Trusted by sponsors, CROs, and sites worldwide, Medrio aims to improve 100 million lives through faster, more efficient, and secure clinical trials. With almost two decades of experience, Medrio delivers proven, scalable solutions, unrivaled customer support, and guidance to the industry’s leading innovators, including pharmaceutical, biotech, medical device, diagnostics, and more. 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. Experience the power of Medrio and realize the full potential of your clinical operations and outcomes.


FEATURED CONTENT

More than just an electronic data collection (EDC) tool, Medrio’s clinical data management system (CDMS) combines an intuitive user interface and comprehensive data management in a single solution to give you full control over your study data.

Our drag-and-drop builds and automated workflows introduce new efficiencies without compromising data quality. When your data capture strategy is built on the right technology foundation, anything is possible – including shorter timelines that allow you to scale up with ease.

Complete study builds in less than 3 weeks, compared to the industry average of 12 weeks

  • Make mid-study changes in as little as a day with no downtime
  • Build your own library of reusable study templates
  • Maintain real-time visibility into trial data

Medrio CDMS/EDC scales with you as you grow. No matter the study size or phase, our technology safeguards your most important asset: your data.

Learn more: https://medrio.com/electronic-data-capture-edc/

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