EPF's feedback on joint scientific consultations on medical devices

This month, EPF provided feedback on the European Commission's public consultation on joint scientific consultations on medical devices, under the upcoming EU Health Technology Assessment (HTA) Regulation.

In January 2025, the EU HTA Regulation will be implemented, providing a framework for EU HTA bodies to work together on the clinical aspects of health technology assessment. 

This month, EPF provided feedback on the European Commission's public consultation on joint scientific consultations on medical devices and in vitro diagnostic medical devices.

EPF calls for clear guidelines, diverse representation and support for patient involvement in joint work on medical devices and in vitro diagnostics. Patient organisations bring an essential, collective voice to HTA, ensuring that the process reflects the diverse experiences and needs of the community. Patient organisations should be actively involved in the identification and preparation of patient representatives, ensuring EU-wide diversity and transparency.

Read EPF's feedback here.