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[V3-S2] Technical and Operational Know-How for Conducting Clinical Studies under Limited Manpower
Session Chair(s)
![Chie Sakanaka, MD, PhD](/_Images/member/Generic_Image_Missing-Profile.jpg)
Chie Sakanaka, MD, PhD
Vice Director, Associate Professor, Clinical Research Support Center
The University of Tokyo Hospital, Japan
This session will provide you with a forum of hints and tips for efficient operation in clinical studies in order to overcome issues and prepare for risks during the operation. To contribute to development of innovative NCE/NBEs and medical devices, cooperation among the 3 stakeholders, academia, government agencies and pharma companies are necessary. Especially, under constraints of resources, not only efficient use of time but also efficient process designs such as staff specialization and reporting/submission are required. As we are in the middle of rapid globalization, input from a speaker outside Japan will contribute to the discussions.
Speaker(s)
Challenges in Conducting Clinical Trials
Jie Willey, MSN
University of Texas, MD Anderson Cancer Center, United States
Administrative Director, Protocol Research
![Shinobu Shimizu, PhD](/_Images/member/Generic_Image_Missing-Profile.jpg)
Toward Implementation of Investigator-Initiated Clinical Trial in Academia
Shinobu Shimizu, PhD
Nagoya Univeresity Hospital, Japan
Associate Professor, Department of Advanced Medicine
![Souta Mizumoto, MPharm, MSc](/_Images/member/Generic_Image_Missing-Profile.jpg)
How Lilly Japan Applied Six Sigma to Improve Productivity
Souta Mizumoto, MPharm, MSc
Eli Lilly Japan K.K., Japan
Director, Global Patient Safety-Japan; Six Sigma Champion
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