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An Explanation of the European Regulatory Requirements for Software (incl. specific examples of Imaging & Diagnostic Devices)
Mika Reinikainen, Managing Director, AbNovo Ltd |
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Standalone Software Products as Medical Devices: What Are They and What Are the Safety and Performance Issues?
Matthias Hölzer-Klüpfel, Independent Consultant |
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Technical Standards for Software
Dr. Andreas Purde, Department Manager, TÜV SÜD Product Service
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Software Validation - A Notified Body View
Werner Kexel, Managing Director Heath Care, BSI Health Care |
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Revolutionizing Medical Device Design
Julien Penders, Program Manager Body Area Networks, IMEC |
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The Changing Face of the Medical Field Courtesy of Wireless Technologies
Patrice Bertrand, Systems Architect Consumer and Industrial Segments, Freescale |
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Design a Medical Device Right the First Time - Perspective from a Certification Body
Hans-Werner Zeller, Manager Electro-Medical & Technology, Europe, CSA Group |
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Blindspots and Safer Medical Systems
Professor Harold Thimbleby, Director of the Future Interaction Technology Lab (FIT Lab) at Swansea University, Wales |
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Deriving Systems Requirements from Process Analysis
Prof. Dr.-Ing. Oliver Burgert, Medical Informatics, Reutlingen University, Germany |
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Leveraging Software Separation for Safe Medical Devices
Alan Johnson, Technology Director, Tactiq |
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User Interface Design Considerations
PD. Dr. med. Ulrich Matern, wwH-c GmbH |
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Pulse Oximetry System Design: Theory and Practice
Tom O'Dwyer, Director of Healthcare Technology, Analog Devices Inc. |
