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CFR › Title 21 › Chapter I › Subchapter A › Part 58

21 CFR Part 58 - GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES

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

§ 342 - Adulterated food

§ 346a - Tolerances and exemptions for pesticide chemical residues

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

§ 348 - Food additives

§ 351 - Adulterated drugs and devices

§ 352 - Misbranded drugs and devices

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

§ 355 - New drugs

§ 360 - Registration of producers of drugs or devices

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

§ 360i - Records and reports on devices

§ 360h - Notification and other remedies

§ 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

§ 371 - Regulations and hearings

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

§ 381 - Imports and exports

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

§ 216 - Regulations

§ 263b - Certification of mammography facilities

42 USC § 259 to 261a - Repealed.