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Bring Your Own Device (BYOD) Approaches to the Collection of Electronic Patient-Reported Outcome Data in Clinical Trials
Session Chair(s)
Chad Gwaltney, PhD
President
Gwaltney Consulting, United States
Bring Your Own Device (BYOD) approaches allow study subjects to use their personal digital devices to complete remote (i.e., offsite) patient-reported outcome measures. This session will describe key scientific, regulatory, and operational considerations when using BYOD.
Learning Objective : Compare the principles of Bring Your Own Device (BYOD) methodologies in clinical trials approaches using dedicated devices provided by study sites; Describe the operational features of a BYOD methodology; Identify the key scientific and regulatory considerations regarding BYOD in preapproval and postapproval research.
Speaker(s)
Strengths of BYOD Approaches
Chris David Watson, PhD
ERT, United Kingdom
Director of Product Strategy - Digital Patient
Challenges Associated with BYOD
Paul O'Donohoe, MS, MSc
Medidata Solutions, United States
Senior Director, eCOA Product and Science
Open Scientific, Regulatory, and Operational Questions Regarding BYOD
Stephen Joel Coons, PhD
Critical Path Institute, United States
Senior Advisor
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