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  2. Title 21 of the Code of Federal Regulations - Wikipedia

    en.wikipedia.org/wiki/Title_21_of_the_Code_of...

    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). [1] It is divided into three chapters: Chapter I — Food and Drug Administration

  3. List of Schedule III controlled substances (U.S.) - Wikipedia

    en.wikipedia.org/wiki/List_of_Schedule_III...

    This is the list of Schedule III controlled substances in the United States as defined in section 202 of the Controlled Substances Act (21 U.S.C. § 812) and 21 CFR 1308.13. The following findings are required for substances to be placed in this schedule:

  4. Title 21 of the United States Code - Wikipedia

    en.wikipedia.org/wiki/Title_21_of_the_United...

    21 U.S.C. ch. 25 — Miscellaneous Anti-Drug Abuse Provisions; See also. Title 21 of the Code of Federal Regulations – Food and Drugs; References ...

  5. Drug-eluting stent - Wikipedia

    en.wikipedia.org/wiki/Drug-eluting_stent

    The FDA approval process for DES involves submitting an investigational device exemption (IDE) application to conduct clinical trials under 21 CFR Part 812, and then a premarket approval (PMA) application to obtain marketing authorization under 21 CFR Part 8144.

  6. List of Schedule V controlled substances (U.S.) - Wikipedia

    en.wikipedia.org/wiki/List_of_Schedule_V...

    This is the list of Schedule V controlled substances in the United States as defined by the Controlled Substances Act. [1] The following findings are required for substances to be placed in this schedule: [2]

  7. Code of Federal Regulations - Wikipedia

    en.wikipedia.org/wiki/Code_of_Federal_Regulations

    "About Code of Federal Regulations". Government Publishing Office. 9 March 2017. "A Research Guide to the Federal Register and the Code of Federal Regulations". Law Librarians' Society of Washington, D.C. July 21, 2012. "Report to Congress on the Costs and Benefits of Federal Regulations". Office of Management and Budget. September 30, 1997.

  8. Federal Food, Drug, and Cosmetic Act of 1938 - Wikipedia

    en.wikipedia.org/wiki/Federal_Food,_Drug,_and...

    As codified in 21 U.S.C. chapter 9 of the United States Code from the LII; As codified in 21 U.S.C. chapter 9 of the United States Code from the US House of Representatives; Federal Food, Drug, and Cosmetic Act (PDF/details) as amended in the GPO Statute Compilations collection; Color Additive Status List; Food Ingredients and Colors

  9. Federal Tort Claims Act - Wikipedia

    en.wikipedia.org/wiki/Federal_Tort_Claims_Act

    The Federal Tort Claims Act (August 2, 1946, ch. 646, Title IV, 60 Stat. 812, 28 U.S.C. Part VI, Chapter 171 and 28 U.S.C. § 1346) ("FTCA") is a 1946 federal statute that permits private parties to sue the United States in a federal court for most torts committed by persons acting on behalf of the United States.