Medrio is a leading provider of cloud-based clinical trial software solutions that streamline data capture, management, and regulatory compliance for life sciences organizations. Their unified platform supports electronic data capture (EDC), eConsent, eCOA/ePRO, randomization and trial supply management (RTSM), and decentralized clinical trial (DCT) capabilities, empowering pharmaceutical, biotech, medtech, and animal health innovators to accelerate and optimize clinical research.
Vendor
Medrio
Company Website
- Electronic Consent (eConsent)
Streamlines informed consent in clinical trials, enabling remote and onsite participation with compliance and enhanced comprehension.
- Electronic Patient-Reported Outcome (ePRO)
Empowers participants and clinicians with convenient, accurate electronic outcome reporting for clinical trials, enhancing data quality and study efficiency.
- Medrio Clinical Data Services
Provides tailored clinical data management support to accelerate trials, improve data integrity, and enable internal teams.
- Electronic Data Capture (EDC) Software
Medrio's EDC system streamlines clinical trials with real-time data access, secure management, and efficient study builds.
- Clinical Trial Project Management
Provides expert project management services to streamline clinical trials, enhance data quality, and ensure compliance.
- Randomization and Trial Supply Management (RTSM)
A no-code RTSM solution for clinical trials, offering automated randomization, supply chain optimization, and seamless participant management.