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Jun 10 • 02 PM
Europe/Paris

Registering medical devices on EUDAMED: operating mode & feedback from a manufacturer

Legal manufacturers commercialize medical devices in Europe have entered the transitional year before Eudamed’s mandatory implementation in January 2026 for registering their products. This webinar provides an opportunity to review the operational procedures and associated standards. It is also an opportunity to get initial feedback from a manufacturer on the publication of these products via dedicated software.

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Duration
1h

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Don’t miss this expert panel on EUDAMED and regulatory practices.

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Elem Ayne

A blue flag with white and yellow stars arranged in a semi-circle on the left and the text "TEAM-PRRC" in large white letters on the right.

President of TEAM-PRRC, expert in QA/RA and PRRC support.

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Chloé Khalife Tognat

NovaSpine logo with a yellow circle containing a stylized white spine and the name "NovaSpine" in gray text to the right.

Quality Engineer at NOVASPINE, leading EUDAMED implementation.

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Poppy Abeto Kiesse

GS1 Austria logo with a blue circle featuring white curved lines and the text "GS1" in white and blue. "Austria" in orange sits below and right of the circle, representing trusted identification for medical devices and manufacturers.

Business Development Manager Healthcare, GS1 Austria.

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A woman wearing glasses and a black blazer, likely a manufacturer representative, smiles at the camera in a well-lit, blurred indoor setting—perfectly suited for discussions on EUDAMED compliance or medical devices.

Valerio Gigante

Regulatory Database Specialist – Southern Europe, Ackomas.

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Stéphane Ancel

Sales Manager, Ackomas – expert in healthcare data digitization.

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What You’ll Learn in This Webinar

Clarity on operational procedures

Learn which steps are expected and what tools are needed.

Learn from multiple stakeholders

From regulatory experts to manufacturer feedback – one event.

Free access

One hour of expert insights at no cost, online and direct.

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