There is a newer version of the US Code
2011 US Code
Title 21 - Food and Drugs
Chapter 9 - FEDERAL FOOD, DRUG, AND COSMETIC ACT (§§ 301 - 399d)
Subchapter V - DRUGS AND DEVICES (§§ 351 - 360ccc-2)
Part A - Drugs and Devices (§§ 351 - 360n)
View MetadataMetadata
Publication Title | United States Code, 2006 Edition, Supplement 5, Title 21 - FOOD AND DRUGS |
Category | Bills and Statutes |
Collection | United States Code |
SuDoc Class Number | Y 1.2/5: |
Contained Within | Title 21 - FOOD AND DRUGS CHAPTER 9 - FEDERAL FOOD, DRUG, AND COSMETIC ACT SUBCHAPTER V - DRUGS AND DEVICES Part A - Drugs and Devices |
Contains | sections 351 to 360n |
Date | 2011 |
Laws in Effect as of Date | January 3, 2012 |
Positive Law | No |
Disposition | standard |
- Section 351 - Adulterated drugs and devices
- Section 352 - Misbranded drugs and devices
- Section 353 - Exemptions and consideration for certain drugs, devices, and biological products
- Section 353a - Pharmacy compounding
- Section 353b - Prereview of television advertisements
- Section 354 - Veterinary feed directive drugs
- Section 355 - New drugs
- Section 355-1 - Risk evaluation and mitigation strategies
- Section 355a - Pediatric studies of drugs
- Section 355b - Adverse-event reporting
- Section 355c - Research into pediatric uses for drugs and biological products
- Section 355d - Internal committee for review of pediatric plans, assessments, deferrals, and waivers
- Section 355e - Pharmaceutical security
- Section 356 - Fast track products
- Section 356-1 - Accelerated approval of priority countermeasures
- Section 356a - Manufacturing changes
- Section 356b - Reports of postmarketing studies
- Section 356c - Discontinuance of life saving product
- Section 357 - Repealed. Pub. L. 105-115, title I, ยง125(b)(1), Nov. 21, 1997, 111 Stat. 2325
- Section 358 - Authority to designate official names
- Section 359 - Nonapplicability of subchapter to cosmetics
- Section 360 - Registration of producers of drugs or devices
- Section 360a - Clinical trial guidance for antibiotic drugs
- Section 360b - New animal drugs
- Section 360c - Classification of devices intended for human use
- Section 360d - Performance standards
- Section 360e - Premarket approval
- Section 360e-1 - Pediatric uses of devices
- Section 360f - Banned devices
- Section 360g - Judicial review
- Section 360h - Notification and other remedies
- Section 360i - Records and reports on devices
- Section 360j - General provisions respecting control of devices intended for human use
- Section 360k - State and local requirements respecting devices
- Section 360l - Postmarket surveillance
- Section 360m - Accredited persons
- Section 360n - Priority review to encourage treatments for tropical diseases
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