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Hosted Session/Non-CE: Case Study hosted by Truveta: Accelerating Evidence Generation: Delivering Insights Ahead of Trials and Registries
Session Chair(s)
Sponsored Sessions
United States
Traditional clinical trials and registries take years to generate post-market evidence, leaving critical knowledge gaps that delay patient and provider decision-making. Using Truveta Data – which includes complete EHR data linked with claims and genomic information – researchers have rapidly generated high-quality real-world evidence well ahead of traditional methods. This presentation will highlight two case studies: (1) a GLP-1 comparative effectiveness study that produced results over a year before a major trial, later validated by trial findings, and (2) a device manufacturer that replicated registry outcomes with a significantly larger, more contemporary patient cohort. These examples showcase how real-world data can deliver timely, scalable, and clinically meaningful insights.
Learning Objective : - How Truveta Data delivers real-world evidence faster than trials and registries, enabling earlier, data-driven decisions
- How linked EHR, claims, and genomic data can be used to power comprehensive, high-quality pre- and post-market research
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How Truveta Data meets and exceeds FDA standards, supporting regulatory submissions of audit-ready real-world evidence
Speaker(s)
Exhibitor
Conor Wyand
Truveta, United States
Vice President of Partner Growth
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