Poster: Test-Retest Reliability and Equivalence of PRO Measures
Poster: Equivalence of Electronic and Paper Administration of PRO
Poster: Spirometer and eDiary Integration for Asthma Trials
Equivalence of Electronic and Paper Administration of Patient-Reported Outcome Measures: 2007-2013
Capturing Patient-Reported Outcome (PRO) Data Electronically: The Past, Present, and Promise of ePRO Measurement in Clinical Trials
Putting the Oncology Patient First
Developing an eCOA Device Supply Strategy: The Vital Considerations for a Global Clinical Trial
What the Future Holds for Informed Consent
Case Study: World's Largest COPD eCOA Trial Requires Reliability and Global Scale
ePRO vs. Paper: Applied Clinical Trials
Managing ePRO Patient Compliance in Emerging Markets
Patient Compliance, ePRO and the Role of the Caregiver
Poster: eCOA Best Practices in Diabetes Clinical Trials
Recruitment & Retention: Breaking Down the Barriers to eConsent Adoption
In Pursuit of eConsent: Best Practice Recommendations for Successful Integration
ePRO: Enhancing Patient Compliance and Product Safety
Guidance for Industry Patient-Reported Outcome Measures: Use in Medical Product Development to Support Labeling Claims
Recommendations on Evidence Needed to Support Measurement Equivalence between Electronic and Paper-based Patient-Reported Outcome (PRO) Measures: ISPOR ePRO Good Research Practices
ePRO Helps Sponsors Deliver a More Patient-Centric Study
Case Study: TrialMax® Makes Infusion Data Capture Easier in Rare Disease Studies