From “Essential Requirements” to “General Safety and Performance Requirements” – EU MDR 2017/745
December 27, 2018
Technical Documentation for medical devices under the new European MDR
December 20, 2018
Conformity Assessment Procedures and Premarket Scrutiny under EU MDR
December 3, 2018
Classification of medical devices under the European Medical Device Regulation 2017/745
November 12, 2018
Switzerland
- confinis ag, Hauptstrasse 16, CH-3186 Düdingen, Switzerland
- info.ch@confinis.com
- +41 26 494 8 494
- confinis corp., 4445 Willard Ave, Suite 600, Chevy Chase, MD 20815, USA
- info.usa@confinis.com
- +1 240 252 0891