[August '23] Resource Roundup

[August '23] Resource Roundup

Welcome to our monthly Resource Roundup edition of Trial Talks with Medrio, where we share hand-selected insights from the top minds in clinical trials.?

Each month we explore engaging topics like the latest clinical technology trends, upcoming research regulations, and much more! To get more insights like these straight to your inbox, subscribe to our email list.


Does the 10,000-Hours Rule Apply to Clinical Trials?

When engaging CROs, sponsors are increasingly prioritizing performance excellence and replicable operating standards.

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Notes from the Field: How eConsent Improves Clinical Trials

Employing eConsent benefits participants, sites, sponsors and CROs. In this article, a Medrio Subject Matter Expert explains how this technology creates important advantages for all clinical trial stakeholders.

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HMR’s Statistics & Data Management Group Reaches New Heights of Clinical Trial Efficiency With Medrio EDC

Medrio EDC has boosted HMR's Statistics & Data Management group with an intuitive build functionality, automated query firing, and skip logic, increasing efficiency and accuracy. This scalable solution offers cost-effective data quality and exceptional service levels for sponsors, making the transition from paper-based processes seamless.

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