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MHRA (UK)
Original article

Guidance: Clinical investigations: compiling a submission

RegulatoryNeutral
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Summary

MHRA has issued guidance on how to notify the agency for undertaking clinical investigations of medical devices, providing procedural requirements for compiling submissions.

Importance:2/10
Sentiment:
0.00
medical deviceclinical investigationregulatory guidanceMHRA
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Published by MHRA (UK) on August 6, 2026 7:16 AM

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