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    • Webinar
      Medical Devices

    Extension to the MDR Transition Timelines

    Extension to the MDR transition timelines – impact on manufacturers and Notified Bodies

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    The EU Commission proposal to extend the MDR transition timelines

    Anyone involved in transitioning medical devices from the Directives (MDD/AIMDD) to the MDR in the EU.

    • The new transition timelines, which devices benefit from them and under what conditions.

    • Which devices covered by expired MDD/AIMDD certificates can benefit from longer timelines.

    • Abolishment of the sell-off provisions in the MDR and its impact.

    • Transfer of appropriate surveillance from your Directive Notified Body to the MDR Notified Body.

    Speakers

    Hear from the experts in this webinar

    Speaker

    Dr Jayanth Katta

    Head of UK Approved Body, Regulatory Services, BSI
    Speaker

    Suzanne Halliday

    VP, Regulatory Services, BSI
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