The volume of data collected in clinical trials has increased significantly, offering invaluable insights into disease understanding, data accuracy, and safety monitoring. However, it can place a heavy burden on patients responsible for self-reporting.

Selecting the right electronic Patient-Reported Outcomes (ePRO) tool is critical to balancing comprehensive data collection with a good patient experience. That’s why we developed a concise guide that provides you with five essential aspects to consider when evaluating ePRO tools for your clinical study.

With over a decade of experience in clinical trial support, our expert insights will help you navigate the complexities of ePRO selection effectively. This checklist features practical advice with questions to ask during your evaluation.