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PANEL DISCUSSION
Session Chair(s)
Suzuko Oikawa, RPh
Director, Clinical Research, Bristol-Myers Squibb, Japan
Ryosuke Sakai
Office of Non-clinical and Clinical Compliance, Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Kyoji Tamanoi
Senior Clinical Trial Manager, Clinical Trial Management, ICON Japan K.K., Japan
Speaker(s)
Fact-Finding Survey on CRO Management for Site Monitoring Activity by CRO CRAs
Mutsukuni Kataoka
Sr. Director, Clinical Operations, IQVIA Services Japan K.K., Japan
Emi Kozasa
, NEUES Co., Ltd., Japan
Takeyuki Sato
Advisor, Foundation for Biomedical Research and Innovation at Kobe, Japan
Norio Shimazaki
Director, Regional Clinical Operations Japan, Korea and Taiwan, Bristol-Myers Squibb K.K., Japan
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