UK MHRA mandates Medical Device manufacturers located outside the United Kingdom (UK) and without any local business offices for MHRA UK Responsible Person registration. Manufactureres need to appoint a United Kingdom Responsible Person (UKRP) or UK Representative on their behalf, as a pre-requisite for device registration and launch of the device in the United Kingdom.


https://www.ukrpservices.com/a....-step-by-step-guide-

UK Responsible Person Toolkit
Avail a complete set of guidance documents, templates and exhaustive checklists to ensure successful device registration

https://www.ukrpservices.com/

 

www.ukrpservices.com

UK Responsible Person Services for Medical Device Manufacturers

Freyr provides UK Responsible Person (UKRP) services to foreign medical device manufacturers for product registration and market entry in the UK.