BioTwin Oncology

Cancer Screening Program

Clinical Decision Support System (CDSS)

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.

Section 1

What it is

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.

Section 2

Clinical positioning

Augments, not replaces

All flagged signals are routed to the treating physician. The physician retains full clinical authority.

Evidence-based

Models are grounded in peer-reviewed biomarker research and validated through prospective clinical pilots.

Decision support, not diagnosis

BioTwin does not tell the clinician 'this patient has cancer'. BioTwin says 'this patient's profile warrants your clinical judgment regarding screening'.

Section 3

Regulatory status

  • UAE
    Live

    Active under commercial investigation authorization from the Department of Health Abu Dhabi.

  • Canada
    In prep

    Regulatory pathway in preparation with Health Canada.

  • United States
    In prep

    FDA pathway in preparation, dual-track approach.

  • European Union
    In prep

    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.

Section 4

Scope

Six cancers today. Expansion follows BioTwin's 5-10-15 roadmap: five clinical domains, ten drops, fifteen health conditions.

Lung
Pancreatic
Colorectal
Breast
Prostate
Ovarian
Section 5

How it fits into a clinical workflow

01

Preventive screening

Multi-domain risk stratification with low-friction at-home collection.

02

Longitudinal monitoring

Repeat measurements, trend analysis, drift detection over time.

03

Population health management

Risk stratification across patient populations to support triage and resource allocation.

04

Physician notification

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.

Section 6

The science

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.

Section 7

Distinction from the Cancer Risk Program

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

Talk to the BioTwin clinical team.

Primary care, specialist, hospital, or health system. BioTwin designs pilots around your patient population and clinical goals.