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2016 年 03 月 03 日 9:30 上午 - 2016 年 03 月 04 日 5:00 下午

4th-DIA-Clinical-Operations-Monitoring-Workshop-in-Japan

PANEL DISCUSSION

Session Chair(s)

Suzuko  Oikawa, RPH

Suzuko Oikawa, RPH

Director, Clinical Research

Bristol-Myers Squibb, Japan

Ryosuke  Sakai

Ryosuke Sakai

Office of Non-clinical and Clinical Compliance

Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Kyoji  Tamanoi

Kyoji Tamanoi

Senior Clinical Trial Manager, Clinical Trial Management

ICON Japan K.K., Japan

Speaker(s)

Mutsukuni  Kataoka

Fact-Finding Survey on CRO Management for Site Monitoring Activity by CRO CRAs

Mutsukuni Kataoka

IQVIA Services Japan K.K., Japan

Sr. Director, Clinical Operations

Emi  Kozasa

Emi Kozasa

NEUES Co., Ltd., Japan

Takeyuki  Sato

Takeyuki Sato

Foundation for Biomedical Research and Innovation at Kobe, Japan

Advisor

Norio  Shimazaki

Norio Shimazaki

Bristol-Myers Squibb K.K., Japan

Director, Regional Clinical Operations Japan, Korea and Taiwan

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