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 in 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.
