Online Forum Roundtable: Regulatory Update for Medical Devices & In-vitro Diagnostics
News and best practice from the following areas
Regulatory Affairs and Quality Management
for medical devices and IVD

In this cross-cluster event, we would like to give you a regulatory update on specific topics of the MDR-IVDR.
In addition to the expert presentations and practical examples, there will again be an opportunity for individual questions afterwards!
Program
- 16:00 Updates from the federal states
Life Science Cluster Austria - 16:10 Regulatory Update
Martin Schmid, en.co.tec - 16:20 Funding meets regulation: building bridges for DeepTech innovations
Regina Weinmüllner, AWS - 16:45 Best Practice: Lines of Code, Layers of Regulation – ESD’s path to MDR certification
Yvonne Rauner, ESD - 17:10 tbc
- 17:40 Q & A
- more program details will follow soon!
Venue: ONLINE
The online forum is free of charge.
