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Transition from CSV to CSA; FDA Final CSA Guidance, September 2025 for Medical Device Manufacturing & Quality Testing

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

Best Practices in Preparation for an FDA Computer System Audit in 2025

Best Practices in Preparation for an FDA Computer System Audit in 2025

Overview: In 2025, the FDA's expectations for validated computer systems have never been high..

Date : 31st July 2025

Time : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

Storytelling in Project Management for Validating FDA-Regulated Computer Systems: How to Captivate & Inspire the Team

Storytelling in Project Management for Validating FDA-Regulated Computer Systems: How to Captivate & Inspire the Team

Overview: Validating FDA-regulated (“GxP”) computer systems often stalls for reasons that have..

Date : 25th February 2026

Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time

Duration : 90 Mins

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