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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
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.
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The new transition timelines, which devices benefit from them and under what conditions.
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Which devices covered by expired MDD/AIMDD certificates can benefit from longer timelines.
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Abolishment of the sell-off provisions in the MDR and its impact.
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Transfer of appropriate surveillance from your Directive Notified Body to the MDR Notified Body.
Extension to the MDR transition timelines
Join this webinar to learn more about the proposal to extend the MDR transition timeline and how you can benefit from it.
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Dr Jayanth Katta, Head of UK Approved Body, Regulatory Services, BSI
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Suzanne Halliday, VP Regulatory, BSI
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