The intelligent research platform built for health systems
Bringing innovation within reach of every patient.
Research teams are stretched thin.
Coordinators spend hours on manual chart review. Eligible patients slip through the cracks. Studies under-enroll while matching patients sit in your EHR, invisible.
Let Lind do the heavy lifting.
Watch Lind prescreen a real patient criterion by criterion, with evidence pulled straight from the chart.
Right patient, right trial, at scale.
Automated screening across every patient and every study — embedded in your EHR.
Surface eligible patients
Screening across every patient in your system. Trial-arm level match scoring, embedded directly in the EHR with zero disruption to clinical workflows.
- Works across all indications
- Screen for all studies at your health system
- Easy to navigate and filter to find the best options
Pre-screen with confidence
Expert-level criteria matching powered by AI, with source evidence pulled directly from the patient record. Every decision is explainable and auditable.
- Explanation with links directly into the health record
- Decision deferred to users when clinical judgment is required
- Absence of evidence and evidence of absence highlighted
Powering an intelligent site network
Every health system on the Lind Platform adds to a growing network of research-ready sites with verified patient populations. For sponsors, that means faster enrollment, better site selection, and studies designed around real-world data — not guesswork.
Stronger sites. Smarter protocols. Powered by real-world data.
Run your trials on the Lind network. Real-world patient data and site-level intelligence to accelerate enrollment and de-risk study design.
Activate high-quality sites
Identify the right sites before study startup. Real-world patient density data across the Lind network helps you select higher-performing sites and compress time to enrollment.
- Real-world patient density by site
- Data-driven site selection and ranking
- Accelerated study startup
Optimize trial protocols
See which eligibility criteria are filtering out patients before enrollment starts. Cohort modeling and per-criterion insights help de-risk study design.
- Per-criterion eligibility insights
- Cohort modeling and bias reduction
- Protocol rescue for under-accruing studies
Clinically validated.
Operationally effective.
Accuracy that matches expert physicians, deployed at enterprise scale across real health systems.
Clinically validated
- 97% screening accuracy validated against expert oncologists at major academic centers
- Peer-reviewed: in-review with JCO and ASCO; presented at AACR; NCI co-publication
- Production-scale: 224K+ patient records processed across 90+ active studies daily
Deployed at scale
- Live with 3 health system partners covering 17M patients across 86 hospitals
- Disease-agnostic: oncology, dermatology, hematology, neurology and expanding
- FHIR-native integration with multiple EHR platforms, data-source agnostic by design
Every patient deserves to know about the trial that could save their life
Today, 91% never do.
No more invisible patients.