UK Responsible Person Services

If you are a medical device manufacturer based outside the UK, you must appoint a MHRA UK Responsible Person (UKRP) if you intend to place your devices on the UK market. The UKRP plays a vital role in ensuring that your devices comply with all relevant UK regulations and standards.


Do you need UKRP services?

Are you:

An IVD and/or MD manufacturer?

Based outside the UK?

Planning to sell your products in the UK?

If you answered “yes” to any of these questions, you will need the services of a UK Responsible Person.

Are you:

An IVD and/or MD manufacturer?

Located in the UK or outside the EU?

Sell your products in the EU?

If so, you will need an

Authorised Representative.

Responsibilities of a UKRP:

The UKRP has a number of responsibilities, including

  • Registering your devices with the Medicines and Healthcare products Regulatory Agency (MHRA)
  • Maintaining the technical documentation for your devices
  • Ensuring that your devices are manufactured in accordance with applicable regulations and standards
  • Investigating and reporting any adverse incidents involving your devices
  • Respond to MHRA requests for further information or documentation


How we can help:

We offer a comprehensive range of MHRA UK Responsible Person services to ensure your compliance with all applicable UK regulations and standards. Our services include

  • UKRP appointment
  • Device registration with the MHRA
  • Technical Documentation Review and Maintenance
  • Quality Management System review and implementation
  • Adverse event reporting and investigation
  • MHRA liaison

Our team consists of experienced and qualified UKRP professionals who can guide you through all aspects of UKRP compliance. We are proud members of the UK Responsible Person Association (UKRPA), a trade association for UKRP providers.


Additional benefits


  • We have a thorough understanding of the UK regulatory landscape and can keep you informed of the latest changes.
  • We offer a personalised service, tailoring a UKRP compliance plan to meet your specific needs.
  • We are committed to providing a high level of service and support.

Find out more about our UKRP services and how we can help you place your medical devices on the UK market.

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