Development of medical devices to tackle COVID-19 – UPDATE
May 7, 2020
Swiss Medtech Umfrage: Export in die EU mit Drittstaatanforderungen sichern
May 1, 2020
Peter Studer joins confinis as Senior Advisor
April 27, 2020
EU MDR audit requirements and links to MDSAP program
February 14, 2019
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
#MDR – Transition periods and definitions
October 22, 2018
Work in progress: MDR implementation – impact on your Quality Management System (ISO 13485:2016)
September 22, 2018
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