You need a new European Authorised Representative (EAR)
in accordance with the the EU Regulations 2017/745 & 746

  • Medical Devices (MDR)

  • In Vitro Diagnostics (IVDR)

You have to think about

Your devices on the European Market

Discover our services as an EAR

A Team of
Senior Experts

Our team is composed of Senior Experts in the field of regulation of medical devices

Your Representative for
EU Regulations

TNA & Partners can represent you in the European Union according to the Regulation in force

Quality and Security for Your Development

Our expertise and our agility is the guarantee of a high level of quality and security for your development in the EU

4 reasons to choose TNA & Partners


Our Chairman is a PharmD, expert in MD/IVD


All partners have a long experience in EU Regulation​


We maintain a Quality System for our organisation​


Each member of our team is a qualified Person Responsible for Regulatory Compliance (PRRC)​