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21 CFR Part 11 Compliance for Computer Systems Regulated by FDA


The seminar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. This includes development of a company philosophy and approach, and incorporating it into the overall Computer System Validation program and plans for individual systems that have this capability.
Event link : https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901789SEMINAR?upcomingevents-sep-seo

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