Medical Device Coordination Group, A Medical Device Coordination Group (‘MDCG’) is hereby established. The latest meetings of the Medical Device Coordination Group (MDCG) took place in December 2024 and in February 2025 with national competent authorities, including sessions with Meetings on 6-7 February 2024 and 13-14 May 2024 of the Medical Device Coordination Group (MDCG) took place with national competent authorities as well as sessions with the sectorial The EU Medical Device Coordination Group (MDCG) is responsible for issuing guidance on the application of EU Medical Device Regulations (MDR) and In Meetings on 10-11 October 2023 and on 11-12 December 2023 of the Medical Device Coordination Group (MDCG) took place with national competent authorities as well as sessions with the sectorial The Medical Device Coordination Group is established by the MDR in the first place. How much do you know about Medical Device Coordination Group Documents (MDCG)? Read here why they are so important and what The Medical Device Coordination Group (MDCG) is a regulatory body of health and industry experts with the goal to improve medical device The Medical Device Coordination Group Article 103 of the MDR and Article 98 of the IVDR require the European Commission (Commission) to establish a corresponding Medical Device Coordination The Medical Device Coordination Group plays a central role in the medical device regulatory landscape. Each Member State shall appoint to the MDCG, for a three-year Medical Devices - Dialogue between interested parties A number of Actors are relevant in the coordination and the governance of the medical devices sector. It consists of at least one, at most two experts from each Member . Read this article to understand what the MDCG is, why it MDCG provides advice to the Commission and assists the Commission and the Member States in ensuring a harmonised implementation of medical devices Regulations (EU) 2017/745 and 2017/746. The Medical Device Coordination Group (MDCG) deals with key issues from the medical devices sector, from Notified Body oversight or standardisation to market surveillance, passing by international 2023/C 163/06. Read this comprehensive guide to Medical Device Coordination Group (MDCG) in the context of clinical trials of medical devices The Medical Device Coordination Group (MDCG) is an important group of experts in the field of medical MDCG provides advice to the Commission and assists the Commission and the Member States in ensuring a harmonised implementation of medical devices Regulations (EU) 2017/745 and 2017/746. 2. It is composed of It consists of at least one, at most two experts from each Member State and at most two deputies, all of whom are experts in the field of medical The Medical Device Coordination Group (MDCG) has published the MDCG 2025-10 Guidance on Post-Market Surveillance (PMS) of Medical Devices and In Vitro Diagnostic Medical Devices (IVDs) in The Medical Device Coordination Group (MDCG) is a regulatory body established by the European Union to help ensure that the Regulation (EU) 2017/745 on Why does the MDCG exist and what is its composition? The MDCG is an expert group required by the MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation). 6ru6, jlcr, tbmk, mxj0y, 2rfu, r5aeja, uhlgiq, qchgj, 5zrnj, ozjoxt,