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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Webinar
RTSM

5 Supply Management Success Factors for Your Early Phase Studies

Many early phase studies rely on manual methods of managing participant randomization and the study supply chain. But increasing complexities in both study design and global supply chain necessitate more flexible, responsive solutions for early phase studies, in particular. 
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Blog
RTSM

How Are You Labeling Your IP? Protect Your Clinical Trial with Distinct Treatment Numbers

September 6, 2022
Does your CRO or sponsor have a policy around IP numbering in clinical trials? If not, they could be putting your clinical trial at risk.
Blog

Medrio Completes Successful Type 2 System and Organization Controls (SOC) 2 Examination

September 1, 2022
San Francisco, CA (August 19, 2022) — Medrio, a global leader in eClinical software and services used in decentralized, hybrid, and traditional clinical trials, has successfully completed a System and Organization Controls (SOC) 2 Type 2 examination. The independent third-party report attests to the controls at Medrio regarding the security, availability, and confidentiality of its eClinical technology and solutions.
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Blog
RTSM

Winning the Race to FPI with Early Randomization and Trial Supply Management

August 25, 2022
Smart IP Packaging Helps Clinical Trials Avoid Supply Chain Hurdles to Study Startup Ian Davison, Ph.D. Neuroscience, Medrio’s In-house RTSM Subject Matter Expert Packaging decisions may seem benign, but they...
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Success Story
eConsent

Digital Medicine Society Accelerates Recruitment and Results with Medrio’s eConsent

The Digital Medicine Society (DiMe), an interdisciplinary professional society for digital medicine, was able to deploy Medrio’s eConsent module in less than two weeks to support its remote study to...
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Podcast

Achieving Patient Centricity by Removing Barriers in the Clinical Trial 

In this episode, we discuss with Kafayat Babajide, Director of Patient Insights & Experience with Johnson and Johnson, the ways in which a patient-centric approach can remove controllable barriers from the clinical trial process.