§ 351. Adulterated drugs and devices

§ 352. Misbranded drugs and devices

§ 353. Exemptions and consideration for certain drugs, devices, and biological products

§ 353a. Pharmacy compounding

§ 354. Veterinary feed directive drugs

§ 355. New drugs

§ 355a. Pediatric studies of drugs

§ 355b. Adverse-event reporting

§ 355c. Research into pediatric uses for drugs and biological products

§ 356. Fast track products

§ 356-1. Accelerated approval of priority countermeasures

§ 356a. Manufacturing changes

§ 356b. Reports of postmarketing studies

§ 356c. Discontinuance of life saving product

§ 357. Repealed.]

§ 358. Authority to designate official names

§ 359. Nonapplicability of subchapter to cosmetics

§ 360. Registration of producers of drugs or devices

§ 360a. Repealed.]

§ 360b. New animal drugs

§ 360c. Classification of devices intended for human use

§ 360d. Performance standards

§ 360e. Premarket approval

§ 360f. Banned devices

§ 360g. Judicial review

§ 360h. Notification and other remedies

§ 360i. Records and reports on devices

§ 360j. General provisions respecting control of devices intended for human use

§ 360k. State and local requirements respecting devices

§ 360l. Postmarket surveillance

§ 360m. Accredited persons