Augments, not replaces
All flagged signals are routed to the treating physician. The physician retains full clinical authority.
A clinician-facing decision support system that flags patient profiles warranting clinical screening consideration across six cancers. Live in the UAE under Department of Health Abu Dhabi commercial investigation authorization. Regulatory pathways in preparation in North America and Europe.
The BioTwin Cancer Screening Program is a Clinical Decision Support System (CDSS) that provides front-line clinicians with risk summaries derived from BioTwin's multi-omics, lifestyle, and longitudinal data. Designed to support, not replace, clinical judgment.
BioTwin routes flagged profiles to the treating physician with a structured summary. The physician reviews, validates, and decides whether a formal screening pathway is warranted.
All flagged signals are routed to the treating physician. The physician retains full clinical authority.
Models are grounded in peer-reviewed biomarker research and validated through prospective clinical pilots.
BioTwin does not tell the clinician 'this patient has cancer'. BioTwin says 'this patient's profile warrants your clinical judgment regarding screening'.
Active under commercial investigation authorization from the Department of Health Abu Dhabi.
Regulatory pathway in preparation with Health Canada.
FDA pathway in preparation, dual-track approach.
EMA pathway in preparation.
Every public communication about the Screening Program states its regulatory status explicitly. The program is not available for commercial clinical use in any jurisdiction outside the UAE today.
Six cancers today. Expansion follows BioTwin's 5-10-15 roadmap: five clinical domains, ten drops, fifteen health conditions.
Multi-domain risk stratification with low-friction at-home collection.
Repeat measurements, trend analysis, drift detection over time.
Risk stratification across patient populations to support triage and resource allocation.
When a Cancer Risk Program user has a profile warranting clinical attention, and is in a jurisdiction where the Screening Program is approved, their designated clinician is notified with a structured risk summary.
The Cancer Screening CDSS uses the same virtual twin infrastructure as the Cancer Risk Program, and adds validated clinical biomarker models developed in partnership with peer-reviewed research.
| Cancer Risk Program | Cancer Screening Program (CDSS) | |
|---|---|---|
| Regulatory category | Non-medical | Clinical Decision Support System |
| Who uses it | The user | The clinician |
| Where available | Globally | UAE; pending elsewhere |
| Output | Risk score and prevention plan | Structured clinician summary and screening flag |
| Claim | Stratifies cancer risk against published guidance | Supports clinical judgment regarding screening |