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This webinar will discuss Article 16 MDR/IVDR and BSI’s Article 16(4) Certification Scheme.
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
Bert is a Regulatory Lead with BSI since 2017. He is co-responsible for the continued designation as a Medical Devices Notified Body.
Reach out and see how we can help guide you on your path to sustainable operational success.