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Public Health Effectiveness Of The Fda 510k Clearance Process Balancing Patient Safety And Innovation Workshop Report 1st Edition Institute Of Medicine Board On Population Health And Public Health Practice Committee On The Public Health Effectiveness Of The Fda 510k Clearance Process Theresa Wizemann

Name: Public Health Effectiveness Of The Fda 510k Clearance Process Balancing Patient Safety And Innovation Workshop Report 1st Edition Institute Of Medicine Board On Population Health And Public Health Practice Committee On The Public Health Effectiveness Of The Fda 510k Clearance Process Theresa Wizemann
SKU: BELL-51400174
Price: 31.00 USD
Availability: InStock
Rating: 4.7 (96 reviews)

SKU: BELL-51400174

Public Health Effectiveness Of The Fda 510k Clearance Process Balancing Patient Safety And Innovation Workshop Report 1st Edition Institute Of Medicine Board On Population Health And Public Health Practice Committee On The Public Health Effectiveness Of The Fda 510k Clearance Process Theresa Wizemann

$ 31.00 ~~$ 45.00~~ (-31%)

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96 reviews

Public Health Effectiveness Of The Fda 510k Clearance Process Balancing Patient Safety And Innovation Workshop Report 1st Edition Institute Of Medicine Board On Population Health And Public Health Practice Committee On The Public Health Effectiveness Of The Fda 510k Clearance Process Theresa Wizemann instant download after payment.

Publisher: National Academies Press

File Extension: PDF

File size: 2.96 MB

Pages: 140

Author: Institute of Medicine; Board on Population Health and Public Health Practice; Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process; Theresa Wizemann

ISBN: 9780309158503, 0309158508

Language: English

Year: 2010

Edition: 1

Product desciption

Public Health Effectiveness Of The Fda 510k Clearance Process Balancing Patient Safety And Innovation Workshop Report 1st Edition Institute Of Medicine Board On Population Health And Public Health Practice Committee On The Public Health Effectiveness Of The Fda 510k Clearance Process Theresa Wizemann by Institute Of Medicine; Board On Population Health And Public Health Practice; Committee On The Public Health Effectiveness Of The Fda 510(k) Clearance Process; Theresa Wizemann 9780309158503, 0309158508 instant download after payment.

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 balance patient safety and technological innovation. This document summarizes the workshop.