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[V8-S5] Improving Clinical Operation and Data Quality - eSource Is Transforming Clinical Trials -
Session Chair(s)
Takuhiro Yamaguchi, PHD
Professor, Biostatistics, Tohoku University Graduate School of Medicine, Japan
ICT infrastructure is essential for the future clinical research and medical technology to provide scientific evidence. Project for Accelerating Medical Research through Cross-regional ICT Utilization is underway in Japan Agency for Medical Research and Development. The US FDA is driving the use of eSource. However, the adoption of eSource in clinical research has been delayed due to the difficulty of data manipulation. Data collection from eSource will be a more efficient way that will benefit patients, medical institutions and sponsors. In this session we will discuss challenges related to the use of eSource. We will also discuss how we can overcome them among industry, government and academia together.
Speaker(s)
Yasushi Matsumura, MD, PHD
Professor, Division of Medicine, Graduate School of Medicine, Osaka University, Japan
Direct Capture of Electronic Medical Record Data for Clinical Research
Yoshihiro Aoyagi, MS
Manager, Department of Medical Information, National Cancer Center Hospital East, Japan
Learning from EHR Data Utilization for Clinical Research / Clinical Trial
Tempei Miyaji, MSC
Project Assistant Professor, Department of Clinical Trial Data Management, The University of Tokyo, Japan
Challenges of Using Mobile in Clinical Research and Virtual Trial
Mika Ogasawara
Data Quality Lead, Biometrics and Data Management, Pfizer R&D Japan G.K., Japan
TransCelerate’s eSource Perspective