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Session Chair(s)
J. Jason Lundy, PHD
Principal
Outcometrix, United States
Learning Objective : Describe the rationale for collecting patient-reported outcome (PRO) data electronically; Define conceptual equivalence testing and statistical equivalence testing; Discuss challenges to the use of ePRO instruments in clinical trials.
Speaker(s)
Panelist
Elektra Papadopoulos, MD, MPH
AbbVie, United States
Director, Patient Experience Data and Strategy
Panelist
David S. Reasner, PHD
FDA, United States
Director, Division of Clinical Outcome Assessment, OND, CDER
Panelist
Keith Wenzel
DIA Study Endpoints Community, United States
Volunteer
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