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    Clinical Data for Medical Devices

    Join us for a complimentary webinar in which we will discuss the Regulation (EU) 2017/745 with a special focus on the collection, generation and evaluation of clinical data for medical devices.
    Our expert, Dr. Kivia Pontes de Oliveira, will give you an insight on the following topics:

    • Requirements of the Regulation (EU) 2017/745 on clinical data
    • Identification of clinical data sources
    • Equivalence route and clinical investigation route
    • Post-Market Clinical Follow-up (PMCF) activities


    Booking has been disabled for this event. Please consider one of the alternative dates.

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