Join Our Webinar: How to trust AI enabled Medical Devices. An overview covering technical and clinical aspects.

Discover how the EU AI Act impacts the medical device industry and learn about the essential steps to navigate the regulatory landscape for AI-enabled medical devices. This exclusive webinar, with two different session times, will provide insights into:

  • Conformity assessment under the EU AI Act and MDR.
  • AI-enabled medical device testing: robustness, trustworthiness and cybersecurity.
  • Clinical evaluation best practices: leveraging MDCG 2020-01 and real-world data to ensure safety and performance.
  • Emerging standards and state-of-the-art testing methods for AI and machine learning technologies.
 
When?


  February 19th

  • 9 am CET
  • 5 pm CET


Meet the Presenters

Dr. Andreas Schwab
Global Head of Medical Software TCC, Senior Lead Auditor and Product Expert.
Dr. Christoph Ziskoven
Global Head and Program Manager of the Technical Competence Centers for Medical Devices.

Don’t miss out on this valuable session - register today!

Register now
You will receive a confirmation of your registration by e-mail. After the event, we will provide you with the presentation as a download. For questions and further information, we are also available in advance.

There are no participation fees for you by participating in the events. In return for attending our webinar, we only request your contact details and your consent to receive regular e-mail updates on TÜV Rheinland products and news in the future. The fields marked with * are required for a region-specific contact to coordinate conversations. This enables us to process your inquiries quickly and competently.


© TÜV Rheinland 2025
 
Back to top