Reporting the Unavailability of a Medical Device: Establishment of a European Procedure
21 Jul 2026
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IMDRF/SaMD WG/N81 FINAL: 2025: Characterization Considerations for Medical Device Software and Software-Specific Risk
21 Jul 2026
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Report a discontinuation or cessation of marketing of a medical device or an in vitro diagnostic medical device
21 Jul 2026
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Building Trust in AI Through a Cybersecurity Risk-Based Approach
21 Jul 2026
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Ministry of Health Publication: An Overview of Artificial Intelligence (AI) in Healthcare in France
21 Jul 2026
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REGULATION (EU) 2025/327 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of February 11, 2025, on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847
21 Jul 2026
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Submission of vigilance reports to Notified Bodies under the EU MDR and IVDR
21 Jul 2026
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New M.I.R. 7.3.1 Form – Mandatory Use Starting in November 2025
21 Jul 2026
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Eudamed Workshop
21 Jul 2026
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Launch of the MDSAP Platform: A Go-To Resource for Medical Device Manufacturers
21 Jul 2026
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MDCG 2025-6 – FAQ on the Interplay Between the MDR, the IVDR, and the Artificial Intelligence Act (AIA)
21 Jul 2026
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ISO 10993-1:2025 Biological evaluation of medical devices: New edition published on November 18, 2025
21 Jul 2026
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