FDA is the federal agency responsible for ensuring that foods are safe, wholesome and sanitary; human and veterinary drugs, biological products, and medical devices are safe and effective; cosmetics are safe; and electronic products that emit radiation are safe. FDA also ensures that these products are honestly, accurately and informatively represented to the public. Some of the agency's specific responsibilities include: Biologics, Cosmetics, Drugs, Foods, Medical Devices, Radiation Emitting Electronic Products, Veterinary Products and in relation to paper it regulates the ability of paper stocks to be used in the above areas.
ood and rug dministration - government agency charged with controlling the safety of foods and drugs. Has come under fire for biased enforcement favoring drugs over nutrients
Food and Drugs Administration (US government agency)
The FDA is an agency of the U.S. Department of Health and Human Services that regulates the testing of experimental drugs and medical products. Using evidence of safety, efficacy or equivalence, the FDA approves and regulates the marketing of medical products.
Government public health organization regulating drugs, biological products, medical devices, food supply, cosmetics, and products that emit radiation.
Food and Drug Administrators (USA).
A U.S. government agency responsible for ensuring that foods derived from new plant varieties are safe to eat. FDA also has legal authority for food labeling.
The Food & Drug Administration is the US Federal agency responsible for the regulation of biotechnology food products.
Is a scientific, regulatory and public health agency. Its jurisdiction encompasses most food products, human and animal drugs, medical devices, radiation emmitting products and cosmetics for human use
U.S. Food & Drug Administration http://www.fda.gov
Food and Drug Administration.
An organization that sets standards and regulations for the packaging of food.
The federal government organization that is responsible for public safety with regard to foods and beverages, pharmaceuticals, and to some extent medical and healthcare devices.
Food & Drug Administration; US Federal Government agency responsible for the regulation of both Rx and OTC medicines.
The U.S. government agency that (1) enforces laws on the manufacturing, tests, and use of drugs and medical devices and (2) approves a new drug or device before it is made available to the public.
An acronym for the Food and docug Administration. This federal agency is responsible for determining the validity and safety of any docug, cosmetic, medical device or medical procedure.
A United States government body that oversees medical devices, including contact lenses, intraocular lenses, excimer lasers and eye drops. In the U.S., these products must be approved by the FDA before they can be marketed.
(Food & Drug Administration) - It is the US federal agency responsible for the regulation of pharmaceuticals (drugs) and food products
A part of the Department of Health and Human Services’ Public Health Service that is responsible for ensuring the safety and wholesomeness of all foods processed and sol in interstate commerce except meat, poultry and eggs. The FDA also inspects food plants and imported foods and sets standards for food composition.
An United States government agency with authority over certain processes and products within the U.S. healthcare and food markets.
(United States) Food & Drug Administration
Food & Drug Administration of the United States Department of Health and Human Services.
Federal Drug Administration
US Federal agency responsible for safety and regulation of foods and pharmaceutical products.
is the United States Food & Drug Administration, an agency of the US government.
the federal agency responsible for regulating the development, use and safety of drugs, medical devices, food, cosmetics, and related products
The FDA is an agency of the U.S. Department of Health and Human Services that ensures the safety and efficacy of drugs and medical devices by regulating their availability or distribution. Using evidence of safety, efficacy, or equivalence as established in clinical trials and studies, the FDA approves the market release of medical devices and drugs.
nbspFood and Drug Administration. Regulations for PS applications apply to the following area: Adhesives: (1) Direct food contact, such as labelling of fruit and vegetable with an edible skin (175.125); (2) Indirect food contact, where incidental between an