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21 CFR 3 - PRODUCT JURISDICTION

Authority: 21 U.S.C. 321, 351, 353, 355, 360, 360c-360f, 360h-360j, 360gg-360s s, 360bbb-2, 371(a), 379e, 381, 394; 42 U.S.C. 216, 262, 264.
Source: 56 FR 58756, Nov. 21, 1991, unless otherwise noted.

Title 21 published on 2012-04-01

no entries appear in the Federal Register after this date.

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.


United States Code
USC : Title 21 - FOOD AND DRUGS

§ 221 to 237 - Repealed. July 1, 1944, ch. 373, title XIII,

§ 301 - Short title

§ 321d - Market names for catfish and ginseng

§ 321c - Nonfat dry milk; “milk” defined

§ 321b - “Package” defined

§ 321a - “Butter” defined

§ 321 - Definitions; generally

§ 331 - Prohibited acts

§ 332 - Injunction proceedings

§ 333a - Repealed.

§ 333 - Penalties

§ 334 - Seizure

§ 335b - Civil penalties

§ 335a - Debarment, temporary denial of approval, and suspension

§ 335 - Hearing before report of criminal violation

§ 335c - Authority to withdraw approval of abbreviated drug applications

§ 336 - Report of minor violations

§ 337 - Proceedings in name of United States; provision as to subpoenas

§ 341 - Definitions and standards for food

§ 342 - Adulterated food

§ 343a - Repealed.

21 USC § 343–3 - Disclosure

21 USC § 343–2 - Dietary supplement labeling exemptions

21 USC § 343–1 - National uniform nutrition labeling

§ 343 - Misbranded food

§ 344 - Emergency permit control

§ 345 - Regulations making exemptions

§ 346b - Authorization of appropriations

§ 346a - Tolerances and exemptions for pesticide chemical residues

§ 346 - Tolerances for poisonous or deleterious substances in food; regulations

§ 347b - Contravention of State laws

§ 347a - Congressional declaration of policy regarding oleomargarine sales

§ 347 - Intrastate sales of colored oleomargarine

§ 348 - Food additives

§ 349 - Bottled drinking water standards; publication in Federal Register

§ 350e - Sanitary transportation practices

§ 350d - Registration of food facilities

§ 350c - Maintenance and inspection of records

§ 350b - New dietary ingredients

§ 350a - Infant formulas

§ 350 - Vitamins and minerals

§ 350g - Hazard analysis and risk-based preventive controls

§ 350f - Reportable food registry

21 USC § -

21 USC § -

§ 350k - Laboratory accreditation for analyses of foods

§ 350j - Targeting of inspection resources for domestic facilities, foreign facilities, and ports of entry; annual report

§ 350i - Protection against intentional adulteration

§ 350h - Standards for produce safety

§ 351 - Adulterated drugs and devices

§ 352 - Misbranded drugs and devices

§ 353b - Prereview of television advertisements

§ 353a - Pharmacy compounding

§ 353 - Exemptions and consideration for certain drugs, devices, and biological products

§ 354 - Veterinary feed directive drugs

§ 355e - Pharmaceutical security

§ 355d - Internal committee for review of pediatric plans, assessments, deferrals, and waivers

§ 355c - Research into pediatric uses for drugs and biological products

§ 355b - Adverse-event reporting

§ 355a - Pediatric studies of drugs

21 USC § 355–1 - Risk evaluation and mitigation strategies

§ 355 - New drugs

§ 356c - Discontinuance of life saving product

§ 356b - Reports of postmarketing studies

§ 356a - Manufacturing changes

21 USC § 356–1 - Accelerated approval of priority countermeasures

§ 356 - Fast track products

§ 357 - Repealed.

§ 358 - Authority to designate official names

§ 359 - Nonapplicability of subchapter to cosmetics

§ 360 - Registration of producers of drugs or devices

§ 360n - Priority review to encourage treatments for tropical diseases

§ 360m - Accredited persons

21 USC § -

§ 360k - State and local requirements respecting devices

§ 360j - General provisions respecting control of devices intended for human use

§ 360i - Records and reports on devices

§ 360h - Notification and other remedies

§ 360g - Judicial review

§ 360f - Banned devices

21 USC § 360e–1 - Pediatric uses of devices

§ 360e - Premarket approval

§ 360d - Performance standards

§ 360c - Classification of devices intended for human use

§ 360b - New animal drugs

§ 360a - Clinical trial guidance for antibiotic drugs

§ 360ee - Grants and contracts for development of drugs for rare diseases and conditions

§ 360dd - Open protocols for investigations of drugs for rare diseases or conditions

§ 360cc - Protection for drugs for rare diseases or conditions

§ 360bb - Designation of drugs for rare diseases or conditions

§ 360aa - Recommendations for investigations of drugs for rare diseases or conditions

21 USC § -

§ 360kk - Performance standards for electronic products

§ 360jj - Studies by Secretary

§ 360ii - Program of control

§ 360hh - Definitions

§ 360ss - State standards

§ 360rr - Federal-State cooperation

§ 360qq - Repealed.

§ 360pp - Enforcement

21 USC § -

§ 360nn - Inspection, records, and reports

§ 360mm - Imports

21 USC § 360bbb–2 - Classification of products

21 USC § 221 to 237 - Repealed. July 1, 1944, ch. 373, title XIII,

§ 371 - Regulations and hearings

§ 379e - Listing and certification of color additives for foods, drugs, devices, and cosmetics

§ 381 - Imports and exports

§ 394 - Scientific review groups

U.S.C. : Title 42 - THE PUBLIC HEALTH AND WELFARE

§ 216 - Regulations

§ 262 - Regulation of biological products

§ 264 - Regulations to control communicable diseases