URI(s)
- http://id.loc.gov/authorities/subjects/sh2014001248
- http://id.loc.gov/authorities/sh2014001248#concept
Variants
- Drugs--Registration
- Registration of drugs
Broader Terms
Closely Matching Concepts from Other Schemes
Sources
- found: Work cat: Moropa. M. A retrospective analysis of applications submitted to the Medicines Control Council of South Africa for the registration as antiretrovirals, 2013.
- found: Merck web site, May 15, 2014(Merck is committed to pursuing rapid registration of our antiretrovirals (ARVs), including in those countries most affected by HIV/AIDS)
- found: U.S. Food and Drud Administration web site, May 15, 2014:Drugs sub page (Regulatory Guidance Drug Registration and Listing: Section 510 of the Federal Food, Drug, and Cosmetic Act requires manufacturers, repackers, and relabelers that engage in the manufacture, preparation, propagation, compounding, or processing of human or veterinary drugs and human biological products to register their establishment(s) and submit a listing of every product in commercial distribution with the FDA. This information helps FDA maintain a catalog of all human and veterinary drugs and biologics in commercial distribution in the United States)
Instance Of
Scheme Membership(s)
Collection Membership(s)
Change Notes
- 2014-05-15: new
- 2014-08-12: revised
Alternate Formats