confinis celebrates 15th anniversary
June 2, 2020Webbased tool to analyze effect of significant changes to devices covered by MDD or AIMDD certificates
May 13, 2020Politics intervene regarding medical devices
May 8, 2020Development of medical devices to tackle COVID-19 – UPDATE
May 7, 2020Swiss Medtech Umfrage: Export in die EU mit Drittstaatanforderungen sichern
May 1, 2020Peter Studer joins confinis as Senior Advisor
April 27, 2020EU MDR audit requirements and links to MDSAP program
February 14, 2019From “Essential Requirements” to “General Safety and Performance Requirements” – EU MDR 2017/745
December 27, 2018Technical Documentation for medical devices under the new European MDR
December 20, 2018Conformity Assessment Procedures and Premarket Scrutiny under EU MDR
December 3, 2018