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.
eBook
CDMS / EDC
How to Run a Nimble, Cost-Effective Clinical Trial in Any Industry Climate
Volatility is constant in clinical trials. Learn how to run a nimble, cost-effective clinical trial in any industry climate.
eBook
CDMS / EDC
How to Protect Data Quality in Clinical Trials
Bad clinical trial data can threaten market approval. Learn how to protect your data and meet standards for accuracy, consistency, and reliability.
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.