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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
How to use a quasi-experimental study to evaluate your digital health product.
Find out about the Industry Security Assurance Centre (ISAC) and its associated responsibilities.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidance relating to blood clotting, myocarditis and Guillain-Barré Syndrome (GBS) after COVID-19 vaccination.
Find out if your ivory item may qualify for the pre-1918 outstandingly high artistic, cultural or historical value exemption, how to apply and what to do if it is refused or revoked.
A guide for organisations interested in being an 'attribute service provider' certified against the UK digital identity and attributes trust framework.
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