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UK MHRA · UK · 5 Sep 2025 · Guidance

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

From UK MHRA

This document is intended to guide manufacturers on what data to include within a Post market surveillance report (PMSR). It is not mandatory to include sections which do not apply, and data may be displayed in an alternative form if appropriate.

Excerpt from the official page. The original is authoritative.