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.
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.
Podcast, Blog
Digital Behavioral Therapy for Fibromyalgia
July 23, 2025
Learn about the process of running digital therapeutic trials to receive FDA De Novo marketing authorization.
Blog
RTSM
IRT in Clinical Trials: A Practical Guide for Supply Chain and Clinical Ops
July 16, 2025
Read this blog to learn IRT definitions, benefits, primary functions, and more.