This webinar will address the use of the FDA, GAMP, 21 CFR Part 11, "Electronic Records" / "Electronic Signatures", and other applicable industry software validation models, coupled with the ISO 14971 / ICH Q9 Product Risk Management models, to plan, structure, run, and document acceptable software validations.
Software Verification and Validation Planning and Documentation - Webinar By GlobalCompliancePanel
24 April 2013, Fremont, United States
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Online Training
Livermore Common, Online Training, California, Fremont, 94539, United States
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GlobalCompliancePanel
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