Theme Re-assessment of notified bodies Target Audience Designating authority, NB Products concerned MD Documents mentioned MDR (EU) 2017/745 article 46 MDCG 2022-13 This document provides a template form for use by designating Authorities (NAs) in the reassessment...
Publications : Borderline
MDCG 2024-5 – Guidance on content of the Investigator’s Brochure for clinical investigations of medical devices – April 2024
Theme Investigator’s brochure Target Audience Sponsor of clinical investigations Products concerned MD Documents mentioned MDR (EU) 2017/745 : – article 70 – Annex XV Chapter II Section 2 ISO14155:2020 This guidance document is intended to assist sponsors of...
MDCG 2024-4 – Safety reporting in performance studies of in vitro diagnostic medical devices under Regulation (EU) 2017/746 – Avril 2024
Theme Safety reporting in performance studies Target Audience Sponsor of performance studies Products concerned IVD Documents mentioned IVDR (EU) 2017/746 : article 76 In a context where the Eudamed electronic system for performance studies is not available, this...
Delphine Dominé
I’m a pharmacist specialized in Regulatory Affairs. During my university studies, I had the opportunity to acquire a lot of knowledge and skills, which reinforced my choice of a career in regulatory affairs in the healthcare field. I joined nexialist in 2024 as a...
MDCG 2024-3 – Guidance on content of the Clinical Investigation Plan for clinical investigations of medical devices – March 2024
Theme Clinical investigation plan (CIP) Target Audience Sponsor of clinical investigation Products concerned MD Documents mentioned RDM (EU) 2017/745 - article 70 - annex XV ISO14155:2020 This guide is intended to help sponsors draw up their clinical...
MDCG 2024-2 : Procedures for the updates of the European Medical Device Nomenclature
Theme European Medical Device Nomenclature (EMDN) Target Audience All the actors Products concerned MD, IVD Documents mentioned RDM (UE) 2017/745 – article 26 RDIV (UE) 2017/746 – article 23 This guide relates to the : revision of the European Medical Device...
MDCG 2024-1 Guidance on the vigilance system for CE-marked devices – DSVG 00 Device Specific Vigilance Guidance Template
Theme Vigilance Target Audience Manufacturers Products concerned Specific devices : cardiac ablation, coronary stents, cardiac implantable electronic devices, breast implants Documents mentioned MDR (EU) 2017/745 – articles 87 et 88, 92 IVDR (EU) 2017/746 –...
MDCG 2023-7 Guidance on exemptions from the requirement to perform clinical investigations pursuant to Article 61(4)-(6) MDR and on ‘sufficient levels of access’ to data needed to justify claims of equivalence
Theme Clinical investigation exemption, demonstrating equivalence Target Audience Manufacturers Products concerned Class III and implantable MD Documents mentioned MDR (EU) 2017/745 – Article 61(4)-(6) MDCG 2020-5 MDCG 2020-6 MDCG 2020-8 This MDCG guide aims...
MDCG 2023-6 – Guidance on demonstration of equivalence for Annex XVI products – A guide for manufacturers and notified bodies
Theme Clinical evaluation, demonstrating equivalence Target Audience Manufacturers, notified bodies Products concerned Products without an intended purpose listed in Annex XVI of MDR Documents mentioned MDR (EU) 2017/745 - Annex XIV, Annex XVI Implementing...
Souha Dachraoui
I worked as a physiotherapist for two years, after that I worked as a medical representative for a pharmaceutical laboratory. Then I decided to broad my skills and get a degree in Engineering and Ergonomics of Physical Activity before completing my academic career...