In Vitro Diagnostic Regulation (IVDR) - Technical documentation & Post-Market Surveillance (PMS)

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Registration for the webinar

Currently there are no future dates for the webinar.

Speaker & Moderator

Moderator 1 of the webinar: <p>Thomas Fritzsch</p>

Thomas Fritzsch

Main speaker

Moderator 2 of the webinar: <p>Nina Marx</p>

Nina Marx

Moderator

Webinar information

Part 2 – IVDR Technical documentation & Post-Market Surveillance (PMS)

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.


📅 Date & Time: April 30, 2026 – 10:00–11:00 CEST (Berlin) / 9:00–10:00 BST (UK)

✅Duration: 60 minutes (until 11:00 AM)

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