Webinar: Stay Ahead of EU GMP Annex 11 – What to Focus on Today
Register Now
The revision of Annex 11 is no longer a future topic – it is becoming reality and it will significantly impact how computerized systems in regulated environments are managed, validated, and inspected. Many organizations are currently trying to understand what these changes mean in practice and whether their existing setups will still meet regulatory expectations once the updated requirements are fully in force.
In this complimentary webinar, Julia Gatzka, Teamlead Validation Services at EXTEDO, breaks down what is really changing in Annex 11 – and what it means for your systems, processes, and responsibilities. Rather than focusing on theory, the session will translate regulatory language into practical implications for your day-to-day work with validated systems.
Date: 30 April 2026
Time: 16:00 CEST / 10:00 EDT
Not sure if you can join in live? Just register to receive the recording!
Register now to explore the following topics with us:
- Background of Annex 11 & timeline
- Content Comparison of the effective version and the revised draft
- Deep dives into significant topics
- EXTEDO recommendations for proactive preparation
This session is built to leave you with a clear sense of direction, reduce uncertainty, and provide clarity in a regulatory environment that is clearly evolving. You will understand which areas typically require action, where organizations most often underestimate risk, and how you can start preparing in a structured and realistic way.
Use this chance you assess your current state more confidently and identify the steps that matter most going forward!