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  1. Title 21 of the United States Code governs Food and Drugs in the United States Code (U.S.C.).

  2. The United States Code (formally the Code of Laws of the United States of America) is the official codification of the general and permanent federal statutes of the United States. It contains 53 titles (Titles 1–54, excepting Title 53, which is reserved for a proposed title on small business ).

  3. Title 21 of the CFR is reserved for rules of the Food and Drug Administration. Each title (or volume) of the CFR is revised once each calendar year.

  4. Title 21 of the U.S. Code covers various topics related to food, drugs, cosmetics, and alcohol. It includes chapters on adulterated or misbranded products, narcotics, pharmacy, pesticides, biomaterials, and more.

  5. The Federal Food, Drug, and Cosmetic Act (FD&C Act) is the main law enforced by the U.S. Food and Drug Administration. It is codified into Title 21 Chapter 9 of the United States Code, which can be searched on the Law Revision Counsel website.