The timetable for the implementation of regulations EU 2017/745 and EU 2017/746 continues to unfold, with an important next step: the operational qualification of the EUDAMED database. This step, which makes mandatory the publication of data on Medical Devices and In Vitro Diagnostics, still raises many questions among industry professionals.
Ackomas is organizing a webinar for medical device manufacturers and consulting firms, in association with GS1 France, which will address the standards adopted by the European Commission for article identification (UDI), in order to clear up any grey areas and address the various practical issues surrounding EUDAMED compliance.
This webinar will focus on information and exchange, covering the following topics:
- How do you code your articles?
- What are the practical aspects of publication?
- How do you ensure EUDAMED compliance?
- How to control the process?
To attend this webinar presented by Stéphane ANCEL, Ackomas Sales Director, and Laurence Azoulay, GS1 France Santé & Cosmétique, simply register by clicking on the following button.
Themes
