Peter 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, 2018Classification of medical devices under the European Medical Device Regulation 2017/745
November 12, 2018#MDR – Transition periods and definitions
October 22, 2018Work in progress: MDR implementation – impact on your Quality Management System (ISO 13485:2016)
September 22, 2018Your insight to: confinis and its partners – work in progress regarding MDR implementation
September 4, 2018MDR Article 117 – a look into the Crystal Ball (Part 6)
September 3, 2018