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.

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database person on computer
Blog
CDMS / EDC

5 Ways To Prevent Costly Database Delays

April 17, 2023
Delays in a clinical trial process can have serious downstream consequences, such as missing a go-to-market window or preventing life-changing solutions from reaching the people who need them as soon as possible. Here are five tips to reduce the risk of database delays.
rtsm tablet user 1
Infographic
RTSM

5 Ways RTSM Supports Study Managers

Discover the benefits of using Randomization and Trial Supply Management (RTSM) systems for study managers in this infographic.
eclinical tech blog
Blog
eCOA / ePROeConsent

Patient-Centricity Is in Everything We Do: Designing Accessible eClinical Technology

April 11, 2023
Medrio is dedicated to making the clinical trial journey easier by creating thoughtful UX designs that emphasize what’s most important and lead to better participant outcomes. Discover how Medrio provides users with streamlined technology solutions for their clinical trials, as well as tips on improving the participant experience.
AdobeStock 378541028
Blog
eCOA / ePRO

ePRO for Early Phase Studies: 3 Ways To Benefit

March 20, 2023
Adopting ePRO in early-phase trials can revolutionize data collection, reduce participant burden and increase the accuracy of results. Not only does this improve patient care, but it also provides commercial advantages to sponsors.
Closeup of female texting on her cellphone
Success Story
CDMS / EDCeCOA / ePRO

NeuraLace Doubles Clinical Trial Enrollment and Improves Participant Compliance with Medrio’s EDC and ePRO

Emerging medical device company NeuraLace doubles clinical trial enrollment and demonstrates improved participant compliance with Medrio’s EDC and ePRO offerings.
epro header blog bg
Blog
eCOA / ePRO

3 Steps To Improve Site Acceptance of ePRO in Medical Device Trials

March 1, 2023
Medical device organizations aim to reduce development time by 25% in the next five years. The adoption of ePRO can help make this goal a reality.

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