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PRO Data Collection in Clinical Trials Using Mixed Modes

PRO Data Collection in Clinical Trials Using Mixed Modes: Report of the ISPOR PRO Mixed Modes Good Research Practices Task Force

The citation for this report is: 
Eremenco S, Coons SJ, Paty, J, et al. PRO data collection in clinical trials using mixed modes: Report of the ISPOR PRO mixed modes good research practices task force. Value Health 2014;17:501 – 516.

Editorial: Review of the Task Force Report on PRO Data Collection in Clinical Trials Using Mixed Modes

Lori McLeod, PhD, RTI Health Solutions, Research Triangle Park, NC, USA

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Leadership Group
Sonya Eremenco, MA, Director, ePRO New Products, Evidera Bethesda, MD, USA
Stephen Joel Coons, PhD, Executive Director, Patient-Reported Outcome Consortium, Critical Path Institute, Tucson, AZ, USA
Karin Coyne, PhD, Scientific Director, Center for Health Outcomes Research, United BioSource Corporation, Bethesda, MD, USA
Damian McEntegart, BSc, Senior Director Statistics & ePRO Support, Perceptive Informatics, Nottingham, England, UK
Jean Paty, PhD, Chief Scientist and Regulatory Advisor - Outcomes, ERT, Inc., Pittsburgh, PA, USA

Final Report 
The task force sent out drafts for review twice during the development process and received comments on work to date during two ISPOR Forums.  The task force appreciates the written comments received from reviewers.  All comments, many of which were substantive, were read and addressed as appropriate.  Participation as reviewer by ISPOR members contributes to the high quality, expert consensus nature of these scientific guidance reports.

ISPOR Good Practices For Outcomes Research Index