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Medrio

Electronic data capture and clinical trial management for sponsors and CROs, with no-code configuration and integrated ePRO, eConsent, and RTSM.

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Overview

Medrio is a clinical trial technology company offering an electronic data capture (EDC) platform purpose-built for small and scaling life sciences teams, including sponsors and contract research organizations (CROs). Combining enterprise-grade rigor with no-code agility, Medrio delivers a fully validated, audit-ready EDC backed by more than 20 years of clinical use across thousands of completed studies and millions of enrolled subjects. The platform is trusted by industry leaders across 30+ countries and is designed to help resource-conscious teams achieve more without added complexity, hidden costs, or risk.

Unlike traditional EDC platforms that force teams to choose between bloated enterprise systems and lightweight tools that lack scalability or industry expertise, Medrio occupies a distinct middle ground — offering powerful functionality that can be configured, adapted, and managed without requiring programming knowledge. Teams can write simple Excel-style algorithms rather than JavaScript or deep coding, enabling faster, easier access to data and significantly reducing the burden on in-house technical staff.

Core Platform and Solutions

  • EDC/CDMS: A fully validated, audit-ready electronic data capture and clinical data management system designed to support studies from early phase through post-market research.
  • ePRO/eCOA: Electronic patient-reported outcomes and clinical outcome assessment tools integrated directly within the platform.
  • eConsent: Digital informed consent capabilities built into the all-in-one platform.
  • RTSM: Randomization and trial supply management functionality to support complex study logistics.
  • All modules are available within a single, unified platform that scales easily across study phases and therapeutic areas.

No-Code Flexibility and Configuration

  • Sponsors and CROs can configure and manage the platform without a programmer, reducing dependency on technical resources.
  • The no-code environment enables significantly faster mid-study changes, allowing teams to adapt protocols and study designs in real time.
  • Faster database lock times are achieved through real-time data management and built-in data quality controls.
  • Teams can selectively use only the features they need, even for complex studies, without sacrificing quality or service.

Integration Capabilities

  • Devices and eSource: Automatically ingests data from wearables, sensors, and external devices.
  • Labs and LIMS: Imports structured lab results, metabolic panels, and sample data from central, local, or point-of-care laboratories.
  • Analytics and BI Tools: Exports clean, machine-readable clinical and metadata to power dashboards, reporting, and advanced analytics.
  • Data Lakes and Warehouses: Streams complete clinical and study metadata into data lakes or warehouses for long-term analysis and cross-study insights.
  • Robust import and export APIs enable connectivity across the full ecosystem of clinical trial solutions.

Professional Services and Expert Support

  • Clinical Trial Project Management: Medrio provides support from seasoned project managers, data scientists, and product experts to help accelerate timelines and mitigate risk for smoother, smarter trials.
  • Clinical Trial Data Services: A dedicated team of 17 experts with a combined 300 years of industry experience, offering support across database build, data management, biostatistical analysis, and regulatory-ready outputs.
  • eClinical consulting is available from protocol design through database lock, helping teams make informed decisions and avoid common pitfalls.
  • Customer support is consistently available, with Medrio described by clients as establishing a genuine working partnership rather than a transactional vendor relationship.

Deployment and Customer Profile

  • Medrio has deployed studies globally, with sites operating across more than 30 countries.
  • The platform supports thousands of completed clinical trials and millions of enrolled subjects.
  • Medrio maintains a high customer retention rate, reflecting strong satisfaction among sponsors, CROs, and research centers.
  • Customers include organizations such as CTRG, the Digital Medicine Society, MAC Clinical Research, Rose Research Center, and Nevro, among others.

Medrio is designed for life sciences teams that need the power and compliance of an enterprise EDC without the overhead, rigidity, or cost typically associated with large-scale platforms. By combining validated technology, no-code configurability, deep integration capabilities, and hands-on expert services, Medrio enables clinical teams to produce high-quality data, reduce timelines, and scale their research operations efficiently.