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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

Functional and System Requirements for Systems Regulated by FDA in 2024

Functional and System Requirements for Systems Regulated by FDA in 2024

Overview: The validation of computer systems (CSV) under FDA regulations has shaped the way e..

Date : 25th November 2024

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 2024

Best Practices in Preparation for an FDA Computer System Audit in 2024

10 Minutes excerpt from the recorded event for your review: Best Practices in Preparation for a..

Date : 22nd July 2024

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

Duration : 90 Mins

Computer Software Assurance: Risk-Based Validation With Time-Saving Templates

Computer Software Assurance: Risk-Based Validation With Time-Saving Templates

Overview:This webinar describes exactly what is required for compliance with Part 11 and the Europe..

Date : 30th January 2023

Time : This Event is Over

Duration : 90 Mins

Best Practices for FDA Computer System Audit Preparation in 2026

Best Practices for FDA Computer System Audit Preparation in 2026

Overview: For those of us who have worked around FDA-regulated computer systems for many year..

Date : 29th May 2026

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

Duration : 90 Mins

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