UKRP – UK Responsible Person

In order to legally sell medical devices in the UK, a manufacturer must designate a UKRP. The UKRP has been appointed by the Overseas Manufacturer to act as their representative in the UK. The UKRP will then be responsible for ensuring that the product complies with all applicable requirements.

We provide UKRP Services to assist companies who wish to register their products as Medical Devices in the UK.

The UKRP service provides advice and guidance on how to comply with the requirements of the MDR Directive. It also covers the obligations of the company to ensure compliance with the MDR Regulation and any relevant national legislation.

Contact us today to find out more about our services.

UKRP – UK Responsible Person