The Enablement Layer
for Clinical Trials
A direct line from protocol to patient: treating physicians, infusion centers, specialty pharmacies, and community practices unified in one accessible research platform.
A direct line from protocol to patient: treating physicians, infusion centers, specialty pharmacies, and community practices unified in one accessible research platform.
of eligible patients are ever considered for a clinical trial.
of U.S. physicians run trials. The patients and chairs exist; the infrastructure doesn't.
per day is what enrollment delays cost sponsors.
Not a recruitment problem.
An access problem.
Control from the onset.Control, where there was none.
Your protocol, matched against 40M+ real patient records: exactly how many patients qualify, where they're treated, and how to enroll them. Before you commit to a design, a site list, or a timeline.
Test draft criteria against real records before design lock, and avoid the amendments that cost months later.
Select sites on verified counts of eligible patients, reaching patient populations and site infrastructure previously inaccessible or unknown to your organization.
Eligible patients are found before activation and invited through their own physicians. Faster first-patient-in, fewer screen failures.
Immunology, oncology, rheumatology, neurology, ophthalmology: today's pipeline is infusion-delivered, and sponsors, CROs, and site networks are competing for the patients you already treat. We surface the studies your population qualifies for and bring those trials to your centers, with the support to run them.
The matching is done for you. Opportunities arrive scoped to patients you already treat, and you choose which to accept.
Offer tomorrow's therapies in your own chairs, instead of losing patients to academic centers.
The scarcest resource for sponsors and CROs is infusion-capable sites with the right patients. That's your network.
Matching runs inside the EHR you already use. Eligible patients surface right in the schedule, and they hear about research from the doctor they already trust.
Eligible patients surface in your schedule, visit by visit, without chart reviews or registries.
Trial opportunities without the administrative burden. Readiness, training, and regulatory built with you.
A new care option for your patients and a new revenue line for the practice, at no cost to you.
Hover or tap a capability to see it in the window.
Embedded in the systems sites, sponsors, and CROs already run. Activation is plug-and-play.
Full eligibility computed against real records: labs, medications, chart notes, and documents.
91% Site–Trial Match. How well your site's patient panel aligns with this study's eligibility criteria.
Standardized readiness scoring, then the build to sponsor-viable: training, regulatory, and workflows.
Message matched patients, coordinate scheduling, and deliver trial education, directly from the practice.
Share one protocol or patient population with us, and we'll show you what real access looks like, no commitment required.