Medical devices: post-market surveillance Page summary: Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA. Change made: Updated to provide the latest information regarding the MORE portal. Time updated: 12:08pm, 16 May 2025 Manufacturer’s Online Reporting Environment (MORE) Page summary: A a digital platform designed to facilitate the reporting,…
Ben KempMay 23, 2025