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.
Blog
CDMS / EDC
How to Navigate Data Complexity with Medrio’s AI-Enabled Reporting
April 18, 2025
In this blog, learn how Medrio’s AI-enabled reporting will help you better understand your clinical trial data.
Blog
CDMS / EDC•eCOA / ePRO•eConsent
Clinical Trials Medical Device Guidelines: What Sponsors Should Know
March 26, 2025
Curious about medical device clinical trials? Learn tips on regulations, trial design, technology, and more!
Blog
CDMS / EDC
Database Lock in Clinical Trials: How to Make the Process Easier and Faster
March 3, 2025
In this blog, learn field-tested tips on how to get to database lock (DBL) in clinical trials as quickly as possible.
Blog
CDMS / EDC
How the EU AI Act Affects Clinical Trials
February 24, 2025
In this blog, explore how the EU AI Act impacts clinical trials, from risk classification to compliance strategies.
Blog
CDMS / EDC•DCT•eCOA / ePRO•eConsent
What is eSource in Clinical Trials
February 3, 2025
In this blog, discover what eSource is, how it works, and why it benefits clinical trials.
Blog
CDMS / EDC•DCT•eCOA / ePRO•eConsent•RTSM
How AI in Clinical Trials Shapes the Future
January 13, 2025
In this blog, discover how AI is rippling through every segment of clinical trials and how to navigate the new landscape.