AI is assistive, not autonomous
AI outputs are structured drafts for screening workflow—not diagnoses or treatment decisions.
DeeponVision is built around a human-in-the-loop model. AI outputs are treated as draft screening support and require review by an ophthalmologist before they are used in patient-facing reports.
AI outputs are structured drafts for screening workflow—not diagnoses or treatment decisions.
An ophthalmologist reviews, approves, modifies, or rejects AI-assisted output before patient-facing use.
The workflow checks recorded patient consent before sending medical data to configured external AI providers.
Organization records are scoped by clinic and protected through policies and route authorization.
Uploaded eye images and reports are stored privately and served only through authenticated routes.
Sensitive workflow events such as uploads, downloads, reviews, PDFs, and settings changes are recorded.
Staff can prepare the record, while qualified doctors remain responsible for interpretation and clinical decisions.
Product copy and reports explicitly state that AI-assisted output is not a medical diagnosis.
Every external provider requires privacy, legal, clinical, and data-processing review before production use.
DeeponVision does not replace ophthalmic devices, imaging systems, or clinical judgment. AI-assisted summaries require doctor review before patient-facing use.
Clinics can test with mock AI, connect internal FastAPI experiments, or configure external providers only where consent, privacy, licensing, and regulatory requirements are satisfied.
Structure a screening summary and suggested review action.
Interpret findings, confirm diagnosis, and choose treatment.
Validate providers, consent, security, compliance, and clinical use.
Explore the platform’s safeguards and discuss your organization’s governance requirements.
Request a Demo