Using EU GMP Annex 22 as the Framework for Governing AI Systems, Validation Traceability, and Data Integrity Controls
Learn how to apply EU GMP Annex 22 as a practical framework for AI system governance, validation traceability, lifecycle management, and data integrity controls in regulated pharmaceutical and biotech environments.
Instructor
Charles H. Paul
President, CHP Consulting LLC — Regulatory Compliance & Operational Excellence
What You'll Learn
About This Event
Curriculum
Requirements
- Working in EU GMP-regulated pharmaceutical, biotechnology, medical device, or advanced therapy environments
- Applicable to QA, validation, IT, digital transformation, regulatory affairs, and compliance professionals
Who Should Attend
Quality Assurance Directors, Quality Systems Managers, GMP Compliance Professionals, Validation Managers, Computer System Validation Specialists, Digital Transformation Leaders, Manufacturing Directors, Operations Directors, Regulatory Affairs Professionals, Data Integrity Specialists, IT Quality Managers, Automation Engineers, Quality Risk Management Leaders, Internal Auditors, AI Governance Teams, Compliance Consultants, and Executive Leadership Teams.
Areas Covered
Meet Your Instructor

Charles H. Paul
President, CHP Consulting LLC — Regulatory Compliance & Operational Excellence
Charles H. Paul is President of CHP Consulting LLC, a regulatory compliance, operational excellence, training, and technical documentation consulting firm supporting pharmaceutical, biotechnology, medical device, and advanced therapy organizations worldwide. With more than 30 years of experience in regulated manufacturing environments, Charles specializes in helping organizations build sustainable quality systems that support compliance, operational performance, workforce effectiveness, and inspection readiness.
Event Details
Format
Live Webinar
Duration
1 hour
Certificate
Included
Date
Monday, August 24, 2026
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