Public health effectiveness of the FDA 510(k) clearance process : balancing patient safety and innovation : workshop report / Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) clearance process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies.

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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Bibliographic Details
Corporate Authors: Institute of Medicine (U.S.). Board on Population Health and Public Health Practice (Author), Institute of Medicine (U.S.). Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process (Author)
Other Authors: Wizemann, Theresa M.
Format: Electronic eBook
Language:English
Published: Washington, D.C. : National Academies Press, [2010], ©2010.
Series:Online access: NCBI NCBI Bookshelf.
Subjects:
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
United States
Congress
proceedings (reports)
Conference papers and proceedings.
Online Access: Full text (Wentworth users only)
Local Note:ProQuest Ebook Central

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