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.
Case Study
CDMS / EDC
How Visby Achieved De Novo Marketing Authorization with Medrio CDMS/EDC
Visby used Medrio CDMS/EDC for clinical study data management and to gain FDA De Novo authorization. Learn how their data strategy drove success.
eBook
CDMS / EDC
How to Maximize the Value of CDMS Reporting
In this eBook, you’ll learn why a CDMS with robust reporting capabilities is so important, and what features you can use to reduce uncertainty and make better decisions.
Success Story
CDMS / EDC
How Visby Leveraged Medrio CDMS/EDC for FDA De Novo Authorization
Visby used Medrio CDMS/EDC for clinical study data management and to gain FDA De Novo authorization. Learn how their data strategy drove success.
eBook
eCOA / ePRO•eConsent
eCOA & eConsent Planning Workbook
Use this interactive workbook to ensure you have the right information to evaluate eCOA and eConsent effectively.
Blog
CDMS / EDC
ICH E6(R3) Explained: Insights for European Clinical Trials
August 5, 2025
Understand how ICH E6(R3) is defined, timelines, and ways to prepare.
Blog
CDMS / EDC•eCOA / ePRO•eConsent•RTSM
How to Navigate FDA De Novo Clinical Trials
July 30, 2025
Read this blog to understand the De Novo pathway for medical devices, including best practices, design tips, and more.