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
Is Your CRO’s 2023 Growth Limited by These Four Myths?
January 20, 2023
CROs face growing pressure to differentiate themselves. Myths about sponsor expectations and priorities surrounding eClinical technology can cause CROs to lose bids.
Webinar
eCOA / ePRO
Proven Practices for ePRO Adoption
In this webinar Nicole Latimer and Melissa Newara are joined by Dr. Frances Rubenstein from Nevro to discuss how Nevro, a medical device company, implemented ePRO to close gaps in data accuracy, reduce context switching for staff, and enhance patient convenience.
Success Story
CDMS / EDC
Heron Therapeutics Speeds Up Database Creation with Medrio EDC
San Diego-based biotech trusts Medrio EDC for data collection. From drag-and-drop features to outstanding support, Medrio offers simplicity without compromise.
Blog
CDMS / EDC
Does the 10,000-Hours Rule Apply to Clinical Trials?
November 16, 2022
When engaging CROs, sponsors are increasingly prioritizing performance excellence and replicable operating standards.
Blog
RTSM
When Protocol Amendments Meet RTSM – From Headache to High-Performance
November 10, 2022
Protocol amendments are inevitable, but choosing the right RTSM partner can help you navigate study changes with speed and agility.
Blog
eCOA / ePRO
Medrio’s ePRO Accreditation eLearning Takes Silver in Davey Awards
Medrio, a global leader in eClinical software and services used in decentralized, hybrid, and traditional clinical trials, is pleased to announce it received a Silver Award at the 2022 Davey Awards for its "Build It Better: ePRO Accreditation Program."