Topic 1
Further information
The online info event is devided into two parts:
- In the first half, University Professor Folker Spitzenberger of TH Lübeck and industry expert Philippe Etter of Medidee share their theoretical and practical insights about the new European regulatory framework for medical devices (Regulation
(EU) 2017/745 on medical devices - „MDR“ - and Regulation (EU) 2017/746 on in vitro diagnostic medical devices - „IVDR“) which leads to numerous consequences for all stakeholders of the medical device sector.
- In the second half, you will be introduced to the certified high-level training in clinical, regulatory, and quality affairs for medical devices and in-vitro diagnostic medical devices: CARAQA.
- In the first half, University Professor Folker Spitzenberger of TH Lübeck and industry expert Philippe Etter of Medidee share their theoretical and practical insights about the new European regulatory framework for medical devices (Regulation
(EU) 2017/745 on medical devices - „MDR“ - and Regulation (EU) 2017/746 on in vitro diagnostic medical devices - „IVDR“) which leads to numerous consequences for all stakeholders of the medical device sector.
