Public Health Effectiveness of the FDA 510(K) Clearance Process: Measuring Postmarket Performance and Other Select Topics - Workshop Report
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- Synopsis
- The Food and Drug Administration (FDA) is responsible for ensuring that medical devices are safe and effective before they go on the market. As part of its assessment of the FDA's premarket clearance process for medical devices, the IOM held a workshop on July 28 to discuss how medical devices are monitored for safety after they are available to consumers. This document summarizes the workshop.
- Copyright:
- 2011
Book Details
- Book Quality:
- Publisher Quality
- ISBN-13:
- 9780309162067
- Publisher:
- National Academies Press
- Date of Addition:
- 07/14/12
- Copyrighted By:
- the National Academy of Sciences.
- Adult content:
- No
- Language:
- English
- Has Image Descriptions:
- No
- Categories:
- Nonfiction, Medicine
- Submitted By:
- Bookshare Staff
- Usage Restrictions:
- This is a copyrighted book.