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
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
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.
Webinar
eCOA / ePRO•eConsent
Designing ePRO and eConsent Solutions that Participants and Sites Want
In this webinar, we will explore the powerful way that ePRO and eConsent tools, when implemented effectively, can enhance the participant experience and improve compliance while reducing the burden on site staff.
eBook
eCOA / ePRO
Facts and Misconceptions about ePRO Cost-Effectiveness
Gain guidance on misconceptions around the cost-effectiveness of electronic patient-reported outcomes (ePRO) and key points to consider when evaluating ePRO.
Success Story
CDMS / EDC•eCOA / ePRO
OncoBay Relies on Medrio ePRO and EDC for Easier, Cleaner Data
Collecting participant data securely is a critical part of running any clinical trial, whether it is decentralized, in-clinic, or somewhere in between. Medrio EDC and ePRO solutions are important assets that help CROs and sponsors do more with less.