Food and Drug Administration Agency

FDA (Food and Drug Administration)—agency administered under the U.S. Department of Health and Human Services (formerly Health, Education and Welfare) "to enforce the Federal Food, Drug, and Cosmetic Act and thereby carry out the purpose of Congress to insure that foods are safe, pure, and wholesome, and made under sanitary conditions drugs and therapeutic devices are safe and effective for their intended uses cosmetics are safe and prepared from appropriate ingredients and that all of these products are honestly and informatively labeled and packaged."... 

Food and Drug Administration Federal Food, Drug, and Cosmetic Act, Title 21 Environmental Protection Agency, Title 40... 

Food and Drug Administration Act officially establishes FDA as an agency of the Department of Health and Human Services with a Commissioner of Food and Drugs appointed by the President. 

Two forms of pegylated IFN-a have been approved by the Food and Drug Administration (FDA) and by the European Medicines Agency (EMEA) for the... 

The federal government develops regulations and recommendations to protect public health. Regulations can be enforced by law. Federal agencies that develop regulations for toxic substances include the Environmental Protection Agency (EPA), the Occupational Safety and Health Administration (OSHA), and the Food and Drug Administration (FDA). 

For pharmaceutical products, the synthesis route is usually established very early on because of drug registration procedures carried out with governmental agencies, e.g. the Food and Drug Administration (FDA). 

Because the conclusions that can be reached from an LSMBS depend critically on the choice of commodities, involvement of relevant regulatory agencies [e.g., EPA, USDA, and Food and Drug Administration (FDA)] in the USA, depending on the commodity and study objective] should be considered. Agreement on the choice of commodities by such authorities will ensure that the study and its outcome will be acceptable for regulatory purposes. 

FDA. 1998. Accidental radioactive contamination of human food and animal feed Recommendations for state and local agencies. U.S. Food and Drug Administration. 

Food and Drug Administration, Federal Security Agency, Trade Correspondence Letter 3-A... 

During the media blitz that followed, Patterson urged the public to buy Chicken of the Sea tuna because the Van Camp Sea Food Company s molded steel cans were lead-free. With characteristic bluntness, Patterson lambasted a host of government laboratories from the Environmental Protection Agency and its Bureau of Foods to the National Marine Fisheries Service and the Food and Drug Administration (FDA). Asked if any other laboratories agreed with his findings, Patterson declared loftily that scientific questions are not determined by majority vote. 

Act on the Evaluation of Chemical Substances and Regulation of Their Manufacture, etc. (Act No. 117 of October 16,1973 amended in 2009)], as well as their continued use by the U.S. Environmental Protection Agency (EPA) [Kavlock R, Dix D. J Toxicol Environ Health B Crit Rev 13(2-4) 197-217, 2010] and U.S. Food and Drug Administration (FDA) [U.S. Environmental Protection Agency (EPA) and U.S. Food and Drug Administration (FDA) TSCA (1976) Toxic Substances Control Act. United States Publ. Law 94-469, 90 Stat 2003, USA],... 

U.S. Environmental Protection Agency (EPA) and U.S. Food and Drug Administration (FDA) TSCA (1976) Toxic Substances Control Act. United States Publ. Law 94-469, 90 Stat 2003, USA... 

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