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This webinar focuses on preparing medical device and IVD stakeholders for the upcoming mandatory use of EUDAMED.
Designed to help organizations get ready for mandatory EUDAMED use and understand how it will impact their regulatory responsibilities.
The first four modules of EUDAMED that will become mandatory.
Key timelines leading up to and after May 2026.
Updates to BSI processes to align with EUDAMED requirements.
How certification supports digital transformation.
Associate Head of Medical Devices Notified Body
Regulatory Lead - Clinical Compliance
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