Learn how to assess existing evidence, identify testing gaps and plan an MRI safety assessment that supports your intended labelling claims and target markets.
Why attend this webinar?
Supporting or extending an MRI safety claim involves complex testing and regulatory decisions. Manufacturers need to determine whether existing evidence remains valid, how product changes affect previous claims and when additional testing is required.
This webinar will provide practical guidance on MRI testing, evidence planning and documentation. It will help manufacturers identify evidence gaps and develop an appropriate strategy for their devices, product families and target markets.
Webinar details
- Date: 29th October 2026
- Pick a timing that suits you best:
- 10AM CET (5PM SGT/5AM EDT)
- 3PM CET (10PM SGT/10AM EDT)
- Duration: 60 minutes, including live Q&A
- Format: Live webinar
What you will learn
- When existing MRI data can be used vs. when new testing is required
- How design and manufacturing changes impact MRI safety claims
- Practical ways to extend MRI labeling (e.g., 1.5T to 3T)
- How to reduce testing using worst-case and device-family approaches
- How to align with FDA, MDR, and global requirements
- How to streamline testing, simulation, and documentation
- What are special considerations for your device (5-minute quick checkups)
- How TÜV SÜD can support your MRI strategy
Thomas Eigentler, Dr.-Ing.
Global Business Development Expert and Senior Product Specialist MRI Safety, TÜV SÜD
