Easily build and enroll patients into research studies designed around specified outcomes for a population defined by a particular disease, condition, or exposure, which serves a predetermined scientific, clinical, or policy purpose(s).
Harness the power of collecting, storing and analyzing de-identified, real-world data from a variety of sources, including directly from patient chart with electronic health record (EHR) integrations, to increase data visibility and inform decision-making across the value chain.
From building and modifying forms, to ensuring patient comprehension and compliance, our platform streamlines and automates study enrollment, screening, and consent with customizable workflows that are fully compliant with US 21 CFR Part 11 electronic signature requirements.
The fastest growing network for collaborating on clinical research and improving patient outcomes.