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SCDM 2023

Stay up-to-date with the latest resources, announcements, and news from Medrio.

Solutions and success stories

Medrio CDMS/EDC

Medrio CDMS/EDC

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. 

Medrio eCOA/ePRO

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. 

Medrio eCOA/ePRO
Medrio eConsent

Medrio eConsent

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.

Medrio RTSM

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.

Medrio RTSM
finding-the-right-edc-solution

Finding the Right EDC Solution for Your Next Clinical Trial

Medrio's latest guide, helps you navigate the EDC selection process with ease. Learn how to choose an EDC that fits your research needs by discovering the important factors and features to consider, such as usability, scalability and…

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importance-quality-data-meeting-fda-regulatory-scrutiny

Importance of Quality Data in Meeting Increasing FDA Regulatory Scrutiny

Partnering with a reliable EDC vendor to ensure your clinical trial data meets high standards of accuracy and integrity is essential for passing FDA scrutiny. Risk-based approaches and...

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hmr-statistics-data-management-group

HMR’s Statistics & Data Management Group Reaches New Heights of Clinical Trial Efficiency With Medrio EDC

Medrio EDC has boosted HMR's Statistics & Data Management group...

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fully-remote-hybrid-flexible

Fully Remote, Hybrid, or Flexible Hybrid Decentralized Trials

CROs and sponsors must consider multiple factors when deciding between a fully remote, hybrid or flexible hybrid approach for their clinical trial. Read up on the key considerations here!

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want-to-boost-retention-drive-trial-success

Want to Boost Retention and Drive Trial Success? You Need Participant Comprehension, Not Consent

eConsent is transforming the informed consent process, making it easier for…

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Success Story: 3 Steps To Success: How Swing Therapeutics Harnessed Medrio Solutions to Secure FDA Clearance

3 Steps To Success: How Swing Therapeutics Harnessed Medrio Solutions to Secure FDA Clearance

Discover how Medrio CDMS/EDC, eCOA/ePRO, and eConsent supported Swing Therapeutics in securing FDA clearance.

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