MDCG 2020-16 rev.5 - Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746
Revised guidance on IVDR classification rules for in vitro diagnostic devices published.
EC Public Health · EU-wideRevised guidance on IVDR classification rules for in vitro diagnostic devices published.
EC Public Health · EU-wideAn Implementing Regulation establishes uniform requirements for conformity assessment and notified bodies under the medical device framework.
EC Public Health · EU-wideImplementing Regulation (EU) 2026/977 establishes uniform requirements for conformity assessment and notified bodies under the MDR/IVDR regime.
EC Public Health · EU-wideVersion 5 of the EC manual on borderline and classification decisions under MDR and IVDR published.
EC Public Health · EU-wideUpdated guidance on medical device classification issued by the Medical Device Coordination Group.
EC Public Health · EU-wideMDCG guidance on post-market surveillance obligations for medical devices and IVDs under MDR and IVDR.
EC Public Health · EU-wideMDCG guidance on practical application of UDI assignment responsibilities under MDR and IVDR.
EC Public Health · EU-wideCommission adopts rules enabling joint clinical assessments of medical devices and IVDs under the HTA Regulation.
EC Public Health · EU-wideEC Public Health publishes general principles governing AI use in preparing Joint Clinical Assessment dossiers.
EC Public Health · EU-wideUpdated guidance and eligibility tool published to support early information provision for joint clinical assessments under the EU HTA Regulation.
EC Public Health · EU-wideEuropean Commission invites input on the second joint action implementing the European Health Data Space framework.
EC Public Health · EU-wideProposal for an EU-wide Council Recommendation establishing a framework for cardiovascular health checks and early detection screening across member states.
EC Public Health · EU-wideUpdated guidance on methodology and procedure for joint clinical assessments under the EU HTA Regulation.
EC Public Health · EU-wideGuidance clarifying methodological and procedural requirements for joint clinical assessments under the EU HTA Regulation.
EC Public Health · EU-wideGuidance clarifying the proposed EU Recommendation on cardiovascular health screening and checks.
EC Public Health · EU-widePublication of guidance for sponsors on safety reporting procedures in combined clinical trials.
EC Public Health · EU-wideEC invites input on health hazards and risks posed by brain stimulation devices used outside medical contexts.
EC Public Health · EU-wideEuropean Commission invites organisations to join the EHDS Stakeholder Forum and Community to support implementation of the European Health Data Space.
EC Public Health · EU-wideThe European Medical Device Nomenclature (EMDN) is the nomenclature of use by manufacturers when registering their medical devices in the EUDAMED database. Founded on pre-established criteria and requirements and base...
EC Public Health · EU-wideEuropean Commission invites tenders for long-term API stockpiling and rapid finished-dose-form production capacity.
EC Public Health · EU-wideThe European Commission invites input on draft guidance for conducting clinical trials during public health emergencies.
EC Public Health · EU-wideUpdated Q&A guidance on safety features required for medicinal products for human use.
EC Public Health · EU-wideMember States' summaries of annual monitoring and on-site assessment reports for notified bodies under MDR and IVDR are now published.
EC Public Health · EU-wideNews announcement 13 July 2026 Updated list of notified bodies’ standard fees Updated list of notified bodies’ standard fees 1 min read
EC Public Health · EU-wideNews announcement 1 July 2026 June 2026 updated information on the applications for designation as a notified body - Overview of CABs/NBs at each stage of the designation process June 2026 updated information on the a...
EC Public Health · EU-wideNews announcement 8 May 2026 Update - Notified bodies survey on certifications and applications (8 May 2026) Update - Notified bodies survey on certifications and applications (8 May 2026) 1 min read
EC Public Health · EU-wideNews announcement 26 March 2026 Notified bodies survey on certifications and applications Notified bodies survey on certifications and applications 1 min read
EC Public Health · EU-wideThe European Commission has selected the first medical devices for joint clinical assessment under the HTA Regulation.
EC Public Health · EU-wideNews announcement 16 July 2026 Updated – Submission request template for medical devices 1 min read
EC Public Health · EU-wideNews announcement 6 March 2026 Overview of recommendations on preparedness and response to serious cross-border threats to health, pursuant to Article 7(2) of Regulation (EU) 2022/2371 Overview of recommendations on p...
EC Public Health · EU-wideNews announcement 7 April 2026 New publication of harmonised standards under the medical devices Regulation – April 2026 New publication of harmonised standards under the medical devices Regulation – April 2026 1 min ...
EC Public Health · EU-wideNews announcement 30 January 2026 New publications of harmonised standards under the medical devices Regulations – January 2026 New publications of harmonised standards under the medical devices Regulations – January ...
EC Public Health · EU-wideNews announcement 20 October 2025 New publication of Harmonised standards under the medical devices Regulations – October 2025 New publication of Harmonised standards under the medical devices Regulations – October 20...
EC Public Health · EU-wideSCHEER - Minutes of the Working Group Meeting on Brain stimulators of 29 September 2026
EC Public Health · EU-wideRegistration - European Biotech Clusters: Connect. Collaborate. Scale: Turning the Biotech Act’s ambition into action (19 November 2026)
EC Public Health · EU-wideThe European Commission invites evidence and public input on the evaluation of the Biocidal Products Regulation.
EC Public Health · EU-wideNews announcement 22 September 2026 HTA: New Opportunity to Apply for Joint Scientific Consultation 1 min read
EC Public Health · EU-wideEuropean Commission invites input on future priorities, orientations and needs for the EU4Health programme.
EC Public Health · EU-wideEuropean Commission invites final submissions to the Call for Evidence and public consultation on the Biocidal Products Regulation evaluation.
EC Public Health · EU-wideEuropean Commission procures €2.5 million in rapid molecular diagnostic tests for Bundibugyo Ebola outbreak response in DRC.
EC Public Health · EU-wideSummary report OECD/EUPHA - Long COVID Policy Dialogue
EC Public Health · EU-wideNew prevention toolkit to support children’s health and wellbeing
EC Public Health · EU-wideAgenda and registration - Prevention Toolkit for Children's Health and Well-being: the mental health chapter (9 October 2026)
EC Public Health · EU-wideExpert decision and opinion (CECP-EMA/EX/0000171363) - Orthopaedics, traumatology, rehabilitation, rheumatology
EC Public Health · EU-wideCommission launches EU Screening Week with new recommendations on cardiovascular health checks
EC Public Health · EU-wideExpert decision and opinion (CECP-EMA/EX/0000335537) - Orthopaedics, traumatology, rehabilitation, rheumatology
EC Public Health · EU-wideThe HTA Member State Coordination Group has adopted guiding principles on data transparency.
EC Public Health · EU-wideNews announcement 21 April 2026 Update - Member States-specific national requirements for clinical investigations and performance studies Update - Member States-specific national requirements for clinical investigatio...
EC Public Health · EU-wideNews announcement 7 January 2026 Health Technology Assessment: New opportunity to apply for Joint Scientific Consultations Health Technology Assessment: New opportunity to apply for Joint Scientific Consultations 1 mi...
EC Public Health · EU-wide