The new MORE portal is available for submission of reports relating to adverse incidents for devices.
The legacy MORE portal is now read only. You will not be able to submit any reports via this route.
You must register with us for a new MORE account to be able to use the new MORE portal and/or API. Details of how to do this can be found on the
Historical reports from your old MORE account will not be available in your account after 30 April 2023. If required, you must download historical reports for your own record. Any draft reports in your old account will need to be re-created in your new MORE account for submission.
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.loginMORE
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