Powering your research potential.
Trusted by the world’s top clinical trial sponsors and CROs
From protocol design to casebook submission, we’re with you every step of the way.
Improve Data Flow
Our solutions are integrated via one unified experience, so you can easily monitor progress, understand trends, and generate meaningful insights.
Optimize Workflows
Configure and adjust workflows to meet the needs of sites and participants — without compromising speed, quality, or control.
Increase Engagement
From consent to database lock, Medrio enables you to engage with participants and capture quality data from anywhere – at any time.
Improve Data Flow
Our solutions are integrated via one unified experience, so you can easily monitor progress, understand trends and generate meaningful insights.
Optimize Workflows
Configure and adjust workflows to meet the needs of sites and participants – without compromising speed, quality or control.
Increase Engagement
From consent to database lock, Medrio enables you to engage with participants and capture quality data from anywhere – at any time.
Our Approach
We’re just the right size to deliver personalized support and experienced enough to provide the global reach, expertise, and resources you need. With almost two decades leading the industry, we understand your unique challenges and can meet you wherever you are on your journey – guiding you toward success at an accelerated pace.
Our Solutions
Engineered to handle complexity without compromising ease-of-use, Medrio allows you to concentrate on the science – not the technology. Our solutions are designed for ease of use, and are scalable and connected through one unified platform, providing real-time access and control of your trial data so you can take your trial farther, faster.
More than just an electronic data collection (EDC) tool, Medrio’s clinical data management system (CDMS) combines an intuitive user interface, seamless on and offline data capture capabilities, and comprehensive data management in a single solution.
With a user-friendly interface and flexible data capture options, Medrio’s electronic clinical outcome assessment (eCOA) and electronic patient-reported outcome (ePRO) solution empowers participants, clinicians, and observers to conveniently and accurately report outcomes, enhancing data quality and study efficiency.
Ensure compliance, increase comprehension, and empower efficient study management with Medrio eConsent. Robust features like multi-signer support and paper consent uploads enable participants to consent from anywhere – remotely or onsite.
Effectively randomize, manage, and control your trial supplies and minimize risks with our robust randomization and trial supply management (RTSM) solution. Advanced features enable you to configure allocation rules, automate shipment approvals, and receive issue notifications to streamline the supply chain process.
Our Promise
At Medrio, we’re devoted to providing our customers with the autonomy they deserve and the freedom to make decisions with confidence. Our expertise, enablement services and high-touch support ecosystem ensure lightning-fast responsiveness and flexibility so you can move fast – from the start.
