New Industry UKARA Association Launched to Ensure UK Authorised Representative and Responsible Person Standards Expected by the UK Government

The UK Competent Authority for medical devices, the MHRA, requires manufacturers not domiciled in the UK must appoint a formal UK Responsible Person (UKRP) or UK Authorised Representative (UKAR) to be able to continue placing medical devices on the UK market. Following several months’ consultation with UK stakeholders, the newly-launched United Kingdom Authorised Representative Association (UKARA) was created to [PR.com]