Nexialist organized a webinar dedicated to Eudamed, the European medical device database.
The implementation of European regulations EU2017/745 MDR and EU2017/746 IVDR continues to raise questions for medical device manufacturers. For this reason, Nexialist, the consulting firm specializing in regulatory intelligence and compliance for healthcare products, recently organized a webinar on the subject and invited Ackomas to share its expertise.
The webinar featured a presentation of the European medical device database and an update on the deployment of Eudamed. Stéphane ANCEL, Business Manager at Ackomas, presented the KOA solution, which facilitates the publication of information in the Eudamed database.
The webinar is now available (French) for replay. If you too have questions about the Eudamed database, and would like to know how to achieve the required compliance, please don’t hesitate to contact us.
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