UK MHRA · March 30, 2026

Guidance: Clinical investigations: investigators' responsibilities

MHRA guidance on investigator responsibilities for conducting clinical investigations on medical devices to meet regulatory requirements.

Medium impact Medical Devices UK medical-devicesclinical-evaluationpost-market-surveillance

How to make sure your clinical investigation will meet the MHRA's requirements for medical devices.

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