Any manufacturer incorporated outside the United Kingdom who places medical devices or IVDs on the Great Britain market must appoint a UK Responsible Person. This is a requirement under the UK Medical Devices Regulations 2002 (as amended) and is not optional.
The UKRP is registered with the MHRA, named in device registration records, and carries defined obligations — including managing vigilance reports, field safety corrective actions, and post-market surveillance correspondence.
Cyberpan Support Services Ltd holds an active UKRP registration. We act as your UKRP for the duration of the appointment, handling all MHRA-facing obligations on your behalf. Fixed annual fee. Defined scope.