UK Responsible Person

The legal entity designated by a foreign manufacturer to act on its behalf in the United Kingdom.

Overseas manufacturers must appoint a UK Responsible Person (UKRP) to place medical devices on the market in Great Britain. The UKRP liaises with the MHRA, registers products in PARD, and ensures technical files are available for inspection.

Explore the data behind the terms

HaRi brings the FDA, MHRA, EUDAMED, Health Canada and TGA registers into one search: devices, manufacturers, product codes and safety events, all cross-referenced and free to explore.