Swiss Medtech Umfrage: Export in die EU mit Drittstaatanforderungen sichern

Peter Studer joins confinis as Senior Advisor

EU MDR audit requirements and links to MDSAP program

From “Essential Requirements” to “General Safety and Performance Requirements” – EU MDR 2017/745

Technical Documentation for medical devices under the new European MDR

Conformity Assessment Procedures and Premarket Scrutiny under EU MDR

Classification of medical devices under the European Medical Device Regulation 2017/745

#MDR – Transition periods and definitions

Work in progress: MDR implementation – impact on your Quality Management System (ISO 13485:2016)

Your insight to: confinis and its partners – work in progress regarding MDR implementation

MDR Article 117 – a look into the Crystal Ball (Part 6)

From Investigator to Consulting: On the other side of the fence

MDR Article 117 – a look into the Crystal Ball (Part 5)

WORKSHOP: PMS under the new European MDR

“Quick Wins” for your MDR implementation

MDR Article 117 – a look into the Crystal Ball (Part 4)

MDR Article 117 – a look into the Crystal Ball (Part 3)

MDR Article 117 – a look into the Crystal Ball (Part 2)

MDR Article 117 – a look into the Crystal Ball (Part 1)

confinis opens US office in the Washington DC area

New year, new energy!

Beat Steffen to speak at Medtech & Pharma Platform in Basel