How it works
From kickoff to leads in your system.
A clear, IRB-first workflow. Nothing runs until your materials are approved, and every lead arrives with its consent and source.
The five-step workflow
Creative
We build study-specific ad concepts and a plain-language study page.
IRB review
Your IRB reviews and approves the materials before anything runs.
Launch
Geo-targeted Meta campaigns go live to the regions and audiences that fit your protocol.
Delivery
Consented leads reach your coordinators securely — by signed webhook or authenticated pull, with provenance.
Disposition
We track outcomes so spend stays on what actually enrolls.
Where the boundary sits
We develop creative and deliver leads. Research sites perform eligibility screening and informed consent under their own IRB-approved process. Patient-facing intake is not hosted on this site; per-study information pages are published per engagement, bound to approved materials.