Related Posts

• 
  Optimizing Electronic Capture of Clinical Outcome Assessment Data in Clinical Trials: The Case of Patient-Reported Endpoints
• 
  “Bring Your Own Device” (BYOD): The Future of Field-Based Patient-Reported Outcome Data Collection in Clinical Trials?
• 
  Considerations for Requiring Subjects to Provide a Response to Electronic Patient-Reported Outcome Instruments
• 
  ePRO Systems Validation: Clearly Defining The Roles Of Clinical Trial Teams And ePRO System Providers
• 
  Critical Path Institute’s Electronic Patient-Reported Outcome Consortium