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Best Practices in Preparation for an FDA Computer System Audit
Overview: FDA requires that all computer systems used to produce, manage and report on “GxP” (G..
Date : 30th September 2021
Time : This Event is Over and the Recorded Copy is Available
Duration : 1 Hour 55 Mins
21 CFR Part 820 - Quality System - Principles of Lean Documents and Lean Configuration
Overview: All life science businesses are required to maintain their Quality Management Syste..
Date : 21st September 2021
Time : This Event is Over and the Recorded Copy is Available
Duration : 1 Hour 30 Mins
Best Practices in Preparation for an FDA Computer System Audit - What You Need to Know?
Overview: FDA requires that all computer systems used to produce, manage and report on “GxP” ..
Date : 29th July 2021
Time : This Event is Over and the Recorded Copy is Available
Duration : 1 Hour 40 Mins
In-Depth Testing of Computer Systems Regulated by FDA - What You Need to Know?
Overview:This webinar will focus on testing as a key element of Computer System Validation (CSV). ..
Date : 28th May 2021
Time : This Event is Over and the Recorded Copy is Available
Duration : 1 Hour 24 Mins
Data Integrity and Governance for Computer Systems Regulated by FDA - What to Know
Overview:The Webinar will focus on the importance of ensuring that the validation of an FDA-regula..
Date : 24th March 2021
Time : This Event is Over and the Recorded Copy is Available
Duration : 1 Hour 46 Mins