Access the full recording and discover key strategies for achieving successful regulatory compliance.

Profitez de ce webinaire gratuit pour apprendre comment simplifier et accélérer votre conformité EUDAMED.

The project accelerates the EUDAMED rollout by allowing module-based qualification. The ACTOR, UDI, and CERTIFICATE modules could become mandatory by the end of 2025. During the March 5, 2024 webinar, Stéphane Ancel (ACKOMAS) and Arnaud Augris (SNITEM) presented the impacts for manufacturers, who will have less than two years to comply. Over 300 participants attended the session.

Nexialist is organizing a webinar dedicated to Eudamed, the European medical device database.

The implementation of European regulations EU2017/745 MDR and EU2017/746 IVDR still raises so many questions for medical device manufacturers. For this reason, Nexialist, the consulting firm specializing in regulatory intelligence and compliance for health products, recently organized a webinar on the subject and invited Ackomas to share his expertise.

On the program for this webinar, a presentation of the European medical device database and an overview of the deployment of Eudamed. Stéphane ANCEL, Business Manager at Ackomas, notably presented the KOA solution which facilitates the publication of information in the Eudamed database.

The webinar is now available for replay. If you also have questions about the Eudamed database and would like to know how to achieve the required compliance, do not hesitate to contact us.