There Is a Newer Version of the U.S. Code
2008 U.S. Code
Title 21 - FOOD AND DRUGS
CHAPTER 9 - FEDERAL FOOD, DRUG, AND COSMETIC ACT
SUBCHAPTER V - DRUGS AND DEVICES
Part A - Drugs and Devices
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| Publication Title | United States Code, 2006 Edition, Supplement 2, 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 | 2008 |
| Laws in Effect as of Date | January 5, 2009 |
| 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. 353b - 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. 355d - Internal committee for review of pediatric plans, assessments, deferrals, and waivers
- Sec. 355e - Pharmaceutical security
- Sec. 356 - Fast track products
- Sec. 356-1 - Accelerated approval of priority countermeasures
- Sec. 356a - Manufacturing changes
- Sec. 356b - Reports of postmarketing studies
- Sec. 356c - Discontinuance of life saving product
- Sec. 357 - Repealed.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. 360b - New animal drugs
- Sec. 360c - Classification of devices intended for human use
- Sec. 360d - Performance standards
- Sec. 360e - Premarket approval
- Sec. 360e-1 - Pediatric uses of devices
- Sec. 360f - Banned devices
- Sec. 360g - Judicial review
- Sec. 360h - Notification and other remedies
- 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
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