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    • Webinar
      Medical Devices

    Article 16(4) Certification Scheme

    This webinar will discuss Article 16 MDR/IVDR and BSI’s Article 16(4) Certification Scheme.

    Key takeaways and learning objectives

    • Learn when an economic operator becomes a device manufacturer under Article 16/Art 10 obligations

    • Understand importer/distributor changes and Article 16(4) Certification requirements

    • Explore conditions for alternative conformity assessment routes for CE Marking compliance

    Speaker

    Presenter information

    Speaker

    Dr Albert Roossien

    Bert is a Regulatory Lead with BSI since 2017. He is co-responsible for the continued designation as a Medical Devices Notified Body.

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