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U.S. Food and Drug Administration (FDA) Introduction
Release Date: [2017/3/30 15:33:12]    Total read [] Times

      U.S. Food and Drug Administration (Food and Drug Admistraton referred to as FDA), under the U.S. Department of Health Education and Welfare, responsible for the national pharmaceutical, food, biological products, cosmetics, veterinary drugs, medical devices and diagnostic supplies management. FDA under the Drug Administration, Food Administration, Veterinary Bureau, Bureau of Radiological Health, Bureau of biological products, medical devices and diagnostic supplies Bureau and the National Toxicology Centre, the regional task management, namely the six Board (some publications, also known as 6 centers), a center and a regional management organization. U.S. Food and Drug Administration agency currently employs about 7,500 people, FDA headquarters 1143, including Drug Administration for the 350.

    Medicines Agency (also known as Center for Drug Evaluation and Research) is responsible for the work of drug approval for human use, with eight offices and a number of departments.

1. Drug Administration. Under the drug information, information systems design, administration and budget, Medical Library 4 sections.

2. Drug Administration Office. Under a drug quality assessment, supervision and drug label, production and product quality, scientific research and investigation, and regulations 7 departments.

3. Drug Standards Division. With commonly used drugs assessment, drug marketing and advertising, two families.

4. A drug review. Under the cardiovascular - renal medicine, anti-tumor

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