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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.
Apply for an alternative conformity assessment route leading to Article 16(4) Certification.
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.