food and drug administration
- Guideline or reference source
- ClinicalTrials.gov Glossary of common site terms
- Definition
- An agency within the U.S. Department of Health and Human Services. FDA is responsible for protecting the public health by making sure that human and veterinary drugs, vaccines and other biological products, medical devices, the nation's food supply, cosmetics, dietary supplements, and products that give off radiation are safe, effective, and secure.
- Abbreviation for
- FDA
- Broader Term
- regulatory authority
- Narrower Term
- center for biologics evaluation and research
- center for devices and radiologic health
- center for drug evaluation and research
- Related Term
- European Medicines Agency
- health canada
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