eCOA 101: Why Choose ePRO vs. Paper

Electronic patient-reported outcome (ePRO) solutions are revolutionizing clinical trials by enhancing data quality, operational efficiency, and patient-centricity. These digital tools improve data quality, reliability, and integrity by preventing missing or conflicting entries, ensuring timely assessments, minimizing recall bias, and providing an audit trail for transparency. Investigators benefit from real-time access to patient data, enabling better monitoring and timely follow-ups.

Explore how ePRO reduces the burden on clinical sites, leading to increased statistical power while complying with FDA and Good Clinical Practice (GCP) requirements.