Online Forum Roundtable: Regulatory Update for Medical Devices & In-vitro Diagnostics
Add to Calendar
When:
2. October 2025 @ 09:52 – 10:52
2025-10-02T09:52:00+02:00
2025-10-02T10:52:00+02:00
News and best practice from the following areas
Regulatory Affairs and Quality Management
for medical devices and IVD
Together with the cluster organizations Standortagentur Tirol, LISAvienna, Human.technology Styria, Medizintechnik-Cluster Oberösterreich, ecoplus Niederösterreich and Innovation Salzburg, we are once again expanding the regional “MDR Stammtische” into an Austria-wide online forum roundtable.
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
- 09:00 Updates from the federal states
Life Science Cluster Austria - 09:15 Regulatory Update: What can we expect in 2025?
Martin Schmid, Managing Director, en.co.tec - 09:35 Update DIGA reimbursement process Austria & status MDR-IVDR
Philipp Lindinger, Managing Director, AUSTROMED - 09:55 Research Use Only products in a legal context
Ruth Mahfoozpour, Head of Legal, Platomics GmbH - 10:15 Best Practice – Insights
Birgit Sebauer, Head of Quality and Regulatory Affairs, HARPS Europe Manufacturing GmbH
- 10:30 Q & A
Venue: ONLINE
The online forum is free of charge.
