Synthetic Data & Research Use Policy
Effective Date: May 1, 2026 · Last Updated: May 1, 2026
Purpose of This Policy
This page explains, in plain language, what kind of data you see on vitasignal.ai and how it may - and may not - be used. If you have additional questions, please contact us at info@vitasignal.ai.
What Is Synthetic Data?
Every patient name, vital sign, risk score, and clinical scenario shown on the public website and its public demonstration surfaces is computer-generated. Synthetic data is created by algorithms that produce realistic-looking but entirely fictional clinical records. It is not derived from, linked to, or traceable to any real individual.
- No patient data is displayed on the public website or public demonstration surfaces.
- No patient data is stored in the databases backing the public website.
- No patient data is transmitted to or from your browser by this website.
- Separately, approved research work may use de-identified retrospective data under written agreements, applicable approvals, and appropriate controls. That work happens outside this public website and is never displayed here.
Research Use Only
VitaSignal is a pre-market research prototype. Nothing on this website constitutes medical advice, a clinical recommendation, or a diagnostic output. Specifically:
- The platform is not FDA-cleared or approved for any clinical use.
- Risk scores, SHAP explanations, and trend indicators are for research and educational demonstration only.
- No output from this site should influence clinical decision-making of any kind.
Anonymous Usage Analytics
We collect lightweight, anonymous analytics to understand how visitors explore the platform. This data includes:
- Pages visited and filter presets applied.
- Browser type and approximate session duration.
- Referring URL (if any).
No personally identifiable information (PII) is collected. We do not capture your name, email, IP address, or any other identifier through our analytics system. Anonymous analytics events are automatically deleted after 180 days.
Regulatory Classification
VitaSignal is a pre-market research prototype. The regulatory pathway is under evaluation. The public website and public demonstration surfaces do not acquire, process, or analyze medical images or signals from hardware devices. Public outputs are illustrative and support governance discussion only. They are not available for patient-care or clinical decision-making.
Questions?
If you have questions about this policy, our use of synthetic data, or our research program, please reach out:
- Email: info@vitasignal.ai
- Licensing inquiries: licensing@vitasignal.ai
Related: Privacy Policy · Terms of Use · Trust Center