March 4, 9:00am PT
Advancing clinical trials with real-world data
Smarter designs, faster recruitment, and ongoing follow-up
Clinical trials are increasingly constrained by slow recruitment, protocol amendments, and limited visibility into real-world care. As sponsors seek faster, more inclusive, and more efficient trials, real-world data is becoming an essential need-to-have for successful study design and execution.
In this webinar, learn how Truveta Data—daily refreshed, longitudinal EHR data linked with claims and social drivers of health—supports a new approach to clinical development.
We will explore how life sciences researchers are using Truveta to:
- Reduce trial risk and complexity with dynamic cohort design and instant feasibility modeling.
- Accelerate site selection and patient enrollment with precision using complete, real-time clinical data.
- Extend evidence generation beyond the trial period with longitudinal follow-up for safety, adherence, and outcomes.
Join us to see how regulatory-grade real-world data can help sponsors move faster—from trial planning through post-study evidence generation—without compromising rigor or representativeness.