BNS webinar on CTIS and medical device regulations

On 15 December 2025, we welcomed Audrey Van Scharen, Master in Laws and Vice-President of the Ethics Committee at Vrije Universiteit Brussel (VUB), for an insightful webinar on the evolving European regulatory landscape.

During this session, Audrey provided a clear overview of the new CTIS regulations and their impact on the conduct of clinical trials across Europe. She also explored recent and upcoming developments in medical device regulations, highlighting key implications for researchers, sponsors, and regulatory professionals.

The webinar offered valuable guidance for anyone involved in European clinical research or medical device development who needs to stay compliant with the latest regulatory frameworks.

Missed the session or want to revisit the key points? You can now access the presentation slides from the webinar here.