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21 C.F.R. Part 329 – Nonprescription Human Drug Products Subject to Section 760 of the Federal Food, Drug, and Cosmetic Act | Midpage
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Code of Federal Regulations
Title 21
Chapter I
Subchapter D
Part 329
21 C.F.R. Part 329
Nonprescription Human Drug Products Subject to Section 760 of the Federal Food, Drug, and Cosmetic Act
329.100
Postmarketing reporting of adverse drug events under section 760 of the Federal Food, Drug, and Cosmetic Act.