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
CDMS / EDC
Fast-Track Your Database Lock: 8 Best Practices for Smoother Study Closeout
In this eBook, learn expert strategies for faster database lock and study closeout.
Blog
CDMS / EDC
Artificial Intelligence in Clinical Trials: The Current State of Global Regulatory Frameworks
November 6, 2024
In this blog, understand the current state of published regulatory frameworks for AI in clinical trials.
Infographic
CDMS / EDC
12 Questions to Consider for Using AI in Clinical Trials
In this infographic, see at-a-glance what you should consider when exploring the use of AI in clinical trials.
eBook
CDMS / EDC•eCOA / ePRO•eConsent
A Medical Device Sponsor’s Guidebook: How to Navigate Clinical Trials
Navigating medical device clinical trials? Learn best practices for better clinical trial operations and data management.
Blog
CDMS / EDC
Preparing for the CTIS: How the EU CTR Impacts Clinical Trials
October 8, 2024
In this blog, learn actionable tips to prepare for the Clinical Trials Information System (CTIS) under the EU CTR.
eBook
The CRO’s Playbook for Better Trial Operations & Sponsor Partnerships
In this eBook, CRO’s can learn how to build resilient partnerships, support complex studies, and capture a new pipeline of R&D work.