Lower the Cost & Eliminate Barriers to Launching Studies
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).
Modern Registries
Prospective Studies
Randomized Trials
Multicenter Studies
Real-World Evidence
Market Surveillance
Electronic Data Capture (EDC)
Pull Together Data Across the Entire Evidence Spectrum
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.
E-Consent
Accelerate All Phases of the Consenting Process
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.