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.

Watch the Webinar View the Presentation

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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