UK Responsible Person, Swiss and EU Authorised Representative
If you are a Medical Device and/or an In-Vitro Diagnostic manufacturer, located outside of UK, Switzerland and the EU, and are selling to UK Switzerland and EU, you will need to appoint a UK Responsible Person, Swiss Authorised Representative and an EU Authorised Representative.
With offices based in Brighton - UK, Galway - Ireland, and Bülach - Switzerland, Psephos will take on the role of UKRP, CH-REP and EUAR, providing you with legal and easy access to all regions.
Why appoint Psephos to be your Responsible Person and/or Authorised Representative?
20+ years of experience and integrity working within UK Health infrastructure
Dedicated and supportive Representative Services Team
Independent consultancy with no conflict of interest
Quotations are bespoke with no unexpected or hidden fees
Insurance to cover liability
When you get in touch with us you will be asked to confirm the number of devices that you would like to register, and how many technical files that would involve. Once we receive this information, we will provide you with a tailored quotation and support you with any questions that you may have.