When you need
to be sure

SGS Fimko Oy in Finland has officially been designated as a Notified Body under the European Union (EU) Regulation (EU) 2017/746 – In Vitro Diagnostic Medical Devices Regulation (IVDR).

Our comprehensive range of services helps organizations comply with many international, national, regulatory, and industry standards, and demonstrate their best practices.

Dual-use product testing must consider both military standards and civilian standards. SGS Fimko’s experts are familiar with both standards and know how to combine them effectively in testing processes.

In this publication, we list the latest changes and updates that affect the approval of products in international markets.