戻る Agenda
eSource Symposium
Session Chair(s)
Chris Ramm
Clinical Ink, United States
A Common Tool for Investigator Site eSource (EHRS) Readiness Assessment
Learning Objective : Discuss the principles of risk-based approaches to successfully using esource clinical data; Identify how to implement a risk-based study monitoring approach to electronic clinical data; Describe methods to successfully assess electronic health records systems that will be used for clinical data.
Speaker(s)
A Common Tool for Investigator Site eSource (EHRS) Readiness Assessment
Catherine Celingant, MA
Pfizer Inc, United States
Executive Director, Data Monitoring and Management, Oncology Therapeutics Lead
Chris Ramm
Clinical Ink, United States
Time to Change the Clinical Trial Monitoring Paradigm: Results From Clinical Trials Using eSource and Risk-based Monitoring
Jules Mitchel, PHD, MBA
THI Pharma Services, United States
President and CEO