Keeping registration up to date
How manufacturers and UKRPs must maintain their MHRA registration throughout the device lifecycle — when to update registrations, what changes trigger an update obligation, and the consequences of outdated registration.
Notifying changes to MHRA
Which changes to a device, its manufacturer, or its UKRP must be formally notified to MHRA — and which changes are handled through registration update vs. separate notification.
Annual fees
MHRA annual registration and compliance fees for medical device manufacturers and UKRPs — fee structure, payment, and what happens if fees are not paid.