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
Competences
Our Chairman is a PharmD, expert in MD/IVD
Experience
All partners have a long experience in EU Regulation
Quality
We maintain a Quality System for our organisation
Reliability
Each member of our team is a qualified Person Responsible for Regulatory Compliance (PRRC)