2nd Annual Software Design for Medical Devices Europe attendee directory


Pharmaceutical News

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Universität Münster

Uvo Hölscher, Professor, Medical Technology and Ergonomics

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Novo Nordisk GA&PP

Peter Bøge, Specialist

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Axon Lawyers

Erik Vollebregt, Partner

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Straumann

Andreas Petermann, Director Regulatory Affairs

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Medtronic Diabetes

Patty Krantz, CRDM Standards Advisor

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Siemens Healthcare

Markus Nagel, Director of Quality Management

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GE Healthcare

Paivi Roiha, Regulatory Affairs Leaders

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Given Imaging ProfEd

Iddo Ambor, Director, Software and Platforms

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Flextronics

Marco Rigamonti, Manager, Software Engineering Department

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TÜV SÜD AG

Markus Wagner, Lead Auditor, Quality Management Systems

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FDA Medical Devices

Molly Story, Human Factors and Accessible Medical Technology Specialist, Office of Device Evaluation, Center for Devices and Rad

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