ClinOne Supports Clinical Research Organizations (CROs) with Enterprise eConsent to Add Immediate Value for Customers, Accelerate Timelines, and Maintain Study Budgets

▤ Summary

ClinOne solves these issues with an easily configurable and interoperable platform that makes it cost effective for mid-size and emerging CROs to provide reliable eConsent for customers at any scale. To learn more about eConsent, ClinOne invites CROs of all sizes to join an educational 30-minute webinar to showcase the value it adds for patients, sites, and study teams – and features to look for when evaluating a technology partner. Webinar: eConsent for CROs: Improve Your Win Rates Without Breaking Your Budget Date and Time: May 26, 10-10:30am ET Presenters: Rob Bohacs (CEO and Co-Founder, ClinOne) and Mindy Gruba (Senior Director, Product) Registration: Register here The webinar will cover topics such as… • Proven benefits of eConsent for CROs – and why demand is soaring • How to select the best technology feature The webinar also will include a live solution demonstration, which will showcase key features: • Integrated consent and video meetings with up to 10 participants “eConsent is everywhere – and for good reason,” said Kristopher Sarajian (LinkedIn), VP of Marketing at ClinOne, who will moderate the session. As the CEO of an oncology CRO and site management organization, Rob unified 320 oncology research centers across the U.S. Mindy Gruba, Senior Director, Product, ClinOne – Mindy manages the ClinOne product roadmap by synthesizing technology development with customer requirements and real-world feedback from global site and patient platform members. Featuring proven global logistics, the industrys fastest implementation timelines, and an all-star team of senior executives, technologists and service professionals, ClinOne makes clinical research a little easier, every day, for patients and sites worldwide.

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ClinOne

$1M to $5M