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Session 3 : Utilization of the J-PACMP system for Cell and Gene Therapy Products (Japanese)
Session Chair(s)
Teruyo Arato, PhD
Professor, Clinical Research and Medical Innovation Center
Hokkaido University Hospital, Japan
Ryutaro Hirasawa
CMC Regulatory Affairs, Manager
Daiichi Sankyo Co., Ltd., Japan
Speaker(s)
Jun Matsumoto
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Reviewer, Office of Biologics I
Yuriko Ishii
Daiichi Sankyo Co., Ltd, Japan
Associate Director, CMC Reguratory Affairs Department
Keigo Kawabe
Sumitomo Pharma Co.,Ltd., Japan
Quality Officer, Regenerative & Cellular Medicine Office
Naoyuki Hanada
Novartis Pharma K.K., Japan
Regulatory CMC
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