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2015 US Code
Title 21 - Food and Drugs (Sections 1 - 2252)
Chapter 9 - Federal Food, Drug, and Cosmetic Act (Sections 301 - 399f)
Subchapter V - Drugs and Devices (Sections 351 - 360fff-7)
Part A - Drugs and Devices (Sections 351 - 360n-1)
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Metadata
Publication Title | United States Code, 2012 Edition, Supplement 3, 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-1 |
Date | 2015 |
Laws In Effect As Of Date | January 3, 2016 |
Positive Law | No |
Disposition | standard |
- Sec. 351 - Adulterated drugs and devices
- Sec. 352 - Misbranded drugs and devices
- Sec. 353 - Exemptions and consideration for certain drugs, devices, and biological products
- Sec. 353a - Pharmacy compounding
- Sec. 353a-1 - Enhanced communication
- Sec. 353b - Outsourcing facilities
- Sec. 353c - Prereview of television advertisements
- Sec. 354 - Veterinary feed directive drugs
- Sec. 355 - New drugs
- Sec. 355-1 - Risk evaluation and mitigation strategies
- Sec. 355a - Pediatric studies of drugs
- Sec. 355b - Adverse-event reporting
- Sec. 355c - Research into pediatric uses for drugs and biological products
- Sec. 355c-1 - Report
- Sec. 355d - Internal committee for review of pediatric plans, assessments, deferrals, deferral extensions, and waivers
- Sec. 355e - Pharmaceutical security
- Sec. 355f - Extension of exclusivity period for new qualified infectious disease products
- Sec. 356 - Expedited approval of drugs for serious or life-threatening diseases or conditions
- Sec. 356-1 - Accelerated approval of priority countermeasures
- Sec. 356a - Manufacturing changes
- Sec. 356b - Reports of postmarketing studies
- Sec. 356c - Discontinuance or interruption in the production of life-saving drugs
- Sec. 356c-1 - Annual reporting on drug shortages
- Sec. 356d - Coordination; task force and strategic plan
- Sec. 356e - Drug shortage list
- Sec. 356f - Hospital repackaging of drugs in shortage
- Sec. 357 - Repealed. Pub. L. 105-115, title I, ยง125(b)(1), Nov. 21, 1997, 111 Stat. 2325
- Sec. 358 - Authority to designate official names
- Sec. 359 - Nonapplicability of subchapter to cosmetics
- Sec. 360 - Registration of producers of drugs or devices
- Sec. 360a - Clinical trial guidance for antibiotic drugs
- Sec. 360a-1 - Clinical trials
- Sec. 360b - New animal drugs
- Sec. 360c - Classification of devices intended for human use
- Sec. 360c-1 - Reporting
- Sec. 360d - Performance standards
- Sec. 360e - Premarket approval
- Sec. 360e-1 - Pediatric uses of devices
- Sec. 360f - Banned devices
- Sec. 360g - Judicial review
- Sec. 360g-1 - Agency documentation and review of significant decisions regarding devices
- Sec. 360h - Notification and other remedies
- Sec. 360h-1 - Program to improve the device recall system
- Sec. 360i - Records and reports on devices
- Sec. 360j - General provisions respecting control of devices intended for human use
- Sec. 360k - State and local requirements respecting devices
- Sec. 360l - Postmarket surveillance
- Sec. 360m - Accredited persons
- Sec. 360n - Priority review to encourage treatments for tropical diseases
- Sec. 360n-1 - Priority review for qualified infectious disease products
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