AI-Powered Research Platform

Launch Clinical Studies in Minutes

Our AI agents generate complete study protocols, informed consent documents, and patient communications — tailored to your specific intervention.

How It Works

From intervention to live study in four simple steps

01

Define Intervention

Enter the treatment or intervention you want to study. Our AI handles the rest.

02

AI Generates Protocol

Our Clinical Protocol Agent designs endpoints, PRO instruments, and safety thresholds.

03

Invite Participants

Participants complete consent, screening, and baseline surveys on mobile.

04

Collect Data

Track outcomes with validated PRO instruments and integrate lab results.

Features

AI-Powered Study 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.

Example Study
Active

TRT Outcomes Study

Duration
26 weeks
Endpoints
4 validated
Lab Markers
3 tracked
PRO Schedule
9 timepoints
Generated in
~2 min
by AI

Ready to launch your study?

Get started in minutes. No protocol writing experience required.