food and drug administration

Food and Drug Administration. A division of the U.S. Public Health Service in the Department of Health and Human Services responsible for ensuring that food is safe, pure, and wholesome; that human and animal drugs, biological products, and medical devices are safe and effective; and that certain other products, such as electronic products that emit radiation, are safe. • Created by the Pure Food and Drug Act of 1906, the agency today enforces the Food, Drug, and Cosmetic Act of 1938 and related statutes and regulations. 21USCA §§ 301 et seq. — Abbr. FDA.

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词条贡献者

译者Lorna，毕业于国内一流的法学院，擅长翻译各种与商业秘密相关的法律文件。