Quality Management
The ICCAS maintains a quality management system according to DIN EN ISO 13485:2021 with the scope “research and development work of medical device software”. The quality management is led by the representative Johann Berger and in deputy by Dr. Stefan Bohn.
The responsible person according to Art. 15 MDR (“Person Responsible for Regulatory Compliance”) is Erik Schreiber.
Dr. Alexander Oeser is medical device consultant for the product KAIT and Jan Gaebel is medical device consultant for the product EOS (RescEU).
Directorate
Johann Berger
Image-guided Focused Ultrasound, Digital Patient Model
E-Mail: johann.berger@medizin.uni-leipzig.de
Dr.-Ing. Stefan Bohn
MODEL-BASED AUTOMATION AND INTEGRATION
E-Mail: Stefan.Bohn@medizin.uni-leipzig.de
Christoph Georgi
Model-Based Automation and Integration
E-Mail: christoph.georgi@medizin.uni-leipzig.de
Dr. Alexander Oeser
Digital Patient Model
E-Mail: alexander.oeser@medizin.uni-leipzig.de
Tobias Pabst
Model-Based Automation and Integration
E-Mail: tobias.pabst@medizin.uni-leipzig.de
Anna Schatz
Model-Based Automation and Integration
E-Mail: anna.schatz@medizin.uni-leipzig.de
Erik Schreiber
Model-Based Automation and Integration
E-Mail: erik.schreiber@medizin.uni-leipzig.de