News & Events

• February 28, 2017
  

  Considerations for Requiring Subjects to Respond to PRO Instruments Collected Electronically

  This webinar provides an overview of specific considerations related to allowing subjects to opt out of responding to individual items when PRO data collection is electronic as well as the relevance to other types of electronic clinical outcome assessments. Presenters: Paul O’Donohoe, MS (CRF Health) and Sonya Eremenco, MA (C-Path) PDF version...
• 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) PDF version...
• 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  ...
• May 6, 2015
  

  Migrating a PRO Instrument

  This webinar provides a detailed description of the process for conducting paper to ePRO migration, mode-specific migrations, usability, feasibility and user acceptance testing as well as case studies of successful migrations. Presenters: Serge Bodart, MSc (Biomedical Systems) Alisandra Johnson, BS (Bracket) PDF version  ...