Join us for a webinar dedicated to the evolving regulatory and compliance landscape for medical devices in the EU and Belgium.

From the latest developments in the MDR/IVDR revision to the practical challenges of keeping regulatory and clinical teams aligned throughout the device lifecycle, this conference brings together legal and regulatory experts to address the issues that matter most to industry professionals today.

The programme opens with a timely update on the MDR/IVDR revision, followed by an in-depth look at how regulatory and clinical functions can stay aligned across the medical device lifecycle to avoid costly missteps. After a short break, the focus shifts to medical device advertising, with a practical review of EU and Belgian rules illustrated through real-world examples.

Whether you work in regulatory affairs, compliance, clinical operations, or marketing within the medtech sector, this conference offers practical insights and direct access to experienced practitioners who navigate these issues on a daily basis