Changes to the way medical devices adverse incidents are reported to the MHRA
The way incidents are reported and the systems that support this process are changing. If you are currently registered with the Manufacturer’s Online Reporting (MORE) portal, or send the XML output of the Manufacturer Incident Report (MIR) form to the MHRA’s mailbox; firstname.lastname@example.org, the MHRA would like to invite you to join their webinar to find out more about the changes to reporting coming later this year. The webinar is due to be held on the 11th August 2022 from 13:00 to 14:30 BST and again on 18th August 2022. If you wish to join the webinar, please click here to register.