of Labor, and Health, Education,
and Welfare Appropriation Act, 1964.
SECTION 108 OF ANIMAL DRUG AMENDMENTS OF 1968 1
SEC . 108. (a) Except as otherwise provided in this section, the amendments made by the
foregoing sections shall take effect on the first day of the thirteenth calendar month which
begins after the date of enactment of this Act.
(b)(1) As used in this subsection, the term "effective date" means the effective date specified in
subsection (a) of this section; the term "basic Act" means the Federal Food, Drug, and
Cosmetic Act; and other terms used both in this section and the basic Act shall have the same
meaning as they have, or had, at the time referred to in the context, under the basic Act.
(2) Any approval, prior to the effective date, of a new animal drug or of an animal feed bearing
or containing a new animal drug, whether granted by approval of a new-drug application,
master file, antibiotic regulation, or food additive regulation, shall continue in effect, and shall
be subject to change in accordance with the provisions of the basic Act as amended by this
Act.
(3) In the case of any drug (other than a drug subject to section512(n) of the basic Act as
amended by this Act) intended for use n animals other than man which, on October 9, 1962, (A)
was commercially used or sold in the United States, (B) was not a new drug as defined by
section 201(p) of the basic Act as then in force, and(C) was not covered by an effective
application under section 505of that Act, the words "effectiveness" and "effective" contained in
section 201(v) to the basic Act shall not apply to such drug when intended solely for use under
conditions prescribed, recommended, or suggested in labeling with respect to such drug on
that day.
(4) Regulations providing for fees (and advance deposits to cover fees) which on the day
preceding the effective date applicable under subsection (a) of this section were in effect
pursuant to section507 of the basic Act shall, except as the Secretary may otherwise prescribe,
be deemed to apply also under section 512(n) of the basic Act, and appropriations of fees (and
of advance deposits to cover fees) available for the purposes specified in such section 507as
in effect prior to the effective date shall also be available for the purposes specified in section
512(n), including preparatory work or proceedings prior to that date
1. Public Law 90–399, which was enacted July 13, 1968 . Such Public Law added section
512to the Federal Food, Drug, and Cosmetic Act, and made related amendments. Section 108
concerned the effective date and applicability of the amendments.
SECTION 5 OF ORPHAN DRUG ACT 1
GRANTS AND CONTRACTS FOR DEVELOPMENT OF DRUGS FOR RARE DISEASES
AND CONDITIONS
SEC . 5. (a) [21 U.S.C. 360ee ] The Secretary may make grants to and enter into contracts
with public and private entities and individuals to assist in (1) defraying the costs of qualified
testing expenses incurred in connection with the development of drugs for rare diseases and
conditions, (2) defraying the costs of developing medical devices for rare diseases or
conditions, and (3) defraying the costs of developing medical foods for rare diseases or
conditions.
(b) For purposes of subsection (a):
(1) The term "qualified testing" means—
(A) human clinical testing—
(i) which is carried out under an exemption for a drug for a rare disease or condition under
section505(i) of the Federal Food, Drug, and Cosmetic Act (or regulations issued under such
section); and
(ii) which occurs after the date such drug is designated under section 526 of such Act and
before the date on which an application with respect to such drug is submitted under section
505(b) of such Act or under section 351 of the Public Health Service Act; and
(B) preclinical testing involving a drug for a rare disease or condition which occurs after the
date such drug is designated under section 526 of such Act and before the date on which an
application with respect to such drug is submitted under section 505(b) of such Act or under
section351 of the Public Health Service Act.
(2) The term "rare disease or condition" means (1) 2 in the case of a drug, any disease or
condition which (A) 2 affects less than 200,000 persons in the United States, or (B) 2 affects
more than 200,000 in the United States and for which there is no reasonable expectation that
the cost of developing and making available in the United States a drug for such disease or
condition will be recovered from sales in the United States of such drugs, (2) 2 in the case of a
medical device, any disease or condition that occurs so infrequently in the United States that
there is no reasonable expectation that a medical device for such disease or condition will be
developed without assistance under subsection (a), and (3) 2 in the case of a medical food,
any disease or condition that occurs so infrequently in the United States that there is no
reasonable expectation that a medical food for such disease or condition will be developed
without assistance under subsection (a). Determinations under the preceding sentence with
respect to any drug shall be made on the basis of the facts and circumstances as of the date
the request for designation of the drug under section 526 of the Federal Food, Drug, and
Cosmetic Act is made.
(3) The term "medical food" means a food which is formulated to be consumed or administered
enterally under the supervision of a physician and which is intended for the specific dietary
management of a disease or condition for which distinctive nutritional requirements, based on
recognized scientific principles, are established by medical evaluation.
(c) For grants and contracts under subsection (a), there are authorized to be appropriated
such sums as already have been appropriated for fiscal year 2002, and $25,000,000 for each
of the fiscal years 2003 through 2006.
1. Public Law 97–414.
2. So in law. See section 3 of Public Law 100–290 (102 Stat. 90). In subsection (b)(2) above,
the organizational units (1), (2), and (3) probably should be (A), (B), and (C) (and in the unit (1),
(A) and (B) probably should be (i) and (ii)).
Section Number Reference:
Federal Food, Drug, and
Cosmetic Act • Chapter I: Short Title
• Chapter II: Definitions
• Chapter III: Prohibited Acts and Penalties
• Chapter IV: Food
• Chapter V: Drugs and Devices
• Chapter VI: Cosmetics
• Chapter VII: General Authority
• Chapter VIII: Imports and Exports
• Chapter IX: Miscellaneous
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
Chapter I (U.S.C. Subchapter
I)--
Short Title 1 301
Chapter II (U.S.C. Subchapter
II)--
Definitions 201 321
Chapter III (U.S.C. Subchapter
III)--Prohibited Acts and
Penalties
Prohibited Acts 301 331
Injunction Proceedings 302 332
Penalties 303 333
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
Seizure 304 334
Hearing Before Report of
Criminal Violation
305 335
Debarment, Temporary Denial
of Approval, and Suspension
306 335a
Civil Penalties 307 335b
Authority to Withdraw Approval
of Abbreviated Drug
Applications
308 335c
Report of Minor Violations 309 336
Proceedings in Name of United
States; Provision as to
Subpoenas
310 337
Chapter IV (U.S.C.
Subchapter IV)--Food
Definitions and Standards for
Food
401 341
Adulterated Food 402 342
Misbranded Food 403 343
Enacted without a section
heading.
403A 343--1
Dietary Supplement Labeling
Exemptions
403B 343--2
Disclosure 403C 343--3
Emergency Permit Control 404 344
Regulations Making
Exemptions
405 345
Tolerances for Poisonous 406 346
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
Ingredients in Food
Oleomargarine or Margarine 407 347
Tolerances and Exemptions for
Pesticide Chemical Residues
408 346a
Food Additives 409 348
Bottled Drinking Water
Standards
410 349
Vitamins and Minerals 411 350
Requirements for Infant
Formulas
412 350a
New Dietary Ingredients 413 350b
Maintenance and Inspection of
Records
414 350c
Registration of Food Facilities 415 350d
Chapter V (U.S.C. Subchapter
V)--Drugs and Devices
Subchapter A (U.S.C. Part A)--
Drugs and Devices
Adulterated Drugs and Devices 501 351
Misbranded Drugs and Devices 502 352
Exemptions and Consideration
for Certain Drugs, Devices, and
Biological Products
503 353
Pharmacy Compounding 503A 353a
Veterinary Feed Directive Drugs 504 354
New Drugs 505 355
Pediatric Studies of Drugs 505A 355a
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
Research Into Pediatric Uses
for Drugs and Biological
Products
505B 355c
Fast Track Products 506 356
Manufacturing Changes 506A 356a
Reports of Postmarketing
Studies
506B 356b
Discontinuance of a Life Saving
Product
506C 356c
Repealed 507 357
Authority to Designate Official
Names
508 358
Nonapplicability to Cosmetics 509 359
Registration of Producers of
Drugs and Devices
510 360
Repealed 511 360a
New Animal Drugs 512 360b
Classification of Devices
Intended for Human Use
513 360c
Performance Standards 514 360d
Premarket Approval 515 360e
Banned Devices 516 360f
Judicial Review 517 360g
Notification and Other
Remedies
518 360h
Records and Reports on
Devices
519 360i
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
General Provisions Respecting
Control of Devices Intended for
Human Use
520 360j
State and Local Requirements
Respecting Devices
521 360k
Postmarket Surveillance 522 360l
Accredited Persons 523 360m
Subchapter B (U.S.C. Part
B)--Drugs for Rare Diseases or
Conditions
Recommendations for
Investigations of Drugs for Rare
Diseases and Conditions
525 360aa
Designation of Drugs for Rare
Diseases or Conditions
526 360bb
Protection for Drugs for Rare
Diseases or Conditions
527 360cc
Open Protocols for
Investigations of Drugs for Rare
Diseases or Conditions
528 360dd
Subchapter C (U.S.C. Part
C)—Electronic Product
Radiation Control
Definitions 531 360hh
Electronic Product Radiation
Control Program
532 360ii
Studies by the Secretary 533 360jj
Performance Standards for
Electronic Products
534 360kk
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
Notification of Defects In, and
Repair or Replacement Of,
Electronic Products
535 360ll
Imports 536 360mm
Inspection and Reports 537 360nn
Prohibited Acts 538 360oo
Enforcement 539 360pp
Repealed 540 360qq
Federal-State Cooperation 541 360rr
Effect on State Standards 542 360ss
Subchapter D (U.S.C. Part
D)—Dissemination of
Treatment Information
Requirements for Dissemination
of Treatment Information on
Drugs or Devices
551 360aaa
Information Authorized to be
Disseminated
552 360aaa-1
Establishment of List of Articles
and Publications Disseminated
and List of Providers That
Received Articles and
Reference Publications
553 360aaa-2
Requirement Regarding
Submission of Supplemental
Application for New Use;
Exemption from Requirement
554 360aaa-3
Corrective Actions; Cessation of
Dissemination
555 360aaa-4
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
Definitions 556 360aaa-5
Rules of Construction 557 360aaa-6
Subchapter E (U.S.C. Part
E)—General Provisions
Relating to Drugs and Devices
Expanded Access to
Unapproved Therapies and
Diagnostics
561 360bbb
Dispute Resolution 562 360bbb-1
Classification of Products 563 360bbb-2
Authorization for Medical
Products for Use in
Emergencies
564 360bbb-3
Subchapter F (U.S.C. Part
F)—New Animal Drugs for
Minor Use and Minor Species
Conditional Approval of New
Animal Drugs for Minor Use and
Minor Species
571 360ccc
Index of Legally Marketed
Unapproved New Animal Drugs
for Minor Species
572 360ccc-1
Designated New Animal Drugs
for Minor Use or Minor Species
573 360ccc-2
Chapter VI (U.S.C.
Subchapter VI)—Cosmetics
Adulterated Cosmetics 601 361
Misbranded Cosmetics 602 362
Regulations Making 603 363
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
Exemptions
Chapter VII (U.S.C.
Subchapter VII)—General
Authority
Subchapter A (U.S.C. Part
A)—General Administrative
Provisions
Regulations and Hearings 701 371
Examinations and
Investigations
702 372
Records of Interstate Shipment 703 373
Factory Inspection 704 374
Publicity 705 375
Seafood Inspection 706 376
Advertising of Certain Foods 707 378
Confidential Information 708 379
Presumption 709 379a
Consolidated Administrative
and Laboratory Facility
710 379b
Automation of Food and Drug
Administration
711 379d
Subchapter B (U.S.C. Part
B)—Colors
Listing and Certification of Color
Additives for Foods, Drugs, and
Cosmetics
721 379e
Subchapter C (U.S.C. Part
C)—Fees
Part 1 (U.S.C. Subpart
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
1)—Freedom of Information
Fees
Recovery and Retention of
Fees for Freedom of
Information Requests
731 379f
Part 2 (U.S.C. Subpart
2)—Fees Relating to Drugs
Definitions 735 379g
Authority to Assess and Use
Drug Fees
736 379h
Part 3 (U.S.C. Subpart
3)—Fees Relating to Devices
Definitions 737 379i
Authority to Assess and Use
Device Fees
738 379j
Part 4 (U.S.C. Subpart
4)—Fees Relating to Animal
Drugs
Definitions 739 379j-11
Authority to Assess and Use
Animal Drug Fees
740 379j-12
Subchapter D (Part
D)—Information and Education
Information System 741 379k
Education 742 379l
Subchapter E (U.S.C. Part
E)—Environmental Impact
Review
Environmental Impact 746 379o
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
Subchapter F (U.S.C. Part
F)—National Uniformity for
Nonprescription Drugs and
Preemption for Labeling or
Packaging of Cosmetics
National Uniformity for
Nonprescription Drugs
751 379r
Preemption for Labeling or
Packaging of Cosmetics
752 379s
Subchapter G (U.S.C. Part
G)—Safety Reports
Safety Report Disclaimers 756 379v
Chapter VIII (U.S.C.
Subchapter VIII)—Imports
and Exports
Imports and Exports 801 381
Exports of Certain Unapproved
Products
802 382
Office of International Relations 803 383
Importation of Prescription
Drugs
804 384
Chapter IX (U.S.C.
Subchapter
IX)—Miscellaneous
Separability Clause 901 391
Effective Date and Repeals 902 392
Food and Drug Administration 903 393
Scientific Review Groups 904 394
Loan Repayment Program 905 395
Cross-reference of Section Numbers: FD&C Act and United States Code
Section Title FD&C Act Number U.S. Code Section Number
(21 U.S.C)
Practice of Medicine 906 396
Contracts for Expert Review 907 396
Notices to States Regarding
Imported Food
908 398
Grants to States for Inspections 909 399