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.
Blog
CDMS / EDC•eCOA / ePRO•eConsent
The Moral Obligation: Digital Data Capture for Patient-Centric Trials
August 4, 2023
Digital data capture, such as electronic data capture (EDC), ePRO, and eConsent, create patient centricity and enable accurate data collection.
eBook
CDMS / EDC
Finding the Right EDC Solution for Your Next Clinical Trial
Medrio's latest guide, helps you navigate the EDC selection process with ease.Learn how to choose an EDC that fits your research needs by discovering the important factors and features to consider, such as usability, scalability and security.
Blog
eSource
Why eSource Ensures Data Integrity in Medical Device Clinical Trials
July 14, 2023
Understand the challenges with source data verification and learn how eSource affects clinical trials and improves data integrity.
Webinar
Moving Beyond Tech Adoption: The Future of Clinical Trial Technology
Join the insightful webinar on the evolution of clinical technology, growing complexity of clinical research and uncover the current challenges and gaps in eClinical tech. Our esteemed speakers, including Medrio's CEO Nicole Latimer, will share their expertise and discuss the future of trials.
eBook
DCT
Fully Remote, Hybrid, or Flexible Hybrid Decentralized Trials
CROs and sponsors must consider multiple factors when deciding between a fully remote, hybrid or flexible hybrid approach for their clinical trial. Read up on the key considerations here!
White Paper
eCOA / ePRO
Utilization of Patient-Reported Outcomes for Medical Device Trials
Medical device sponsors are diversifying study formats, using ePRO tools like apps and web-based solutions. A survey by Medrio and studioID shows that over 90% find ePRO valuable for device trials.