Cybersecurity for Medical Devices: Regulatory Challenges and Key Considerations

How can we balance technological innovation, device performance, and safety throughout the entire lifecycle?
In this webinar, we will cover: 

• An analysis of the key cybersecurity requirements applicable to medical devices, based on major references (European regulations, FDA recommendations, IEC 60601-4-5 and IEC 81001-5-1 standards, etc.).
• A closer look at the process of a medical device safety audit
• A Q&A session

Participation is free, but registration is required.

Date:
June 2, 2026, from 11:00 a.m. to 12:00 p.m.