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Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR-
Overview: In today's rapidly evolving life sciences landscape, ensuring data integrity and pr..
Date : 21st March 2024
Time : This Event is Over
Duration : 90 Mins
510K Submission Process for Medical Devices
Overview: There are three types of 510(k) submissions that can be submitted – Traditional, Spec..
Date : 25th August 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Medical Device Software Validation Meeting FDA Regulations
Overview: Testing software to prove that it works and has no bugs is not sufficient to obtain ..
Date : 25th October 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 75 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