UK Responsible Person, Swiss and EU Authorised Representative

All options must apply to you:

  1. A MD and/or IVD manufacturer?

  2. Located outside UK, Switzerland and EU?

  3. Selling to the UK, Switzerland and EU?

UK Responsible Person, Swiss &

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.

For more information on each of these roles, please refer to the UK Responsible Person page, the Swiss Authorised Representative page and to the EU Authorised Representative page.

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

ce.gif
UKCA black fill.png

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.