FDA reform in Congress: interview with Peter Barton Hutt. Food and Drug Administration. Interview by John S. James.
AIDS Treat News
; (no 245): 4-5, 1996 Apr 19.
Article
en En
| MEDLINE
| ID: mdl-11363623
AIDS: Peter Barton Hutt, one of the world's leading experts on Food and Drug Administration (FDA) law, addresses issues concerning rapid approval for protease inhibitors, funding for development of AIDS drugs, and legislative processes impacting drug development. Hutt discusses the changes in the drug approval process. Over the last two decades the time it takes for a drug to go through the development to approval process has increased from 6 to 8 years to 15 to 16 years. This extension is not due to the approval process itself, but to the requirement for more research and development. Suggestions are made as to how to cut down approval time, and thus cut drug costs. Specific bills addressing drug approval are outlined and compared.^ieng
Buscar en Google
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Antivirales
/
Aprobación de Drogas
Tipo de estudio:
Prognostic_studies
/
Qualitative_research
Límite:
Humans
País/Región como asunto:
America do norte
Idioma:
En
Revista:
AIDS Treat News
Asunto de la revista:
SINDROME DA IMUNODEFICIENCIA ADQUIRIDA (AIDS)
Año:
1996
Tipo del documento:
Article