The EU HTA Regulation: Webinar for health technology developers of medical devices and in vitro diagnostic medical devices

Van derden

12/12/25

In this webinar, Chairs and Co-chairs of the Member State Coordination Group on Health Technology Assessment and its subgroups will explain the process for joint clinical assessments and joint scientific consultations for high-risk medical devices and in vitro diagnostic medical devices.

In the second part of the webinar, the European Commission will demonstrate the HTA IT Platform which is used for secure exchange of information with health technology developers.

The webinar is targeted at representatives of health technology developers of high-risk medical devices and in vitro diagnostic medical devices.

Practical information