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.
§ 346a - Tolerances and exemptions for pesticide chemical residues
§ 346 - Tolerances for poisonous or deleterious substances in food; regulations
§ 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§ 357 - Repealed.
§ 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
§ 216 - Regulations
§ 263b - Certification of mammography facilities
42 USC § 259 to 261a - Repealed.