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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
Audit Trail Review by Exception in FDA-Regulated Environments: Reducing Review Burden While Strengthening Data Integrity
Overview Audit trails are essential to maintaining trustworthy electronic records in FDA-regu..
Date : 28th August 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 90 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
Risk-Based Excel Spreadsheet Validation and FDA Compliance - Risk-Based CSV/CSA & Part 11
Overview:FDA inspections and audits continue to put a bright spotlight on data integrity—especiall..
Date : 27th January 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
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