Medrio

For sponsors, CROs and sites worldwide, Medrio aims to support efficient and secure clinical trials across pharmaceutical, biotech, medical device, and diagnostics. 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.

Medrio CDMS/EDC
The flagship product is a 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 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. Their 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 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.