QMSR (Quality Management System Regulation): New FDA Regulation
21 Jul 2026
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Implementing Regulation (EU) 2026/977: The EU Harmonizes the Practices of Notified Bodies
21 Jul 2026
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Clinical Trials: Launch in France of a “fast-track” accelerated review process starting March 16, 2026
21 Jul 2026
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Switzerland: Registration of medical devices in swissdamed will be mandatory as of July 1, 2026
21 Jul 2026
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ISO 20417:2026 – What Changes Are in Store for the Information Provided by the Manufacturer?
21 Jul 2026
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Well-Established Technologies (WET): The European Commission publishes two delegated acts to ease certain requirements of Regulation (EU) 2017/745
21 Jul 2026
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NBCG-Med: Draft Guide on Managing Changes Under the MDR/IVDR
21 Jul 2026
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