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    • Webinar
      Medical Devices

    Amending Regulation (EU) 2023-607 and possible pitfalls

    Providing a summary of the (EU) 2023/607 content and clarification around what are the responsibilities of manufacturers.

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    Impact of legacy devices of non-compliance with (EU) 2023/607 conditions

    The webinar will be useful to anyone involved in transitioning medical devices from the Directives (MDD/AIMDD) to the MDR in the EU.

    • EU 2023/607 and manufacturer’s responsibilities.

    • EU 2023/607 Non compliance NB Actions and consequences.

    • BSI implementation of EU 2023/607.

    • Process for transferring appropriate surveillance to BSI.

    Speakers

    Hear from the experts in this webinar

    Speaker

    Maddalena Pinsi

    Regulatory Lead, BSI
    Insights & Media

    Find out about the latest quality trends with insights from our experts

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