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
DCT•eSource
3 Reasons Why eSource Is a Must for Global Trials
July 10, 2019
What Is eSource? Source data is the initial data recording, and eSource is any source data that is recorded electronically with the goal of producing the highest quality data— faster. ...
Blog
CDMS / EDC
Adaptive Trials: Is Your Study Equipped To Adapt?
May 20, 2019
Imagine, for a moment, you’re a data manager overseeing a Phase I study. Your endpoints are set, your database built and deployed, and your data collected. Now it’s time to...
Blog
CDMS / EDC
Avoiding Headaches In Today’s Complex Phase I Landscape
May 16, 2019
Statistics suggest that Phase I clinical trials, while by no means free of challenges, are more manageable than later phases. They tend to take less time and cost less money;...
Blog
Data Quality in Your eClinical System — What’s at Stake for a CRO?
September 15, 2018
If you know Medrio — if you’ve interacted with us at industry conferences, perused our site, or spend a good amount of time on this blog — you know that...
Blog
70 Clinical Trial Abbreviations and Acronyms (Quick Guide)
August 3, 2018
When we talk to people who are new to our industry, one of the toughest things for them to wrap their heads around is the clinical trial abbreviations and acronyms...
Blog
CDMS / EDC
3 Early Obstacles in Phase I Clinical Trials, And How to Address Them
April 15, 2018
Anyone with an involvement or interest in clinical research is likely to be aware of the challenges in clinical trials, and in getting their compounds approved by the FDA. The...