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, monitoring, and management of medical device incidents.
Change made:
First published.
Time updated:
12:08pm, 16 May 2025
MORE implementation
Page summary:
Guidance on the updates to reporting forms following implementation of the Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024.
Change made:
First published.
Time updated:
12:08pm, 16 May 2025
