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...
Clasificación: | Libro Electrónico |
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Autores Corporativos: | , |
Otros Autores: | |
Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
Washington, D.C. :
National Academies Press,
[2010], ©2010.
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Colección: | Online access: NCBI NCBI Bookshelf.
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Temas: | |
Acceso en línea: | Texto completo |
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