UK Responsible Person (UKRP) Requirements & Compliance Guide

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Since Brexit, appointing a UK Responsible Person (UKRP) has become a core requirement for most non-UK medical device manufacturers entering the Great Britain market. The role looks familiar (it resembles the EU Authorised Representative), but its obligations under the UK MDR 2002 (as amended) are distinct, legally binding, and far more visible to the MHRA.

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