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[V4-S6] The Challenges and Future Expectations of Postmarketing Registry System for New Medical Devices in Cooperation with Industry/PMDA/Academia
Session Chair(s)
Tomiko Tawaragi
Chief Director
RAD-AR, Japan
TBC
Speaker(s)
Medical Device Registry and Post-Marketing Surveillance - Past Experience and Future Regulatory Challenges
Kensuke Ishii, PhD
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Director, Office of Medical Devices I
Benefit and Issues to Be Resolved of Medical Device Registry - Academia Perspective
Haruko Yamamoto, MD, PhD
National Cerebral and Cardiovascular Center, Japan
Director, Department of Data Science
The Current Status and Future Perspective of TAVI Registry
Kei Torikai, MD, PhD
Osaka University Graduate School of Medicine, Japan
Assistant Professor, Department of Cardiovascular Surgery
Development of Medical Device Registry for Post-Marketing Surveillance - Industry Perspective
Sumito Ichimoto, MS
Covidien Japan Inc., Japan
Director, Regulatory Affairs & Clinical Development, NeuroVascular
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