[2025-09-26] (Open access) Your 2025 training plan is not yet complete? Good news: you can still take action right now! Discover our INTER-enterprise training calendar for September, October and November, or ask us about our INTRA-enterprise on-site training sessions. We also offer e-learning courses on MDR and IVDR, with continuous
[2025-09-23] (Open access) Delegated Regulation (EU) 2025/1920 on the unique identification of optical medical devices (spectacle frames, spectacle lenses and ready-to-wear reading spectacles) was published in the Official Journal of the European Union on September 23, 2025. It follows the public consultation we reported on earlier this year. We invite
[2025-09-08] (Open access) The European Commission launched a call for evidence on September 8, 2025, to prepare a targeted revision of European regulations on medical devices (MD) and in vitro diagnostic medical devices (IVDD). The call for evidence is available in all European Union (EU) languages. You will need to
[2025-09-05] (Open access) Do you have a place at one of the upcoming EUDAMED workshops organized by the European Commission? The workshops, like the previous one held in Stuttgart on May 21, 2025, are free of charge, and always in a hybrid format: face-to-face and by videoconference. They will take
[2025-07-25] (Open Access) The European Commission continues to publish the results of its survey of Notified Bodies (NBs) with regard to the availability of medical devices (MDs) and in vitro diagnostic medical devices (IVDDs), on the European Union (EU) market. This is the 14th update. Survey background The survey was
[2025-09-19] (Open access) Team-NB (The European Association of Medical devices Notified Bodies) announces its 1st EU Regulations Discussion Day 2025. This event is aimed at small and medium-sized enterprises (SMEs), members of notified bodies and organizations. It aims to encourage exchanges between stakeholders on the future European regulatory framework for
