A UKRP Services for Foreign Manufacturers is a legal entity or individual based in the United Kingdom who acts on behalf of a foreign manufacturer of medical devices or in-vitro diagnostic (IVD) devices. Since Brexit, any non-UK manufacturers wishing to place their products on the UK market must appoint a UKRP to ensure compliance with UK medical device regulations.Following the UK’s departure from the EU, foreign medical device manufacturers can no longer rely on their European Authorised Representative to access the UK market. The UKRP is now a mandatory requirement for registering devices with the MHRA and managing regulatory compliance within Great Britain.