Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report /

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"The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balanc...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autores Corporativos: Institute of Medicine (U.S.). Board on Population Health and Public Health Practice (Autor), Institute of Medicine (U.S.). Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process (Autor)
Otros Autores: Wizemann, Theresa M.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Washington, D.C. : National Academies Press, [2010], ©2010.
Colección:Online access: NCBI NCBI Bookshelf.
Temas:
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.
MEDICAL > Family & General Practice.
MEDICAL > Osteopathy.
MEDICAL.
MEDICAL > Holistic Medicine.
HEALTH & FITNESS > Reference.
MEDICAL > Essays.
MEDICAL > Alternative Medicine.
HEALTH & FITNESS > Holism.
Public health
United States
Congress
proceedings (reports)
Conference papers and proceedings
Conference papers and proceedings.
Actes de congrès.
Acceso en línea:Texto completo

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