Sponsored by Truveta
Traditional clinical trials are slow and costly, often hindered by delays, amendments, and recruitment challenges. As sponsors face mounting pressure to conduct faster, more inclusive studies, real-world data (RWD) is transforming how trials are designed and executed.
Truveta Data has been used to replace costly registries, emulate external control arms, support label expansion, and generate regulatory-grade evidence recognized by agencies such as the FDA and CMS—all while reducing time, cost, and complexity.
In this webinar, you’ll learn how leading life sciences organizations are modernizing clinical trials with complete, daily updated, and trusted RWD directly from US health systems.
With de-identified, longitudinal EHR data representing more than 120 million patients, Truveta Data enables sponsors to identify optimal sites and participants faster, design more inclusive and efficient studies, and prospectively track patient outcomes far beyond the traditional trial window. Participants will gain a clear view of how real-world data can improve feasibility modeling, accelerate recruitment, and enable longitudinal follow-up for safety, adherence, and outcomes research.
By the end of this session, participants will understand:
• How access to complete, real-time, regulatory-grade data from Truveta enables faster recruitment, site selection, and trial execution.
• How leading sponsors are using Truveta Data to design more efficient, inclusive studies—using dynamic feasibility modeling and real-world comparators to de-risk protocols, emulate external control arms, and support regulatory submissions and label expansion
• How longitudinal linkage across EHR, claims, and registry data extends trial impact through long-term follow-up, safety monitoring, and outcomes research.
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