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Part 2 – IVDR Technical documentation & Post-Market Surveillance (PMS)
Date & Time: April 30, 2026 | 10:00 AM
Duration: 60 minutes (until 11:00 AM)

This webinar covers the requirements for technical documentation and post-market surveillance in accordance with IVDR. Using typical weak points as examples, it explains how documents must be structured and PMS processes integrated.

Register now for part 2 of the webinar series free of charge!

Part 3 – IVDR Performance evaluation
Date & Time: May 21, 2026 | 10:00 AM
Duration: 60 minutes (until 11:00 AM)

The focus is on the requirements for performance evaluation according to IVDR, including scientific validity as well as analytical and clinical performance data.

Register now for part 3 of the webinar series free of charge!

Part 4 – IVDR Performance studies
Date & Time: June 3, 2026 | 10:00 AM
Duration: 60 minutes (until 11:00 AM)

This webinar addresses IVDR performance study requirements from planning to Notified Body assessment.

Register now for part 4 of the webinar series free of charge!