Validation for Medical Device and Diagnostic Manufacturers
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- Synopsis
- Implementation of FDA's Design Control requirements (21 CFR 820.30) changed an entire industry. Quality System Requirements defined the approach to medical device validation. Product design, manufacturing process, and test method validation studies must be performed before or as a product is transferred to commercial production. Validation studies
- Copyright:
- 2007
Book Details
- Book Quality:
- Publisher Quality
- ISBN-13:
- 9781040204382
- Related ISBNs:
- 9780429130410, 9781439810460, 9781574910636
- Publisher:
- CRC Press
- Date of Addition:
- 11/17/24
- Copyrighted By:
- Informa Healthcare USA, Inc.
- Adult content:
- No
- Language:
- English
- Has Image Descriptions:
- No
- Categories:
- Nonfiction, Science, Technology, Medicine
- Submitted By:
- Bookshare Staff
- Usage Restrictions:
- This is a copyrighted book.
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