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How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
RA1, RA2, RA3, RA4, RA5 bilingual forms for completion following a drugs test in custody.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Information about the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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