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
AI in Clinical Trials: Simplifying the Path to Insights
Clinical trials are becoming increasingly complex, with a growing volume of data, forms, and regulations to manage. How can sponsors and CROs navigate this rising complexity while maintaining speed, quality,...
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.
Infographic
CDMS / EDC
UAT in Clinical Trials Guide
In this infographic, learn best practices for navigating user acceptance testing (UAT) for smoother, more efficient database builds.
News
Medrio Launches AI-Enabled Reporting, Tackling Increasing Data Challenges in Clinical Trials
SAN FRANCISCO, CA – January 29, 2025—Medrio, a global leader in clinical trial technology, today announced the release of AI-enabled reporting, an innovative new capability available within Medrio CDMS/EDC. Medrio’s...