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21 CFR Part 11 & Data Integrity 2026: CSA, Cloud, AI & Annex 11
OverviewA Part 11 problem rarely begins with someone deliberately ignoring a regulation. More ofte..
Date : 23rd September 2026
Time : This Event is Over
Duration : 75 Mins
The 6 Most Common Problems in FDA Software Validation and Verification in 2026
Overview: Software validation and verification remain common sources of compliance risk for F..
Date : 14th May 2026
Time : This Event is Over
Duration : 75 Mins
Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2026
Overview: In 2026, data integrity and privacy risks don’t sit in one department—they show up ..
Date : 19th March 2026
Time : This Event is Over
Duration : 90 Mins
The 6 Most Common Problems in FDA Software Validation and Verification in 2025
Overview: Professionals working with FDA-regulated software face numerous challenges when it co..
Date : 12th June 2025
Time : This Event is Over
Duration : 75 Mins
The 6 Most Common FDA Software Validation Failures and How to Prevent Them
Overview: One of the most concerning findings during an FDA inspection is discovering that an ..
Date : 10th November 2026
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 75 Mins