Launch Sponsored Protocols in Minutes
Our AI agents generate complete study protocols, informed consent documents, and patient communications — tailored to your specific intervention.
Benefits to Sponsors
Everything you need to run professional observational studies — without the traditional overhead
Physician Oversight
Every protocol is reviewed and overseen by a licensed MD to ensure clinical validity and participant safety.
Human Study Coordinator
Dedicated coordinators manage participant communications, safety alerts, and data quality — not just bots.
Aggregate Data & Insights
Access de-identified aggregate outcomes data for marketing claims, product development, and clinical validation.
White-Label Branding
Brand the study experience with your company logo, colors, and messaging for seamless patient engagement.
IRB-Ready Documentation
AI-generated protocols and consent documents follow FDA and IRB requirements out of the box.
Launch in Days, Not Months
Skip the traditional 6-12 month protocol development cycle. Go from concept to live study in under a week.
How It Works
From intervention to live protocol in four simple steps
Define Intervention
Enter the treatment or intervention you want to study. Our AI handles the rest.
AI Generates Protocol
Our Protocol Agent designs endpoints, PRO instruments, and safety thresholds.
Invite Participants
Participants complete consent, screening, and baseline surveys on mobile.
Collect Data
Track outcomes with validated PRO instruments and integrate lab results.
AI-Powered Protocol Design
Validated PRO Instruments
qADAM, IIEF-5, PHQ-2, and other validated questionnaires selected for your intervention.
Auto-Generated Consent
Plain-language informed consent documents with comprehension verification.
Safety Monitoring
Automatic alerts when participants exceed safety thresholds on PROs or labs.
Smart Engagement
AI-crafted reminders and milestone messages to maximize participant retention.