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CFR › Title 21 › Chapter I › Subchapter A › Part 26

21 CFR 26 - MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STATES AND THE EUROPEAN COMMUNITY

Title 21 published on 2011-04-01

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

15 USC 1453 - Requirements of labeling; placement, form, and contents of statement of quantity; supplemental statement of quantity

15 USC 1454 - Rules and regulations

15 USC 1455 - Procedure for promulgation of regulations

18 USC 1905 - Disclosure of confidential information generally

21 USC 321 - Definitions; generally

21 USC 331 - Prohibited acts

21 USC 351 - Adulterated drugs and devices

21 USC 352 - Misbranded drugs and devices

21 USC 355 - New drugs

21 USC 360 - Registration of producers of drugs or devices

21 USC 360b - New animal drugs

21 USC 360c - Classification of devices intended for human use

21 USC 360d - Performance standards

21 USC 360e - Premarket approval

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

21 USC 360f - Banned devices

21 USC 360g - Judicial review

21 USC 360h - Notification and other remedies

21 USC 360i - Records and reports on devices

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

21 USC § -

21 USC 360m - Accredited persons

21 USC 371 - Regulations and hearings

21 USC 374 - Inspection

21 USC 381 - Imports and exports

21 USC 382 - Exports of certain unapproved products

21 USC 383 - Office of International Relations

21 USC 393 - Food and Drug Administration

42 USC 216 - Regulations

42 USC 241 - Research and investigations generally

42 USC § -

42 USC 262 - Regulation of biological products

42 USC 264 - Regulations to control communicable diseases

42 USC 265 - Suspension of entries and imports from designated places to prevent spread of communicable diseases

5 USC 552 - Public information; agency rules, opinions, orders, records, and proceedings