Tobias Kober

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”)