• Post Market Surveys (PMCF/PMPF): Regulatory Framework and Best Practices

    Zoom Webinar
    Virtual Event
    Webinar | 17 September 2026 | 2:00 PM CET ABOUT THE WEBINAR Post-market surveys can be a practical, proportionate and scientifically robust tool for generating real-world evidence across the product lifecycle. This webinar will explore their application within Post-Market Clinical Follow-up (PMCF) and Post-Market Performance Follow-up (PMPF), providing an overview
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  • Clinical Evaluation for AI-Enabled Medical Device

    Zoom Webinar
    Virtual Event
    Navigating Clinical Evidence in the Age of AI Date: 14 October 2026 | Time: 17:00 CET / 16:00 GMTFormat: Online Webinar AI-enabled medical devices are reshaping the way we approach clinical evaluation. From defining sufficient clinical evidence to addressing bias, generalisability, evolving algorithms and real-world performance, these technologies bring new questions
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  • Introduction to In Silico and In Silico Clinical Trials, with Case Study Examples

    Zoom Webinar
    Virtual Event
    Discover how computational modelling and simulation can support clinical evidence generation for medical devices. 22 October 2026 | 2:00 PM CET | Online About the Webinar In silico methods are playing an increasingly important role in the way clinical evidence can be generated and assessed for medical devices. This webinar
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  • Live Q&A Session on the New ISO 18969 with Danielle Giroud

    Zoom Webinar
    Virtual Event
    Your Questions on the New Clinical Evaluation Standard — Answered by the ISO Working Group Convenor Date: 29 October 2026 | Time: 14:00 CET Format: Online Session (Zoom) The publication of ISO 18969, Clinical evaluation of medical devices, marks an important development for professionals involved in the clinical evaluation of
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