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.
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...
Blog
CDMS / EDC•eCOA / ePRO•eConsent•RTSM
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.
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.
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.
Success Story
CDMS / EDC
How Visby Leveraged Medrio CDMS/EDC for FDA De Novo Authorization
Visby used Medrio CDMS/EDC for clinical study data management and to gain FDA De Novo authorization. Learn how their data strategy drove success.
eBook
eCOA / ePRO•eConsent
eCOA & eConsent Planning Workbook
Use this interactive workbook to ensure you have the right information to evaluate eCOA and eConsent effectively.