Key Considerations in Verification & Validation of Medical Devices
Website http://www.onlinecompliancepanel.com/webinar/MEDICAL-DEVICE-VALIDATION-501081/DEC-2015-ES-OURGLOCAL |
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Category Verification, validation, FDA, 483, software validation, process validation, design verification and design validation, validation training, FDA 483 observations, 21 CFR ยง 820.30, how to avoid FDA 483s, CMMi Requirements Management, Verification & Validation testing
Deadline: December 15, 2015 | Date: December 16, 2015
Venue/Country: Online Event, U.S.A
Updated: 2015-11-25 21:22:28 (GMT+9)
Call For Papers - CFP
This webinar will cite what are the key considerations in medical device design and validation that can help prevent FDA 483s.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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