A SaaS platform that helps health tech startups design, manage, and publish clinical validation studies — protocol templates, IRB workflows, data collection, and AI-powered statistical analysis.
Get My Free Checklist →"Medicine would be terrifying if it tried to be just like tech. However, I feel that many of the collaboration efforts pioneered in software development could be hugely beneficial."
"I am an MD and all of our training is focused on learning medicine and there is very little in the way of business or entrepreneurship taught in school."
"Healthcare entrepreneurship deserves more light. The intersection of medicine and technology is where the most impactful innovations will happen."
Pre-built study protocol templates for common health tech validation needs — RCTs, observational studies, pilot studies, and user outcome analyses.
Guided IRB application builder with auto-populated forms, consent templates, and submission tracking across major IRB platforms.
Secure participant enrollment, survey deployment, and data capture tools designed for health tech validation — HIPAA-compliant from day one.
Upload your data and get publication-ready statistical analysis with appropriate tests, effect sizes, and confidence intervals — no biostatistician required.
Manuscript templates, journal matching, and submission guides to turn your results into peer-reviewed publications that drive credibility.
Auto-generated clinical evidence summaries designed for pitch decks, hospital sales, and regulatory submissions.
Tell us what your product does and what you need to prove. We'll recommend the right study design.
Use our templates and guided builder to create an IRB-ready study protocol in days, not months.
Enroll participants, collect data, and run AI-powered statistical analysis with publication-ready outputs.
Generate investor reports, manuscript drafts, and regulatory summaries from your validated results.
Every protocol template is designed by clinical researchers. Your study will meet the standards of peer-reviewed journals.
Participant data is encrypted, access-controlled, and audit-trailed. Built for the regulatory environment from day one.
Designed by someone who understands both clinical research and startup constraints. Get clinical proof without CRO budgets.
Your free checklist is on its way to your email. Check your inbox (and spam folder) in the next few minutes. We'll also send you actionable insights based on the latest research.