The True Science Behind eCOA, Shaped By Patient And Site Insights

Clinical trials sit at a unique intersection of science, patients, and clinical care, and for decades, the “gold standard” has prioritized the rigor of the data, often at the expense of the patients providing it. This gap between rigid protocol requirements and the realities of patients' lives is a primary driver of participant hesitancy and high dropout rates. In eCOA, where patient and site contributions are foundational to data quality, this tension is especially consequential. Visit frequency, required tasks, and device flexibility all shape patient burden, and these on-the-ground realities are too often absent from protocol design.

This webinar brings together patients, sites, and eCOA science to dismantle the researcher-subject hierarchy and replace it with a collaborative model. Through a panel discussion, we’ll translate these perspectives into practical, real-world insights to guide decisions within your protocol. This session aims to offer a more grounded blueprint for scientifically sound protocol design, one where patient and site insights are embedded in the DNA of your eCOA strategy.