Resource Library

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.

Visby used Medrio CDMS/EDC for clinical study data management and to gain FDA De Novo authorization. Learn how their data strategy drove success.

Use this interactive workbook to ensure you have the right information to evaluate eCOA and eConsent effectively.

Understand how ICH E6(R3) is defined, timelines, and ways to prepare.

Read this blog to understand the De Novo pathway for medical devices, including best practices, design tips, and more.

Learn about the process of running digital therapeutic trials to receive FDA De Novo marketing authorization.