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
European Medical Device Regulation: 5 Steps to Prepare for What’s Coming
Discover how the EU MDR is already impacting companies and learn what you can do to prepare for its full release.
Success Story
CDMS / EDC•eCOA / ePRO•eConsent
3 Steps To Success: How Swing Therapeutics Harnessed Medrio Solutions to Secure FDA Clearance
Discover how Medrio CDMS/EDC, eCOA/ePRO, and eConsent supported Swing Therapeutics in securing FDA clearance.
eBook
CDMS / EDC•eCOA / ePRO•eConsent•RTSM
Opportunities in Rare Disease Research: Embracing Unique Considerations
Discover insights from leading experts and learn strategies specific to rare disease research for engaging patient communities, retaining participants, designing studies, and optimizing supply chain.
Blog
How Data Is Reshaping the Future of Clinical Trials
September 1, 2023
Data management in clinical research is at an inflection point. Learn what you can do to create more accurate, high-quality clinical trials.
Blog
CDMS / EDC•eCOA / ePRO•eConsent
The Moral Obligation: Digital Data Capture for Patient-Centric Trials
August 4, 2023
Digital data capture, such as electronic data capture (EDC), ePRO, and eConsent, create patient centricity and enable accurate data collection.
eBook
CDMS / EDC
Finding the Right EDC Solution for Your Next Clinical Trial
Medrio's latest guide, helps you navigate the EDC selection process with ease.Learn how to choose an EDC that fits your research needs by discovering the important factors and features to consider, such as usability, scalability and security.