Product Overview
Not all ePRO is created equal. To ensure you get the most accurate outcomes possible, you need ePRO designed by digital experts—and purpose-built for ease.
- Ease: Easier, less burdensome reporting for participants results in higher compliance.
- Real-Time, Real Life: Real-time reporting of real-life data delivers more accurate and complete data sets.
- Accuracy: More accurate and complete data sets result in better, more reliable outcomes.
- Retention: Lower dropout rates reduce the sample sizes required to power your study.
Today’s ePRO offerings are too often digitized versions of poor traditional assessments. Upgrade your clinical trial with ObvioHealth’s ePRO—purpose-built for digital and designed to deliver better data, faster.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
- Our BYOD ePRO model integrates seamlessly into patients’ lives, allowing them to report using their own mobile devices.
- Our patient experience is specifically designed for ease, with user-friendly scales and interactive functions that make data capture quick and intuitive.
- Automated alerts, notifications, and reminders are built in to boost compliance, keeping participants engaged from start to finish.
About the company
ObvioHealth is transforming the clinical trial landscape with cutting-edge digital solutions. Our ObvioGo® 2.0 platform streamlines study design, enhances data accuracy, and improves participant engagement, driving faster and more reliable research outcomes. Experience the next generation of clinical trials with our innovative approach, delivering accurate data for sponsors and an improved experience for participants and sites.
ObvioHealth’s unique model combines advanced digital tools with best-practice clinical science to create a fully integrated platform. Our ObvioGo® app ensures high participant engagement and data accuracy, while the Study Designer empowers teams to efficiently create and customize trials. The Study Manager centralizes and simplifies trial management, optimizing workflows and ensuring real-time compliance. This comprehensive approach allows us to deliver robust therapeutic evidence and a seamless experience for sponsors and participants alike.
