UK MHRA · March 31, 2026

Guidance: Clinical investigations: compiling a submission

Guidance on how to notify the MHRA of a planned clinical investigation of a medical device.

High obligation Sector Medical Devices & IVD Clinical Trials & Research UK Medical devicesClinical evaluation

How to notify the MHRA that you are going to undertake a clinical investigation of a medical device.

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