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Market surveillance and vigilance - Public Health

    https://health.ec.europa.eu/medical-devices-sector/directives/market-surveillance-and-vigilance_en
    The enforcement of the harmonised legislation on medical devices is the responsibility of the authorities in EU countries. The Medical Devices Directives establish specific procedures that the national authorities must follow when considering whether or not: 1. a medical device is unsafe and … See more

4th Annual European Medical Device & Diagnostic Post …

    https://www.iqvia.com/events/2022/10/4th-annual-european-medical-device-diagnostic-post-market-proactive-surveillance
    The 4th Annual European Medical Device and Diagnostic Post-Market Proactive Surveillance and Vigilance Conference is an interactive knowledge-sharing …

5 Postmarket Surveillance System Musts for Every EU …

    https://www.greenlight.guru/blog/postmarket-surveillance-system-eu
    Postmarket surveillance plan. A postmarket surveillance plan is a systematic …

Post Market Surveillance System – The European Union …

    https://eumdr.com/post-market-surveillance-system/
    detect reportable trends, update the technical documentation, identify necessary preventive, corrective or field safety corrective action, identify opportunities to improve the usability, …

Post-Market Surveillance for EU MDR - QualityMedDev

    https://www.qualitymeddev.com/2020/10/25/post-market-surveillance-eu-mdr/
    Post-Market Surveillance Procedure. QualityMedDev provides a Post-Market Surveillance Procedure that defines all the …



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