Registering medical devices on EUDAMED: operating mode & feedback from a manufacturer
Elem Ayne
Chloé Khalife Tognat
Poppy Abeto Kiesse
Valerio Gigante
Stéphane Ancel
Key Takeaways from the Webinar
Join our webinars to explore the latest regulatory compliance strategies in the medical device industry. Our experts provide practical solutions and answer your questions live.
Mastering UDI Structuring
Paragraph: Learn how to define and organize Basic UDI-DI, UDI-DI and UDI-PI for full traceability and compliance—straight from QA/RA experts and field engineers.
Real-World Pitfalls to Avoid
Paragraph: Discover the most common mistakes made by manufacturers during UDI submissions—and how to prevent them before they become regulatory risks.
Cross-Border Data Requirements
Paragraph: Understand how UDI expectations differ between Europe and other regions (e.g. GS1, GUDID) and how to align your data models globally.
Automation Makes the Difference
Paragraph: Manual data entry is no longer sustainable. Learn how machine-to-machine (M2M) integration reduces errors, speeds up validation, and secures submissions.
Expert Strategies from the Field
Paragraph: Hear first-hand from professionals leading EUDAMED implementation in their organizations—including medical device manufacturers and data managers.
A Timeline You Can’t Ignore
Paragraph: With full EUDAMED obligations approaching in 2025, this session outlines what to prioritize now to stay ahead—and audit-ready.
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