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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. National Donor Deferral Registry - Wikipedia

    en.wikipedia.org/wiki/National_Donor_Deferral...

    The National Donor Deferral Registry, also known as the (NDDR) is a database of individuals who have tested "reactive" for viral agents like human immunodeficiency viruses (HIV), Hepatitis B virus (HBV), and hepatitis C virus (HCV) and are permanently prohibited from donating plasma. [1]

  4. Title 21 CFR Part 11 - Wikipedia

    en.wikipedia.org/wiki/Title_21_CFR_Part_11

    Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered trustworthy, reliable, and equivalent to paper records (Title 21 CFR Part 11 Section 11.1 (a)).

  5. Title 21 of the United States Code - Wikipedia

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

    21 U.S.C. ch. 18 — Presidents Media Commission on Alcohol and Drug Abuse Prevention 21 U.S.C. ch. 19 — Pesticide Monitoring Improvements 21 U.S.C. ch. 20 — National Drug Control Program

  6. Code of Federal Regulations - Wikipedia

    en.wikipedia.org/wiki/Code_of_Federal_Regulations

    A few volumes of the CFR at a law library (titles 12–26) 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 ...

  7. FDA citizen petition - Wikipedia

    en.wikipedia.org/wiki/FDA_citizen_petition

    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]

  8. Generally recognized as safe - Wikipedia

    en.wikipedia.org/wiki/Generally_recognized_as_safe

    The Code of Federal Regulations, revised as of April 1, 2020, [7] includes (CFR) title 21 170.30(b) that provides general recognition of safety through scientific procedures requires the same quantity and quality of scientific evidence needed to obtain approval of the substance as a food additive.

  9. Federal Register - Wikipedia

    en.wikipedia.org/wiki/Federal_Register

    In addition to purchasing printed copies or subscriptions, the contents of the Federal Register can be acquired via several commercial databases: Citation Technologies offers the complete Federal Register and Code of Federal Regulations (CFRs) through subscription-based web portals such as CyberRegs. [13]