From 1st Jan 2020, MORE will be updated to reflect the latest version of the Manufacturer’s Incident Report (MIR) form. Further guidance is available on the EC website under Guidance MEDDEVs 2.12 Post-Market Surveillance.
Welcome to MORE – the Manufacturer's On-line Reporting Environment. This system has been especially designed by the MHRA to provide device manufacturers and suppliers and their authorised representatives, a simple electronic means of submitting Vigilance reports to the Agency and of providing responses to MHRA incident investigations.
Registered Users - Registered Users may log in below.
Not yet registered? - If you have not yet registered as a MORE account holder, click the link above and submit the requested details for verification. Please note that the provision of certain information is compulsory for registration. On-line Help is available if required.
For security reasons, new accounts will not be activated until registration details have been checked and verified by the MHRA.
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In the wrong place? - If you are not a manufacturer but are a medical device user - whether a healthcare or social care professional, or a patient or member of the public - there are separate reporting arrangements for you. Click here to return to our other online report forms