The primary pain point is manual inefficiency. Clinical research coordinators spend up to 30% of their time manually screening patient records against dense, complex eligibility criteria. This leads to slow enrollment, high screen-out rates, and missed opportunities to match eligible patients. The result is extended trial timelines, costing sponsors millions per day in delayed revenue and delaying patient access to novel therapies. This manual process also inherently limits trial diversity, as it cannot efficiently scan broad, heterogeneous patient populations.













