Resource Library

We’ve compiled a useful collection of resources to learn more about Medrio and various aspects of managing your clinical trial in today’s complex and evolving environment.

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eBook
CDMS / EDC

Where EDC Can Make or Break Your Timeline

This guide highlights how Medrio’s CDMS/EDC and experienced team can support your trial throughout its entire lifecycle.
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White Paper
CDMS / EDCeConsent

Canada’s Rising Role in Global Clinical Trials

This guide explores the current state of clinical trials in Canada and what’s driving interest from global sponsors.
Webinar Start Strong Strategies for Early Phase Trial Success
Webinar
CDMS / EDC

Start Strong: Strategies for Early Phase Trial Success

Are you navigating tight timelines, limited funding or high expectations? For early phase sponsors, trial planning is full of risk—and misalignment between Clinical Operations and Data Management is one of...
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Blog
CDMS / EDCeCOA / ePROeConsentRTSM

Twenty Years of Teamwork: Top Medrio Moments

September 22, 2025
Meridians look back on 20 years of teamwork, innovation, and supporting research through eClinical technology.
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Case Study
CDMS / EDC

How Visby Achieved De Novo Marketing Authorization with Medrio CDMS/EDC

Learn how Visby achieved FDA De Novo authorization using Medrio CDMS/EDC – submitting their application just 45 days after the final participant's visit.
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eBook
CDMS / EDC

How to Maximize the Value of CDMS Reporting

In this eBook, you’ll learn why a CDMS with robust reporting capabilities is so important, and what features you can use to reduce uncertainty and make better decisions.