UK Government Discover Pro-Innovation Regulatory Reforms for Faster Medical Device Approvals
Great Britain, 22 October 2025 – UK Government’s plan to simplify and modernize regulatory frameworks to enable faster market access for innovative technologies across healthcare, life sciences, and other sectors. Key actors involved include the Medicines and Healthcare products Regulatory Agency (MHRA), Department for Science, Innovation and Technology, and the Regulatory Innovation Office (RIO). Looking […]
Europe quietly arms itself for device-level HTA and what it means for the U.S., Canada, Asia & Africa
Europe, 22-10-2025 — Global Health Technology Assessment: The European Commission’s Health & Food Safety directorate published a newsletter on 17 October announcing that it has adopted the procedural rules for Joint Clinical Assessments (JCAs) of medical devices and IVDs under the EU Health Technology Assessment Regulation (HTAR). The item also points to the Commission’s hub […]