Medrio

Medrio combines configurable clinical trial platforms with services for study builds, data management, clinical reporting and database lock. Its software supports EDC, CTMS, eConsent, ePRO, eTMF, RTSM, analytics, integrations, and compliance workflows.

Clinical Trial Systems

• Run trial operations with Medrio CTMS for study planning, site management, monitoring reports, milestones, enrollment, quality metrics, and site payments.
• Capture participant and trial data through EDC, eConsent, and ePRO workflows with validated records, consent versioning, remote assessments, and endpoint collection.

Data Operations and Oversight

• Build and review study data with no-code eCRFs, edit checks, validation, continuous data review, dashboards, visualizations, and database-lock workflows.
• Connect devices, labs, analytics tools, and data warehouses through import, export, and API workflows for clinical and study metadata.

Randomization, Supply and Trial Documents

• Manage randomization, treatment allocation, kit assignment, inventory, expiry, resupply, and temperature-excursion notifications with configurable RTSM software.
• Maintain trial-document completeness with Medrio eTMF, powered by Engility, for filing, permissions, expiry tracking, and inspection-ready records.

Clinical Data Services

• Outsource data management or clinical reporting to Medrio experts for compliant study builds, eCRFs, databases, validations, and study-data support.
• Use Medrio services for data cleaning, database lock and audit-trail reviews aligned with regulated clinical research.

Best Fit

• Clinical teams needing configurable systems for data capture, consent, ePRO, trial management, supply, documents, and clinical data review.
• Sponsors and CROs seeking supplemental clinical data expertise for study builds, reporting, compliance workflows or database lock.