UK Responsible Person (UKRP)

A legal requirement for medical device and IVD manufacturers based outside the UK who place products on the Great Britain market.

What are UK Responsible Person services

Fixed Annual Fee
Cyberpan Support Services Ltd

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.

What we do

Who needs this?

What you'll receive

Named UKRP registration with the MHRA, structured reporting schedule, and access to regulatory liaison support throughout the engagement period. All correspondence managed and documented.