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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
Director, RAD-AR Council, Japan
TBC
Speaker(s)
Kensuke Ishii, PHD
Director, Office of Medical Devices I, Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Medical Device Registry and Post-Marketing Surveillance - Past Experience and Future Regulatory Challenges
Haruko Yamamoto, MD, PHD
Executive Director, National Cerebral and Cardiovascular Center, Japan
Benefit and Issues to Be Resolved of Medical Device Registry - Academia Perspective
Kei Torikai, MD, PHD
Assistant Professor, Department of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Japan
The Current Status and Future Perspective of TAVI Registry
Sumito Ichimoto, MS
Director, Regulatory Affairs & Clinical Development, NeuroVascular, Covidien Japan Inc., Japan
Development of Medical Device Registry for Post-Marketing Surveillance - Industry Perspective
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