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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)
Mutsukuni Kataoka
Sr. Director, Clinical Operations, IQVIA Services Japan K.K., Japan
Fact-Finding Survey on CRO Management for Site Monitoring Activity by CRO CRAs
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