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Transition from CSV to CSA; FDA Final CSA Guidance, September 2025 for Medical Device Manufacturing & Quality Testing
Overview: For decades, life-science teams have relied on Computer System Validation (CSV)—sha..
Date : 21st November 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
21 CFR Part 11: FDA Expectations for Electronic Records & Electronic Signatures in Modern Systems
Overview: As regulated companies accelerate digital transformation—moving quality, laboratory..
Date : 12th March 2026
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 90 Mins
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