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Overview
Advanced registraion has been closed.
Please come to the on-site Registration Desk if you would like to attend.
This symposium will be conducted in Japanese Language.
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Program Committee
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Keiko Tsumori, MSc Associate Director, Medical Writing, Regulatory Affairs Area, Japan Development
MSD K.K., Japan -
Yuko Kojima, RPh Sr. Executive Director
Eli Lilly Japan K.K., Japan -
Rika Abe, RPh Research Administrator, Office of the Fugaku Society 5.0 Initiative
RIKEN Center for Computational Science, Japan -
Yasufumi Kuroda, PhD Associate Director, PV Dept.
Daiichi Sankyo Company, Limited, Japan -
Hiroki Nagahama, MS Manager, Safety Evaluation & Risk Management Dept.,
GlaxoSmithKline K.K., Japan -
Shohko Sekine Reviewer, Office of New Drug IV
Pharmaceuticals and Medical Devices Agency (PMDA), Japan -
Naoko Tejima Group Manager, Regulatory Writing & Operations Group, Regulatory Affairs
Astellas Amgen Biopharma, Japan -
Seiki Yamazaki Director, Clinical Informatics & Innovation
Pfizer Japan Inc., Japan -
Hideo Nakada, RPh Deputy Associate Manager, Department of Hospital Pharmacy
Keio University, Japan
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