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Webinar: Clinical evaluation according to MDR

Important information: Webinar series completed

We would like to inform you that the webinar series “Clinical evaluation according to MDR” has now concluded.
If you have any questions or would like to learn more about our services, contact us now because our team is always here to assist you.

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Step by step to MDR-compliant clinical evaluation!


A clinical evaluation is one of the core elements of MDR certification, but it poses major challenges for many manufacturers. Our free, four-part webinar series offers a clear, practical overview of the methodology for preparing a clinical evaluation according to MDR requirements.

We will be focusing on the following:

  • Key areas of assessment, typical pitfalls, and common non-conformities
  • Regulatory and clinical requirements for clinical data
  • Supplementing the clinical evaluation with post-market follow-up activities
  • Specific references to relevant sections of the MDR and MDCG guidelines

Part 1 – Fundamentals before starting the clinical evaluation
Date & Time: September 11, 2025 | 10:00 AM
Duration: 45 minutes (ends at 10:45 AM)

This webinar provides a comprehensive overview of the MDR and its various conformity assessment procedures. We will explain how products are qualified and classified, as well as the specific features that manufacturers need to consider. This event is particularly aimed at manufacturers who have not yet undergone MDR certification, as well as international participants. The webinar lays the fundamental groundwork on which the clinical evaluation is based.

Part 2 – Planning and literature research
Date & Time: October 09, 2025 | 10:00 AM
Duration: 60 minutes (ends at 11:00 AM)

This webinar offers insights from a clinical expert on how to structure a clinical evaluation effectively from the beginning.
You will also receive tips on systematic literature research.

Part 3 – Appraisal and analysis of clinical data
New date & Time: November 06, 2025 | 10:00 AM
Duration: 60 minutes (ends at 11:00 AM)

The third part of the webinar covers the appraisal and statistical analysis of clinical data. We also explain the function and requirements of clinical trials.

Part 4 – Clinical data as proof of conformity
Date & Time: November 27, 2025 | 10:00 AM
Duration: 60 minutes (ends at 11:00 AM)

In the final webinar, you will learn how to use clinical data to demonstrate safety and performance requirements (GSPR 1 and 8).
We will also explain the role of PMS and PMCF data in clinical evaluations.

The webinar series is complete!

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