top U.S. research institutions use our platform
eCRF and CLINRO completeness
improved productivity for site workflows
Flexible solutions that scale with you
Meet changing study needs without cumbersome implementations or the addition of new technology vendors.
Rapidly set up your study
Launch siteless or hybrid studies in weeks with customizable workflows, cutting costs by 30 to 50% and avoiding vendor overages.
Integrate complex data capture
Capture complex, multimodal data from sites, patients, labs, and 60,000+ care centers, unified and audit‑ready from day one to enrich your registry.
Leverage analytics & bioinformatics
Normalize, enrich, and analyze data with our AI-powered platform designed for complex modalities and longitudinal datasets.
Recruit engaged patients
Stay connected with our vibrant patient communities to gather ongoing, fully consented follow‑up insights—enabling future research opportunities.
How it works
Real-world data from 60,000+ care centers
All data modalities: eCRFs, CLINROs, biospecimens, raw molecular, imaging, spectral, ePROs, trackers
AI-powered data entry
Data return and personalized digital services for study participants
Real-time, longitudinal e-consent management
On demand data without delays.
Your study data is updated in real time, letting sponsors bypass expensive and unnecessary data cuts.
The engine behind the evidence
A living observational ecosystem, powered by integrated compliance
Patients as partners
Our patient app returns data to patients and delivers personalized services to enhance engagement and adherence.
Site accelerators
Investigators and site staff minimize time navigating through disparate, counter-intuitive tools, focusing instead on participants and research.
Designed for precision medicine
Our platform is the sole one used by the FDA for its bioinformatics analysis of cell and gene therapies regulatory approvals.