Website http://www.onlinecompliancepanel.com/webinar/MEDICAL-DEVICE-VALIDATION-501081/DEC-2015-ES-OURGLOCAL | Edit Freely
Category Verification, validation, FDA, 483, software validation, process validation, design verification and design validation, validation training, FDA 483 observations, 21 CFR § 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)
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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