Drug Efficacy Study Implementation (DESI) was a program begun by the Food and Drug Administration (FDA) in the 1960s after the requirement (in the Kefauver-Harris Drug Control Act) that all drugs be efficacious as well as safe, was made part of US law. The DESI program was intended to classify all pre-1962 drugs that were already on the market as either effective, ineffective, or needing further study. The Drug Efficacy Study Implementation (DESI) evaluated over 3,000 separate products and over 16,000 therapeutic claims. By 1984, final action had been completed on 3,443 products; of these, 2,225 were found to be effective, 1,051 were found not effective, and 167 were pending.
One of the early effects of the DESI study was the development of the Abbreviated New Drug Application (ANDA).
See also
- Estes Kefauver
- Federal Food, Drug, and Cosmetic Act
- Inverse benefit law
- Regulation of therapeutic goods
References
- Pharmacy Today. August 2008. FDA aims to remove unapproved drugs from market: Risk-based enforcement program focuses on removing potentially harmful products
External links
- National Academies of Sciences archives. The Drug Efficacy Study of the National Research Council’s Division of Medical Sciences, 1966-1969
- Chhabra R, Kremzner ME, Kiliany BJ. FDA policy on unapproved drug products: past, present, and future. Ann Pharmacother. 2005 Jul-Aug;39(7-8):1260-4. PMID 15956239
This article incorporates public domain material from websites or documents of the United States Department of Health and Human Services.
.svg){kind=small} | This United States government–related article is a stub. You can help Misplaced Pages by expanding it. |