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.
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."
Blog
eCOA / ePRO
How to Overcome the Problem of the Early ePRO Oversell
November 8, 2022
With increasing regulatory requirements for the inclusion of patient-reported outcomes in study data, maintaining the status quo in PRO collection can have costly consequences.