UK Responsible Person appointment
Formal UKRP representation for manufacturers established outside the United Kingdom, with clear responsibilities and direct regulatory contact.
UK Responsible Person
A trusted regulatory presence in Great Britain.
UKRP representation for overseas medical device and IVD manufacturers—providing more than an address on the label.
Personal representation backed by regulatory expertise.
RHQC combines the formal UK Responsible Person function with practical consultancy capability. Overseas manufacturers receive direct access to experienced leadership rather than a purely administrative registration service.
Support covers initial review and appointment, MHRA registration, ongoing maintenance, vigilance and the wider UK market-entry requirements affecting the device and supply chain.
MHRA registration
Initial device registration, manufacturer and device data management, change notifications and ongoing maintenance of UK market records.
Documentation verification
Verification that declarations of conformity, conformity-assessment evidence and required technical documentation are available and appropriately maintained.
Labelling & market-entry review
Review of UKRP details, UKCA or recognised CE pathways, importer and distributor obligations, labelling and supply-chain readiness.
Vigilance & authority liaison
Support with reportable incidents, field safety corrective actions, MHRA communication and access to required records.
Ongoing UK compliance
Monitoring relevant regulatory change, maintaining registration information and providing responsive support throughout the commercial relationship.
Start a conversation