Medrio
Trusted by sponsors, CROs and sites worldwide, Medrio aims to improve 100 million lives through faster, more efficient, and secure clinical trials. With almost two decades of experience, Medrio delivers proven, scalable solutions, unrivaled customer support, and guidance to the industry’s leading innovators, including pharmaceutical, biotech, medical device, diagnostics and more. The company’s suite of solutions, including CDMS/EDC, eCOA/ePRO, eConsent and RTSM, enables the capture of quality clinical trial data while optimizing workflows for regulatory readiness. Experience the power of Medrio and realize the full potential of your clinical operations and outcomes.
From traditional to fully decentralized clinical trials, Medrio's suite of solutions is flexible and configurable to meet the needs of any clinical trial. Our solutions are easy to learn, easy to use, scalable and connected through one unified platform, providing unmatched efficiency, clarity and sophistication:
Medrio CDMS/EDC
Our flagship product is a user-friendly clinical data management solution (CDMS) streamlining clinical electronic data collection and management in clinical trials. More than just a data collection tool, Medrio CDMS/EDC combines an intuitive user interface, seamless on and offline data capture capabilities, and comprehensive study data management in a single platform.
Medrio eCOA/ePRO
Medrio eCOA/ePRO is a web-based solution for collecting clinical outcome assessments (COAs), which measure the change in a clinical outcome. Medrio eCOA/ePRO supports patient-reported outcome (PRO) measures, clinician-reported outcome (ClinRO) measures and observer-reported outcome (ObsRO) measures. Our BYOD approach ensures participants respond to surveys anywhere at any time, and automated notifications ensure compliance while boosting retention and engagement. Medrio's unified eCOA/ePRO and CDMS solution allows users to view all COAs in one place.
Medrio eConsent
Medrio eConsent is a web-based tool for delivering consent forms, capturing electronic signatures, and supporting workflows such as in-clinic, remote, and self-registration consent. It accommodates multiple signers and allows for the upload of paper consent forms. Medrio eConsent also provides a dashboard for tracking participant consent statuses and supports complex hybrid workflows within a study.
Medrio RTSM
Medrio RTSM provides comprehensive randomization and trial supply management capabilities, ensuring accurate allocation of treatment assignments and efficient inventory control. RTSM is primarily used in double-blind, randomized controlled trials to evaluate an investigatory product's safety and efficacy.
Discover how Medrio's eClinical solutions deliver speed, simplicity, and quality for your trials with precisely what you need. Let our experts show you how to streamline your studies, reduce data entry errors, and accelerate your trials.
