Public health effectiveness of the FDA 510(k) clearance process : measuring postmarket performance and other select topics : workshop report /

Mostrar otras versiones (2)

"The Food and Drug Administration (FDA) is responsible for ensuring that medical devices are safe and effective before they go on the market. Section 510(k) of the Federal Food, Drug, and Cosmetic Act requires a manufacturer of medical devices to notify FDA of its intent to market a medical dev...

Descripción completa

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor Corporativo: Institute of Medicine (U.S.). Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process
Otros Autores: Wizemann, Theresa M.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Washington, D.C. : National Academies Press, ©2011.
Temas:
United States. > Food and Drug Administration > Congresses.
United States > Food and Drug Administration
United States. > Food and Drug Administration
Public health > Equipment and supplies > Standards > United States > Congresses.
Public health > United States > Congresses.
Device Approval > standards
Device Approval > legislation & jurisprudence
Equipment Safety > standards
Santé publique > États-Unis > Congrès.
HEALTH & FITNESS > Safety.
Public health
United States
Congress
Electronic resource.
proceedings (reports)
Conference papers and proceedings
Conference papers and proceedings.
Actes de congrès.
Acceso en línea:Texto completo

Ejemplares similares

Ejemplares similares