UK MHRA · September 05, 2025

Guidance: Medical devices: Standardised format for the post market surveillance report

MHRA provides standardised format and recommendations for manufacturers preparing post-market surveillance reports.

High obligation Framework Medical Devices & IVD UK Post-market surveillanceMedical devices

Information and recommendations for manufacturers on the preparation and presentation of a post market surveillance report (PMSR).

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Published by UK MHRA. HealthSignal links to the original document; the summary above is extracted from the source text.