- Search BSI
- Verify a Certificate
Suggested region and language based on your location
Your current region and language
This webinar will focus on medical devices with ancillary medicinal substance and the conformity assessment process and key requirements.
What is Article 117.
The process for DDC manufacturers.
Documentation requirements.
Output of the process.
Global Head of Medicinal and Biologics, BSI
Medicinal Technical Specialist, BSI
Reach out and see how we can help guide you on your path to sustainable operational success.