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21 U.S.C. ch. 6 — [Narcotic Drugs] (repealed or transferred) 21 U.S.C. ch. 7 — Practice of Pharmacy and Sale of Poisons in Consular Districts in China; 21 U.S.C. ch. 8 — Narcotic Farms (repealed) 21 U.S.C. ch. 9 — Federal Food, Drug, and Cosmetic Act; 21 U.S.C. ch. 10 — Poultry and Poultry Products Inspection Poultry Products ...
Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP).
Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES).
Title 20: Education Title 21: Food and Drugs: Title 22: Foreign Relations and Intercourse Title 23: Highways 1958 Title 24: Hospitals and Asylums: Title 25: Indians: Title 26: Internal Revenue Code: Title 27: Intoxicating Liquors: Title 28: Judiciary and Judicial Procedure: 1948 Title 29: Labor Title 30: Mineral Lands and Mining: Title 31 ...
Title 21 of the United States Code; Title 22 of the United States Code; Title 23 of the United States Code; Title 24 of the United States Code; Title 25 of the United ...
In the law of the United States, the Code of Federal Regulations (CFR) is the codification of the general and permanent regulations promulgated by the executive departments and agencies of the federal government of the United States. The CFR is divided into 50 titles that represent broad areas subject to federal regulation.
It is described in Title 21 of the Code of Federal Regulations (21 CFR Part 10). Pharmaceutical companies routinely use FDA citizen petitions to delay the entry of generic drugs into the United States marketplace. [1]
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