As part of this cross-cluster event, we would like to give you an insight into what to expect in 2027 regarding MDR-IVDR, MDCG and standards. As well as expert presentations and best practice examples, there will again be an opportunity to ask the experts and companies individual questions.
Program:
- 16:00 – Updates, LISA – Life Science Austria
- 16:15 – Regulatory Update: What to expect in 2027 regarding MDR-IVDR, MDCG and standards
Martin Schmid, en.co.tec - 16:40 – tbc
Monika Hupfauf, Attorney at Law and Christoph Dungl, B. Braun GmbH - 17:00 – From User Error to Managed Risk – How Usability Engineering and Risk Management Work Together
Michael Engler, EMPIANA GmbH - 17:20 – 10 Costly Supplier Mistakes: Test Method Validation and Process Validation
Simon Foeger, SIFo GmbH - 17:40 – Q & A
Registration is free of charge.