The European Commission launched, on Wednesday 28 May, an online public consultation on joint clinical assessments of medical devices and in vitro diagnostic medical devices at EU level under the Health Technology Assessment (HTA) Regulation. This online consultation is open to responses until 25 June 2025.
It focusses on the last implementing act for adoption under the HTA Regulation, which will complete the legislative framework for its implementation.
On Monday 2 June, the Commission also opened the second submission period for joint scientific consultations (JSCs) under the EU Health Technology Assessment Regulation.
JSCs enable health technology developers to consult on the planning of their health technology clinical studies. The period for submitting applications is open from 2 to 30 June 2025 to developers of both medicinal products and medical devices.
Link to the draft act: https://aeur.eu/f/h4m (Original version in French by Lionel Changeur)