Statut et Classification des dispositifs borderlines selon le règlement (UE) 2017/745
Guidance on Qualification and Classification of Software in Regulation (EU) 2017/745 – MDR and Regulation (EU)
Nouveaux règlements européens pour les dispositifs médicaux - ANSM : Agence nationale de sécurité du médicament et des produits de santé
Conformité à l'IVDR : 10 conseils pour les fabricants de dispositifs médicaux
Italy: Bills to implement Regulation (EU) 2017/745 and Regulation (EU) 2017/ 746 on medical devices and in vitro diagnostic medical devices - Global Compliance News
PE-CONS 79/1/21 REV 1
Évaluation, désignation et notification des organismes d'évaluation de la conformité en France - ANSM
Regulation (EU) 2017/746 for Medical Device
In vitro diagnostic software: Novelties introduced by Regulation (EU) 2017/ 746 - GMED Medical Device Certification
Introduction to the Regulation (EU) 2017/746 - GMED Medical Device Certification
EU IVDR 2017/746 | BIOMEDRIC
In Vitro Diagnostic Regulation (IVDR) (EU) 2017/746 - omcmedical.com
Europe - Manual on borderline and classification for medical devices under Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (Revised) - RIS.WORLD
Downloads | MDRC
Table ronde sur l'IVDR au Forum DMDIV - SIDIV
Questions & Answers on Implementation of the Medical Devices and In Vitro Diagnostic Medical Devices Regulations ((EU) 2017/
Dispositifs médicaux de diagnostic in vitro (dmdiv)
DeviceMed.fr - DeviceMed.fr
IVD: implementation and preparedness plan for IVDR. How to prepare?
IVDR 2017/746 Compliance Definition | Arena
IDS049 - Élaboration de la Documentation Technique selon le Règlement 2017/ 746 - Mise à jour et amélioration du Système de Management de la Qualité selon ISO 13485 : 2016 - Bibliothèque des travaux Master
Transition to EU IVD Regulation (EU) 2017/746 and considerations for non-EU regulatory authorities on managing the impact to pro
IVD Directive to IVD Regulation (EU 2017/746) Transition – 8 Months Remaining - Voisin Consulting Life Sciences
A Summary of (EU) 2017/745 and (EU) 2017/746 - A Must Read for Medical Device Manufactures
