UK MHRA updates how to report medical device vigilance 14 Dec 2022

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has updated the way to report adverse incidents involving medical devices.

Now manufacturers can submit incidents via the new MORE portal.  A new registration is required.

The previous MORE portal can no longer accept reports, although existing reports can be downloaded until 30 April 2023.

Further information and registration available via the link.