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  • Webinar
    Medical Devices

BSI’s Perspectives on Article 117 and Drug-Device Combinations

This webinar will focus on medical devices with ancillary medicinal substance and the conformity assessment process and key requirements.

In this webinar:

  • What is Article 117.

  • The process for DDC manufacturers.

  • Documentation requirements.

  • Output of the process.

BSI’s perspectives on Article 117 and drug-device combinations

Dr Jennifer Durrant and Dr Jonathan Sutch give their perspective on Article 117 and drug-device combination products.

Dr Jennifer Durrant, Global Head of Medicinal and Biologics, BSI

Dr Jonathan Sutch, Medicinal Technical Specialist, BSI

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