The EU HTA Regulation: Webinar for health technology developers of high-risk medical devices and IVDs
Van derden19/06/26
In this webinar, Chairs and Co-chairs of the Member State Coordination Group on Health Technology Assessment (HTACG) and its subgroups will explain the process for joint clinical assessments (JCA) and joint scientific consultations (JSC) for high-risk medical devices and in vitro diagnostic medical devices (IVDs). The webinar will also cover relevant guidance documents adopted by the HTACG.
In addition, the HTA Secretariat of the European Commission will explain the relevant administrative and IT processes, including how to access and use the HTA IT Platform for the JSC and JCA workflows.
The webinar is targeted at representatives of health technology developers of high-risk medical devices and IVDs. Register here.