UK Responsible Person (UKRP) services
Supporting your access to the UK medical device market.
UK Responsible Person (UKRP)
Aurevia provides UK Responsible Person (UKRP) services to help non-UK manufacturers meet UK regulatory requirements and successfully place their medical devices and IVDs on the UK market. As a founding member of the UK Responsible Person Association (UKRPA), our UK-based company QAdvis UK Ltd. is part of a strong professional network, enabling us to provide efficient and reliable support for access to the UK market.
Supporting UK market access
For medical device manufacturers based outside the UK, appointing a UKRP is a legal requirement for placing medical devices on the UK market. The UKRP ensures your compliance with UK regulations and acts as your representative towards the Medicines & Healthcare Products Regulatory Agency (MHRA).
UKRP services
We provide UKRP services designed to provide full regulatory coverage, including:
- Acting as your official UK Responsible Person
- Review of technical documentation prior to UK registration
- Device registration with MHRA
- Inclusion of importers as part of the registration process
- Ongoing regulatory support and guidance
We ensure your documentation is accurate, complete, and aligned with UK requirements before submission.
Why choose us?
- UK-based legal entity (QAdvis UK Ltd.) providing UKRP services
- Founding member of the UK Responsible Person Association (UKRPA)
- Strong regulatory expertise and proven industry experience
- Dedicated team ensuring long-term compliance and support
From initial setup to ongoing compliance, we simplify regulatory operations by helping you navigate complexity and reduce administrative burden.
Leena Raunio, Quality & Regulatory Affairs Manager
Meet one of our UKRP experts
Our UK Responsible Person (UKRP) services are delivered by a team of regulatory specialists with in-depth expertise in UK requirements. We support non-UK manufacturers in placing medical devices and IVDs on the UK market, ensuring compliance and acting as your official point of contact with the MHRA.
With a strong understanding of the UK regulatory landscape, our experienced team provides reliable and responsive support across the entire product lifecycle.
To reach out to the UKRP team, submit the form below or email us directly at ukrp@aurevia.com.
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