Updated Guidance on Notifying the MHRA about a Clinical Investigation for a Medical Device

As part of the CE marking process you may need to carry out a clinical investigation for your medical device. You must inform MHRA if you are planning to do this at least 60 days before starting your investigation.

To view the updated guidance for manufactures on legislation for clinical investigations of medical devices, please click here.

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Published on 10. March 2016 in News UK