What is ePRO?
The only reliable method to collect subject self-reports and manage the data in real time
Benefits of ePRO
How ePRO improves data quality and trial management
FDA's PRO Draft Guidance
Draft Guidance supports the use of ePRO in clinical research
Return on Investment
Reduced data variance, smaller trials, improved safety and faster decisions
Regulatory Considerations
PHT ePRO system compliance with regulatory requirements
The Future of ePRO
Adaptive sample sizing, email alerts, ePRO-enabled cell phones, cognitive assessments and medication compliance
