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

You may need to carry out a clinical investigation as part of the process to obtain a CE marking for your medical device. You must inform MHRA if you are planning to do this at least 60 days before starting your investigation. The MHRA have updated their guidance on this process to include information about new requirement to pay fees for amendments published.

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Published on 3. April 2017 in News UK