The US Food and Drug Administration (FDA) recently published a comprehensive overview of how real-world evidence (RWE) has contributed to regulatory decision-making since 2011. The new webpage, built by the Center for Drug Evaluation and Research (CDER) and the Center...
Medical device manufacturers and regulators face a persistent challenge: obtaining a complete, clinically rich view of how devices are used, how safe they are, and how they affect patient outcomes. Historically, researchers have been limited to claims, chargemaster,...
Today marks the 5 year anniversary of Truveta. I personally am so humbled by where we are today. As I reflect back to where we were in 2020, the world was a very different place. It was a time of great uncertainty. The world was desperate for answers to a pandemic...
At Johns Hopkins University, the Hopkins Business of Health Initiative (HBHI) has launched the HBHI–Truveta User Community, dedicated to fostering a collaborative group of researchers who use Truveta Data to drive cutting-edge research in health and healthcare. Led by...
