ENTITY
U.S. Department of Health and Human Services, Food and Drug Administration
1 document
351 definitions

Document NameDate

21 C.F.R. § 1.227
11 definitions

2013-04-01

Controlled Substances Act
48 definitions

1970-10-27

Drugs@FDA Glossary of Terms
39 definitions

2012-02-02

EVM Glossary of Terms
50 definitions

2013-07-30

FDA-TRACK Research Glossary
76 definitions

2015-04-28

Food Code
42 definitions

2009-01-01

Food Labeling
37 definitions

2008-04-01

Guidance for Industry
9 definitions

2008-04-01

Pulmonary-Allergy Drugs Advisory Committee on the safety of long-acting beta-agonist bronchodilators
3 definitions

2005-06-09

Quality System Regulation
25 definitions

2013-04-01

Requirements for Specific Standardized Food Dressings and Flavorings
11 definitions

2014-04-01
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About
FDA is responsible for protecting the public health by assuring the safety, efficacy and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation. FDA is also responsible for advancing the public health by helping to speed innovations that make medicines more effective, safer, and more affordable and by helping the public get the accurate, science-based information they need to use medicines and foods to maintain and improve their health. FDA also has responsibility for regulating the manufacturing, marketing and distribution of tobacco products to protect the public health and to reduce tobacco use by minors. Finally, FDA plays a significant role in the Nation’s counterterrorism capability. FDA fulfills this responsibility by ensuring the security of the food supply and by fostering development of medical products to respond to deliberate and naturally emerging public health threats.