Sites
Approved contributions by @freyrsolutions to the Viesearch index.
MHRA UK Responsible Person Registration Overview
UK MHRA mandates Medical Device manufacturers outside of the UK to register with a UK Responsible Person (UKRP) for device registration and launch.
Medical Device Regulatory Consulting
Freyr provides end-to-end Medical Device Regulatory services, compiling device documentation, and acting as an in-country representative.