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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Success Story
CDMS / EDC

Ancillarie Experiences Efficient Study Build with Medrio

It’s not often that two clinical data managers who are years apart in their experience feel equally at ease during a clinical trial. But this is precisely what took place...

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MarketExpertise AnimalHealth 1024x1024 1
Success Story
CDMS / EDC

Clindata Gains Efficiency for Animal Health with Medrio EDC

Clindata International, a South Africa-based CRO specializing in Animal Health clinical trials, has used Medrio EDC since 2013.

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epro happy user
Success Story
DCTeCOA / ePRO

Swing Therapeutics Achieved 97% Patient Compliance with ePRO

Swing Therapeutics leveraged Medrio ePRO in a proof-of-concept for a decentralized hybrid study. Electronic Patient-Reported Outcomes (ePRO) technology was used to assess the results of varying digital therapies and the...

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Success Story
CDMS / EDC

The Right EDC Gives Paragonix Technologies Ultimate Autonomy with a Lean Team

Paragonix Technologies selected Medrio EDC for their GUARDIAN-HEART clinical study. Electronic Data Capture (EDC) technology is being used to collect and manage registry data, examining the effect of controlled hypothermic...

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oncology patient hope
Success Story
DCTeConsent

TargetCancer Foundation Successfully Engages and Empowers Rare Cancer Patients with Medrio

TargetCancer Foundation implemented Medrio’s remote consent function in their TCF-001 TRACK study, which has an objective to determine if rare tumors can benefit from matched molecular therapy. The study is...

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Patient Engagement Guide for Sponsors and CROs 2021 1
White Paper
CDMS / EDCeCOA / ePROeConsenteSource

Patient Engagement Guide for Sponsors and CROs

Now, more than ever, sponsors and CROs need to prioritize including patient engagement in their study builds from the ground-up. This involves defining processes to remove barriers for access, increasing awareness and education for clinical trials, and creating effective exchanges between patients and their clinicians.