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

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

"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
Autor principal: Institute of Medicine (U.S.).
Autores Corporativos: Institute of Medicine (U.S.). Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process (-), Institute of Medicine (U.S.). Board on Population Health and Public Health Practice
Otros Autores: Wizemann, Theresa (-)
Formato: Libro electrónico
Idioma:Inglés
Publicado: Washington, D.C. : National Academies Press 2010.
Edición:1st ed
Materias:
United States. > Food and Drug Administration.
Public health > Standards > United States > Congresses.
Public health > United States > Congresses.
Ver en Biblioteca Universitat Ramon Llull:https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009622293806719

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