Hybrid and DCT studies are becoming an increasingly common part of modern clinical research. ePRO is designed to support both scenarios. Participants receive an invitation via automated emails to complete a questionnaire, after which their responses are securely and immediately stored in the study’s eCRF.

Filling out questionnaires takes time and effort on the part of participants, which can affect their motivation and, consequently, the reliability of the dataset. ePRO lowers the barrier to participation and reduces the risk of unreliable data by providing a user-friendly, intuitive environment.

• Available anytime, anywhere: Participants complete questionnaires on their own devices and at their own convenience.
• Intuitive interface: encourages correct input and minimizes input errors.
• Automatic reminders: Participants are reminded to complete questionnaires on time, without the research team having to follow up.
• Real-time reporting: Participants report in real time, rather than relying on their memory afterward, which increases the likelihood of accurate and complete data.

ePRO provides real-time insight into participants who are falling behind, progress by site, and patterns in the data, enabling proactive adjustments and monitoring of data quality. Data exports also offer additional insight for monitoring and reporting. Furthermore, every action is recorded in an audit trail, ensuring that data is always accurate and fully traceable.