Medical devices: post-market surveillance

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: Added link to guidance for ‘Medical Devices: Standardised format for post market surveillance report (PMSR)’ Time updated: 3:14pm, 5 September 2025

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: Link added for ‘Documentation for implementation of data requirements under the new Post-Marketing Surveillance regulations’ Time updated: 12:00pm, 9 June 2025