In the medical device industry, the cybersecurity threat is ever increasing, and malware attacks are believed to endanger patient lives severely. Authorities have agreed to strengthen cybersecurity to counter this, however many standards are not yet harmonized and require some interpretation.
This on-demand webinar provides an insight into TÜV SÜD’s interpretation, as well Team NB’s, on cybersecurity requirements for MDR/IVDR. The expert will also provide more information on State-of-the-Art requirements that are essential to achieve and maintain market authorization.
Our on-demand webinar tackle these points, focusing on:
- Motivation
- Regulatory landscape
- Key messages from MDR & MDCG 2019-16
- Latest Cybersecurity standards
- Tips for Technical Documentation submission & audits
- Common pitfalls of Technical Documentation submissions
- Q&A (15 mins)
About the speaker
Speaker
Jan Küfner
Senior Product Specialist, TÜV SÜD
