Electronic IFU: Summary of the Amendments Made by Regulation (EU) 2025/1234 to Implementing Regulation (EU) 2021/2226
21 Jul 2026
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MDR – Language Requirements for Manufacturers – Rev. 3 (August 2025)
21 Jul 2026
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EUDAMED: Update on Decision (EU) 2025/2371 of November 26, 2025
21 Jul 2026
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Proposed Amendments to the MDR and IVDR Regulations
21 Jul 2026
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Contribution from Team NB – Revision of the DM and DMDIV Regulations
21 Jul 2026
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MDCG 2025-10 Guidance on Postmarket Surveillance of Medical Devices and In Vitro Diagnostic Medical Devices
21 Jul 2026
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QMSR: The FDA Clarifies Its Expectations Ahead of the New Regulation’s Effective Date
21 Jul 2026
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📢Update to the harmonized standards under Regulation (EU) 2017/745
21 Jul 2026
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Recertification Under the MDR and IVDR – Frequently Asked Questions
21 Jul 2026
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Update to the MDSAP Audit Approach (MDSAP AU P0002.010)
21 Jul 2026
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Delegated Regulation (EU) C(2026)1798: Expansion of Devices Exempt from Clinical Investigations
21 Jul 2026
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ISO 14155:2026: Updates to the Standard on Clinical Investigations of Medical Devices
21 Jul 2026
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