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  • January 31, 2017

    Bring Your Own Device (BYOD)

     This webinar provides an overview of scientific, logistical, and regulatory considerations when using a BYOD approach to collect patient-reported outcome data in clinical trials. Presenters: Jennifer Crager (YPrime) and Paul O’Donohoe, MS (CRF Health) PDF version...
  • October 27, 2016

    Ensuring Equivalence of Electronic and Paper Administration of Patient-Reported Outcome Measures

     This webinar provides an overview of scientific and regulatory considerations when migrating paper-based patient-reported outcome (PRO) measures to electronic modes of data collection. Presenters: Paul O’Donohoe, MS (CRF Health) and Willie Muehlhausen, DVM (ICON)...
  • October 27, 2016

    Ensuring Equivalence of Electronic and Paper Administration of Patient-Reported Outcome Measures

     This webinar provides an overview of scientific and regulatory considerations when migrating paper-based patient-reported outcome (PRO) measures to electronic modes of data collection. Presenters: Paul O’Donohoe, MS (CRF Health) and Willie Muehlhausen, DVM (ICON) PDF version...
  • May 18, 2016

    PRO Consortium Webinar: Methods for Determining Clinically Meaningful Change

     This webinar explores methodological approaches for determining whether changes observed in patient-reported outcome measures and other clinical outcome assessments are clinically meaningful. Moderator: Stacie Hudgens, MA (Clinical Outcome Solutions) Presenters: Joseph C. Cappelleri, PhD (Pfizer Inc.), Cheryl Coon, PhD (Outcometrix) and Kathy Wyrwich, PhD (Evidera)...
  • January 7, 2016

    Best Practices for ePRO Implementation in Clinical Trials

     This webinar provides an overview of considerations in selecting the optimal ePRO modes, review best practices related to the deployment of ePRO systems, and discuss key items for ePRO deployment in clinical trials. Presenters: Serge Bodart, MS (Biomedical Systems) and Elisa Holzbaur, BS, PMP (Almac) PDF version  ...
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  • CPAD - Critical Path For Alzheimer's Disease
  • TTC - Transplant Therapeutics Consortium
  • T1D - Type 1 Diabetes Consortium
  • HD-RSC - Huntington’s Disease Regulatory Science Consortium
  • RDCA-DAP - Rare Disease Cures Accelerator-Data and Analytics Platform
  • TOMI-T1D - Trial Outcome Markers Initiative in T1D
  • QuantMed - Quantitative Medicine Program
  • PredicTox KE - PredicTox Knowledge Environment
  • CDRC - CURE Drug Repurposing Collaboratory
  • SHIP-MD - System of Hospitals for Innovation in Pediatrics – Medical Devices
  • CPTA - Critical Path to Therapeutics for the Ataxias
  • CP-SCD - Critical Path for Sickle Cell Disease
  • RD-COA Consortium - Rare Disease Clinical Outcome Assessment Consortium
  • TRxA - Translational Therapeutics Accelerator
  • CP-RND - Critical Path for Rare Neurodegenerative Diseases
  • CPA-1 - Critical Path for Alpha-1 Antitrypsin Deficiency
  • CFAST - Coalition For Accelerating Standards and Therapies
  • BmDR - Biomarker Data Repository
  • CPP - Critical Path for Parkinson's
  • CPTR - Critical Path to TB Drug Regimens
  • DCC - Data Collaboration Center
  • D-RSC - Duchenne Regulatory Science Consortium
  • INC - International Neonatal Consortium
  • MSOAC - Multiple Sclerosis Outcome Assessments Consortium
  • PKD - Polycystic Kidney Disease Outcomes Consortium
  • PRO Consortium - Patient-Reported Outcome Consortium
  • eCOA Consortium - Electronic Clinical Outcome Assessment Consortium
  • PSTC - Predictive Safety Testing Consortium
  • PTC - Pediatric Trials Consortium
  • TB-PACTS - TB-Platform for Aggregation of Clinical TB Studies

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