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Session 4 : Digitalization of protocols for clinical trials and Data flow
Session Chair(s)
Fumiharu Tanaka, MPharm, RPh
Manager, Clinical Operation, SHIONOGI & CO., LTD., Japan
Miho Tabata
Chief Reviewer, Office of generic Drugs, Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Speaker(s)
Collaboration to Unlock Innovation: How Digitized Protocols Can Transform Data Flow Automation in Clinical Trial
Mika Ogasawara
Data Quality Lead, Biometrics and Data Management, Pfizer R&D Japan G.K., Japan
Connecting Electronic Health Records and EDC Through a Digital Protocol: Toward a Sustainable Data Utilization Ecosystem
Keiko Ota
Center for Clinical Research and Innovation, Osaka Metropolitan University Hospital, Ehime University, Japan
Optimization of Clinical Trial Operations Through Electronic Medical Record Data Utilization -Current Status and Future Outlook -
Rie Taniguchi
CRC, Clinical Research Coordinating Section, National Cancer Center Hospital East, Japan
DataTransferofElectricHealthRecordtoEDC - Insights under Global Regulations -
Eri Sekine
Executive Vice President Data Business and Quality, CMIC Co., Ltd, Japan
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