Our approach to privacy
Your history.
Your control.
Health information deserves care at every step. We're building DiaGraph around consent, traceable information and clear boundaries between patient and clinician views.
Start with synthetic data.
Development and evaluation use synthetic records and hand-written notes. Real patient data is not needed for the research prototype. This website does not offer health-record uploads or clinical services.
Access through consent.
The product is being built for time-limited patient consent before a clinician can access the full record and reasoning. Access rules and an audit trail are planned at the database level.
Two views, with clear boundaries.
Patients will see their own history in plain language, with sources they can check. Ranked diagnoses and high-risk links are reserved for the clinician view. Clinicians remain responsible for decisions about care.
Trace every connection.
Findings retain their source text. Uncertain information waits for review, and proposed additions to the medical graph require supporting evidence and clinician approval.
Review before real-world use.
Privacy and medical-device requirements are part of the research plan, including legal review with the law faculty. These are design commitments for a product in development, not a claim of regulatory approval or certification.
This website.
The theme toggle saves your light or dark preference in your browser. Links to external resources take you to websites with their own privacy practices.
This page describes our approach to development. A policy covering the eventual health-data service will be needed before that service launches.