Empowers participants and clinicians with convenient, accurate electronic outcome reporting for clinical trials, enhancing data quality and study efficiency.
Vendor
Medrio
Company Website
The eCOA/ePRO Solution from Medrio is designed to empower participants, clinicians, and observers in clinical trials by enabling convenient and accurate outcome reporting. This electronic patient-reported outcomes (ePRO) and electronic clinical outcome assessments (eCOA) software enhances data quality and study efficiency. It increases participant engagement through a web-based, device-agnostic interface, making participation easy. The solution supports complex protocols by allowing data collection in-clinic or remotely, utilizing validated and home-grown surveys. Crucially, it provides real-time access to clinical data, allowing for immediate decisions with no delay between collection and monitoring. The software features an intuitive, configurable interface built to improve the participant experience, site processes, and data quality throughout the trial lifecycle. It aims to demonstrate value to regulators and payors with high-quality data, improved participant compliance, and retention through an easy-to-use interface, automated notifications, and the MyMedrio participant portal. The solution can accelerate study startup, with setup in as little as four weeks, reducing costs and ensuring adherence to study timelines and industry standards. Medrio boasts a 98% customer retention rate, indicating high satisfaction with its integrated suite of solutions, which includes CDMS/EDC, eConsent, RTSM, Clinical Data Services, and Clinical Trial Project Management.
Features & Benefits
- Increased Participant Engagement: Web-based, device-agnostic solution makes participation easy and improves compliance and retention.
- Support for Complex Protocols: Collect data in-clinic or remotely with validated and home-grown surveys.
- Real-Time Data Access: View data instantly to make real-time decisions with zero delays.
- Accelerated Study Startup: Set up in as little as four weeks, reducing costs and accelerating data capture.
- High-Quality Data for Evidence: Demonstrate value to regulators and payors with accurate, reliable data.