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
Your insight to: confinis and its partners – work in progress regarding MDR implementation
September 4, 2018
MDR Article 117 – a look into the Crystal Ball (Part 6)
September 3, 2018
From Investigator to Consulting: On the other side of the fence
September 3, 2018
Switzerland
- confinis ag, Allee 1B, CH-6210 Sursee, Switzerland
- info.ch@confinis.com
- +41 26 494 8 494
- confinis corporation, 15807 Glacier Ct, North Potomac, MD 20878, USA
- info.usa@confinis.com
- +1 240 252 0891
Call us at +41 26 494 8 494 (CH) or +1 240 252 0891 (USA)
Mail us at info.ch@confinis.com (CH) or info.usa@confinis.com (USA)
Find us at Hauptstrasse 16 3186 Düdingen, Switzerland 15807 Glacier Ct North Potomac, MD 20878, USA