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    Brexit: What is the impact of the TCA on EU-UK Medical Device regulations?
    • Jan 7, 2021
    • 4 min

    Brexit: What is the impact of the TCA on EU-UK Medical Device regulations?

    MDR: key features to comply with language and translation requirements 6/6
    • Nov 26, 2020
    • 2 min

    MDR: key features to comply with language and translation requirements 6/6

    Les dispositifs médicaux et la FDA (3/3) : les alternatives à la 510(k) traditionnelle et à la APM
    • Nov 19, 2020
    • 3 min

    Les dispositifs médicaux et la FDA (3/3) : les alternatives à la 510(k) traditionnelle et à la APM

    Les dispositifs médicaux et la FDA (2/3) : GMPs/QSRs et ISO 13485
    • Nov 12, 2020
    • 3 min

    Les dispositifs médicaux et la FDA (2/3) : GMPs/QSRs et ISO 13485

    Les dispositifs médicaux et la FDA (1/3)
    • Oct 26, 2020
    • 4 min

    Les dispositifs médicaux et la FDA (1/3)

    MDR: The marketing and post-market surveillance phases (5/6)
    • Sep 17, 2020
    • 2 min

    MDR: The marketing and post-market surveillance phases (5/6)

    Connected Medical Devices To Necessitate Clinical Evaluation Requires MDR
    • May 25, 2020
    • 1 min

    Connected Medical Devices To Necessitate Clinical Evaluation Requires MDR

    Advertising your Medical Device in France: Use of Allegations and Comparisons
    • May 19, 2020
    • 2 min

    Advertising your Medical Device in France: Use of Allegations and Comparisons

    • May 5, 2020
    • 1 min

    Advertising your medical device in France during the state of health emergency

    The European Commission's guide on medical devices in the Covid-19 context
    • May 4, 2020
    • 1 min

    The European Commission's guide on medical devices in the Covid-19 context

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