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
Introduction
Venue
Online Training
Livermore Common, Online Training, California, Fremont, 94539, United States
Useful links
Organised by
GlobalCompliancePanel
Contact information
Mr John Robinson
Livermore Common, Fremont, 94539, United States of America
8004479407
Contact us by email
Livermore Common, Fremont, 94539, United States of America
8004479407
Contact us by email
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