What is Food and Drug Administration?

  • (noun): A federal agency in the Department of Health and Human Services established to regulate the release of new foods and health-related products.
    Synonyms: FDA

Food And Drug Administration

The Food and Drug Administration (FDA or USFDA) is an agency of the United States Department of Health and Human Services, one of the United States federal executive departments. The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), and veterinary products. The FDA also enforces other laws, notably Section 361 of the Public Health Service Act and associated regulations, many of which are not directly related to food or drugs. These include sanitation requirements on interstate travel and control of disease on products ranging from certain household pets to sperm donation for assisted reproduction.

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Some articles on Food and Drug Administration:

Food And Drug Administration, Maharashtra State
... Food and Drug Administration, Maharashtra State, is Maharashtra's primary instrument of consumer protection ... of Maharashtra entrusted the responsibility of enforcement of the Prevention of Food Adulteration Act, 1954 to FDA which is when it got its present name ...
List Of Clinical Research Topics - Government Agencies - Food and Drug Administration - Review and Approval Programs
... to collect safety and effectiveness data Investigational New Drug – allows an investigational drug to be used in a clinical study in order to collect safety and ...
Patient Safety Organization - Governmental Organizations - United States - Food and Drug Administration
... The Food and Drug Administration is an agency of the United States government that regulates food, drugs, medical devices and biological products for human use ... The FDA receives medication error reports on marketed human drugs from direct contacts and manufacturer's reports, and in 1992, began monitoring medication error reports that are forwarded from the United States ... The effectiveness of the FDA's drug safety monitoring procedures was called into question after several approved drugs were shown to have serious side-effects ...
Naval Ordnance Laboratory - Food and Drug Administration
... The Food and Drug Administration (FDA), part of the US Department of Health and Human Services (HHS), decided to consolidate offices from various locations in the suburban ...

Famous quotes containing the words food and/or drug:

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