Resource Library

Meridians look back on 20 years of teamwork, innovation, and supporting research through eClinical technology.

Learn how Visby achieved FDA De Novo authorization using Medrio CDMS/EDC – submitting their application just 45 days after the final participant's visit.

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.