Difference between revisions of "Food and Drug Administration"
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The FDA is one of the four regulatory members of the [[International Conference on Harmonisation]] ([[ICH]]), along with the [[European Medicines Agency]] ([[EMEA]]), the [[European Commission]] and the Japanese [[Ministry of Health, Labor and Welfare]] ([[MHLW]]). | The FDA is one of the four regulatory members of the [[International Conference on Harmonisation]] ([[ICH]]), along with the [[European Medicines Agency]] ([[EMEA]]), the [[European Commission]] and the Japanese [[Ministry of Health, Labor and Welfare]] ([[MHLW]]). | ||
| − | FDA is the sponsor of the [[HL7]] [[ | + | FDA is the sponsor of the [[HL7]] [[Regulated Product Submissions]] Project. |
==Food and Drug Administration Organization== | ==Food and Drug Administration Organization== | ||
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===Center for Drugs Evaluation and Review (CDER)=== | ===Center for Drugs Evaluation and Review (CDER)=== | ||
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===Center for Biologics Evaluation and Review (CBER)=== | ===Center for Biologics Evaluation and Review (CBER)=== | ||
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===Center for Food Safety and Applied Nutrition (CFSAN)=== | ===Center for Food Safety and Applied Nutrition (CFSAN)=== | ||
| − | + | This branch regulates food, dietary supplements, food additives, and cosmetics. From the viewpoint of the [[RPS]] project, the areas of most concern are food additives and cosmetics, which require regulatory approval to be marketed. | |
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| + | Information on the current process of electronic submissions of Food and Color Additives to CFSAN can be found on the FDA website: [http://www.cfsan.fda.gov/~dms/opaegui2.html], and uses form [http://www.cfsan.fda.gov/~acrobat/frm3503.pdf FDA Form 3503] for Food Additives and [http://www.cfsan.fda.gov/~acrobat/frm3504.pdf FDA Form 3504] for Color Additives. | ||
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| + | There are no current procedures for electronic filing of Dietary Supplements, Food Labeling or Cosmetics. All CFSAN guidance can be found here: [http://www.cfsan.fda.gov/~dms/guidance.html] | ||
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===Center for Veterinary Medicine (CVM)=== | ===Center for Veterinary Medicine (CVM)=== | ||
| − | { | + | {{sectstub}} |
===Center for Devices and Radiological Health (CDRH)=== | ===Center for Devices and Radiological Health (CDRH)=== | ||
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===National Center for Toxicological Research (NCTR)=== | ===National Center for Toxicological Research (NCTR)=== | ||
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===Office of Regulatory Affairs (ORA)=== | ===Office of Regulatory Affairs (ORA)=== | ||
| − | { | + | {{sectstub}} |
==External Links== | ==External Links== | ||
*[http://www.fda.gov Food and Drug Administration Home Page] | *[http://www.fda.gov Food and Drug Administration Home Page] | ||
*[http://en.wikipedia.org/wiki/Food_and_drug_administration Wikipedia page on Food and Drug Administration] | *[http://en.wikipedia.org/wiki/Food_and_drug_administration Wikipedia page on Food and Drug Administration] | ||
| + | *[http://www.infosafe.fr/Armoirefortedin/Armoirefortedin.htm Armoire forte de sécurité] | ||
[[Category:RPS Glossary]] | [[Category:RPS Glossary]] | ||
Latest revision as of 16:04, 18 April 2016
This is a Glossary page for the RPS Project
The U.S. Food and Drug Administration (FDA) is the United States Regulatory Authority that controls the manufacture, quality and distribution of drugs, biological medical products, medical devices, foods, dietary supplements, vaccines, blood products, veterinary products and cosmetics. It is a division of the U.S. Department of Health and Human Services.
The FDA is one of the four regulatory members of the International Conference on Harmonisation (ICH), along with the European Medicines Agency (EMEA), the European Commission and the Japanese Ministry of Health, Labor and Welfare (MHLW).
FDA is the sponsor of the HL7 Regulated Product Submissions Project.
Contents
- 1 Food and Drug Administration Organization
- 1.1 The Office of the Commissioner
- 1.2 Center for Drugs Evaluation and Review (CDER)
- 1.3 Center for Biologics Evaluation and Review (CBER)
- 1.4 Center for Food Safety and Applied Nutrition (CFSAN)
- 1.5 Center for Veterinary Medicine (CVM)
- 1.6 Center for Devices and Radiological Health (CDRH)
- 1.7 National Center for Toxicological Research (NCTR)
- 1.8 Office of Regulatory Affairs (ORA)
- 2 External Links
Food and Drug Administration Organization
The U.S. FDA consists of the following major subdivisions:
The Office of the Commissioner
The commissioner is a presidential appointment. Currently, the commissioner is Andrew von Eschenbach.
Center for Drugs Evaluation and Review (CDER)
Center for Biologics Evaluation and Review (CBER)
Center for Food Safety and Applied Nutrition (CFSAN)
This branch regulates food, dietary supplements, food additives, and cosmetics. From the viewpoint of the RPS project, the areas of most concern are food additives and cosmetics, which require regulatory approval to be marketed.
Information on the current process of electronic submissions of Food and Color Additives to CFSAN can be found on the FDA website: [1], and uses form FDA Form 3503 for Food Additives and FDA Form 3504 for Color Additives.
There are no current procedures for electronic filing of Dietary Supplements, Food Labeling or Cosmetics. All CFSAN guidance can be found here: [2]
