"Freyr provides United Kingdom Responsible Person (UKRP) services to foreign medical device manufacturers in product registration and market entry in the UK and acts as a single point of contact in the Country for liaison with Regulatory Agency.
Freyr UKRP Services include –
Representing your device in the UK
Liaising with UK MHRA on your behalf
Registration of your devices with UK MHRA
30 minutes of pre-purchase free consultation
Review of technical file for UK MHRA compliance
Freyr name on label"