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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
![Kei Torikai, MD, PhD](/_Images/member/Generic_Image_Missing-Profile.jpg)
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
![Sumito Ichimoto, MS](/_Images/member/Generic_Image_Missing-Profile.jpg)
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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