Semantic Scholar
Open Access
2020
740 sitasi
United States food and drug administration
C. Carey
Abstrak
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.
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C. Carey
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- Tahun Terbit
- 2020
- Bahasa
- en
- Total Sitasi
- 740×
- Sumber Database
- Semantic Scholar
- DOI
- 10.1016/b978-0-12-813467-2.00108-5
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- Open Access ✓