Expanding the Role of External Control Arms: A Strategic Approach to Modern Clinical Research

External control arms (ECAs) are transforming clinical trials by enhancing efficiency, reducing costs, and addressing ethical challenges. By leveraging real-world data (RWD), ECAs can supplement or replace traditional control groups—accelerating the availability of life-changing therapies, particularly in high-need indications.
This white paper explores the growing role of ECAs in clinical research and how Verana Health’s curated, research-ready datasets are driving regulatory-grade real-world evidence (RWE) generation.
Access a copy of the white paper to learn:
- The Role of ECAs in Rare and Complex Diseases – How ECAs help overcome recruitment challenges and provide meaningful comparative evidence.
- Regulatory Trends and ECA Best Practices – Insights into FDA guidance and the critical factors needed to ensure scientific rigor.
- Verana Health’s Cutting-Edge Approach – How high-quality RWD and AI-powered Qdata® accelerate study timelines and enhance clinical trial diversity.
Download the white paper to discover how ECAs are shaping the future of clinical research.
• How rgulatory-grade data is being used in ophthalmologyRequest a Copy
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