If you're a non-UK manufacturer, appointing a UK Responsible Person (UKRP) is mandatory for placing medical devices on the UK market.
At Aurevia, we provide end-to-end UKRP support to simplify your compliance journey:
✔ Acting as your official UK point of contact
✔ Supporting MHRA registrations
✔ Reviewing technical documentation before submission
✔ Guiding you through evolving UK regulatory requirements
✔ Providing ongoing regulatory support
Our goal? To make UK market access straightforward, efficient, and compliant—so you can move forward with confidence.
Beyond our UKRP services, we offer quality and regulatory expertise to support compliance across your full product lifecycle—from regulatory strategy and QMS to audits and post-market activities.
Learn more about our quality and regulatory services and UKRP services.