Frequently asked questions
Common questions from hospitals, NGOs, ministries of health, and research partners.
Is AccuVis FDA or CE approved?
AccuVis is currently in evaluation and regulatory development. CDSCO SaMD registration is in progress. The platform is intended for research and evaluation until applicable regulatory clearance is obtained in your jurisdiction. See our disclaimer.
Does AccuVis replace a radiologist?
No. AccuVis provides pre-read assistance and decision support. All outputs require review by a qualified healthcare professional before clinical action.
What image formats are supported?
DICOM (.dcm), JPEG, PNG, BMP, and TIFF. Study metadata can auto-populate clinical inputs for risk fusion.
What deployment options are available?
Cloud and on-premises options are available for hospitals and national programs that require data sovereignty. Analysis requires an active network connection — AccuVis does not run in offline mode.
How is patient data handled?
Images are processed for analysis only and are not persisted on our servers. See our privacy policy. Data Processing Agreements are available on request.
Does AccuVis integrate with PACS or EHR systems?
AccuVis accepts DICOM and standard image formats and is designed to fit hospital imaging and screening workflows. Contact us to discuss integration with your PACS or programme systems.
What is the pricing model?
We offer pilot, hospital, and enterprise licensing — per-scan and site-licence options. Contact us for pricing based on your volume and deployment model.
What conditions does AccuVis support?
Four clinical pathways: lung cancer, tuberculosis, pneumonia, and cardiovascular risk — plus a fused 0–100 lung risk score. See the product page for details.
Has AccuVis been validated on African or Indian populations?
AccuVis is developed and validated for clinical use in diverse settings. Prospective validation on African and South Asian populations is in progress. See impact & evidence or request a validation report.
How do I get console access?
Console access is invite-only. Request credentials via our contact form or LinkedIn. Provisioned users receive a direct link to the clinical console.
How do I schedule a demo?
The fastest way is to message us on LinkedIn or use the contact form. We respond within two business days.
Where is AccuVis based?
AccuVis AI is headquartered in Bengaluru, India, serving healthcare programs across Africa and India.
Still have questions?
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