United States food and drug administration

By C. Carey. Clinical Engineering Handbook, 2020

747 citations recorded by the source corpus.

Abstract The US Food and Drug Administration (FDA) regulates medical devices primarily through the law known as the Federal Food, Drug, and Cosmetic Act, as Amended (“the FD&C Act,” or “the Act”). Regulations promulgated by FDA in Title 21 of the Code of Federal Regulations (CFR) spell out the broad provisions contained in the Act.

Subfields: Pediatrics, Perinatology and Child Health, Pharmacology, Public Health, Environmental and Occupational Health

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