Some important features regarding Europe’s Eudamed database

Conformity with Eudamed database under the European Medical Devices
Regulation (MDR) and in-vitro Diagnostics Regulation (IVDR) may be some time
away but organisation for the new requirements will take continuous work.

contact us for further information

Posted on 10. Oktober 2018
↑ back to top
picture kazurabashi vine bridge

Many bad traps are hidden
in the EU regulatory jungle
We guide you safely

mdi Europa facebook profile mdi Europa linkedin profile

News in Brief


grafik CE mark