Freyr Solutions simplifies the entire UK MHRA medical-device registration process by verifying the manufacturers technical documentation and managing submissions on MHRA's Device Online Registration Portal . As a designated UK Responsible Person (UKRP), we liaise directly with the MHRA for device registrations, vigilance activities ensuring full MHRA post-market compliance. Our experts help you introduce your CE marked devices in UK, transition from CE to UKCA marking, manage and support vigilance activities, and keep you informed of the regulatory updates on a periodic basis so you can focus on market growth while ensuring compliance to the regulatory requirements in the UK.