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 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...
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.
Webinar
CDMS / EDC•DCT
Navigating Early-Phase Clinical Trials: Key Considerations for Emerging Biotech and MedTech
This webinar explores the essential strategies and solutions for efficiently navigating clinical trial data collection, technology integration, and strategic planning to achieve FDA approval and secure payer reimbursement.