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/
CONTACT INFORMATION
Medrio
345 California Street, Suite 325
San Francisco, CA 94104
UNITED STATES
Phone: +1 415-963-3700
Contact: Denise Spillane
SOLUTION SHEETS
EDC
EPRO
RTSM
ECONSENT
CUSTOMER STORIES
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Uncover how this CRO was able to stay agile by choosing a CDMS/EDC partner that prioritized sponsor needs and streamlined operations to achieve top-tier results swiftly.
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Discover how a partnership with one of Europe’s largest contract research organizations exemplifies the crucial role that technology plays in the realm of clinical studies.
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Delve into the five key ways this biotech company was able to successfully deliver data quality and compliance for large-scale trials while developing next-generation blood tests for early cancer detection.
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Dive into how a suite of solutions enabled a decentralized approach, relieving site burdens, advocating data, and demonstrating safety and efficacy to regulatory authorities.
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Find out how one company dedicated to producing innovative non-invasive chronic pain therapies was able to engage its patients in new ways.
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Find out why one leading biotechnology company keeps choosing this eClinical technologies and services provider for EDC assistance.
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Read how a global medical device company was able to unlock new efficiencies by implementing data collection via electronic patient-reported outcome assessments.
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Learn how a therapeutic oncology company was able to take advantage of an EDC system, establish a ePRO assessments collections platform, and receive guidance on data collection devices.
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After experiencing paper processing issues, discover how a company transitioned to digital data collection by using Electronic Data Capture (EDC) and Electronic Patient Reported Outcomes (ePRO) solutions.
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By using Medrio’s EDC platform, learn how Atlantic Research Group was able to achieve the flexibility needed to span multiple therapeutic areas and eliminate redundancy in documentation.