United Kingdom Responsible Person Services

The regulations for marketing authorization of medical devices in the UK changed in January 2021 after the UK left the European Union. The previous CE mark will no longer valid in the UK, and will be replaced by the UKCA mark. The CE mark will continue to be valid during a limited transition period. All non-UK manufacturers are now required by law to appoint a UK Responsible Person (UKRP) to enable them to register their products on the British market with MHRA.

Available to foreign medical device manufacturers wishing to sell their products in the United Kingdom


Contact us for an information pack and application form with the product registration details. 
  • Fast and reliable consulting services
  • Experienced medical device specialists with global expertise
  • Cost-effective plans with 2-5 year service contracts
  • Full guidance and support provided
  • Regular communication and reports provided to clients
  • The fully managed process from registration to field complaint handling
  • Thorough document examination and advice
  • Transparent processes throughout our relationship
  • Free advice on regulatory issues as required
  • Updates provided on new regulations and standards as they change
  • We will work with your distributors to ensure they are in compliance
  • Business development services also available


MCT Lifesciences has over 30 years of experience in the international medical device industry.

Quality is not an accident, it's a culture

MCT-Lifesciences Services

We specialise in helping companies to find new markets for their products across Europe, the Middle East and North Africa. Expanding outside your home country can be daunting and feel overwhelming, however our team has over 30 years experience in making international expansion a success.

Our core service offering

Considering expansion?

If you are considering expanding your sales in a new country, contact us today for more information and professional advice.