Director MR R&D Switzerland - Advanced Clinical Imaging Technology, Siemens Healthineers
Introduction
Session Title
Practical aspects of Medical Device Regulations and Approvals - R&D and radiology point of view
- Exemplify the FDA approval process through a concrete example
- Highlight the importance of regulatory roles from an R&D perspective
- Illustrate user perspective taking radiologists as an example
Biography
Since 2014
Director of “Advanced Clinical Imaging Technology”, the Siemens Healthineers MR Innovation Hub in Lausanne
2011-2014
Research engineer & collaboration manager Advanced Clinical Imaging Technology Lausanne
2007-2011
PhD in biomedical imaging at the EPF Lausanne
2001-2006
MSc in computer engineering (major “medical informatics”)
