➡️ From January 1st 2022, all devices sold in Great Britain and/or Northern Ireland are to be registered with the MHRA.
☑️ This registration shall be performed by the UK manufacturer or the UK Responsible Person (UK RP) of a non-UK manufacturer
☑️ UK Responsible Person acts as the main contact point to the MHRA and patient/users of the devices for non-UK manufactures. Amongst other responsibilities, the UKRP shall remain available to MHRA, keeping available all technical documentation that may be required for inspection.
☑️ If you do not have a UK RP appointed yet, ASPHALION can do it for you.
☑️ In case you would like to know more about this service, you can schedule a free 30 minutes consultation meeting at the Medical Devices calendar here:
https://outlook.office365.com/owa/calendar/[email protected]/bookings/
➡️ You can also contact us at: [email protected]
We will be more than happy to help you!
