AI-powered clinical decision support and genomics analytics infrastructure for health systems and labs.

FlahyCDS helps enterprises and diagnostic laboratories identify clinically actionable genomic opportunities, support appropriate test utilization, and convert biological signals into clinician-ready reports.

Built for real-world care delivery, FlahyCDS combines clinical logic, guideline-based decision support, AI-assisted identification of actionable care opportunities, AI-guided patient readiness pathways, and genomic analytics to support the right test, for the right patient, at the right time.

Areas of Use

Health Systems

FlahyCDS uses AI to identify clinical windows where advanced testing can have the greatest impact — surfacing patients whose next care decision could meaningfully change based on diagnostic insights.

Pre-Test Readiness

Guides patients directly through an interactive, AI-guided readiness pathway that helps determine when standard care may be falling short, educates them on advanced testing, and supports informed consent for personalized treatment design.

Clinician Workflows

Connects patient readiness, consent, and clinical context to support clinical decision-making, helping care teams identify advanced testing opportunities and shape more personalized treatment plans.

FlahyCDS is currently free for individual clinicians to use. Sign up here ()

Laboratories

FlahyCDS gives laboratories a comprehensive genomic interpretation platform that translates complex data, including proprietary markers, into actionable clinical insights for general practice, internal medicine, oncology, neurology, psychiatry, and other genomics workflows.

How FlahyCDS Works

FlahyCDS step 1

Determines when testing changes management

Applies clinical logic to judge whether advanced testing would meaningfully alter this patient's next step — flagging the moments that matter and filtering out the ones that don't.

FlahyCDS step 2

Reads the clinical context

Pulls together genomic signals, diagnosis, history, and presentation into one patient picture — the inputs a decision actually depends on.

FlahyCDS step 3

Resolves the result into a decision

Interprets findings, including proprietary and specialty markers, against guideline logic — producing not just a report, but a clear recommendation on what to do next.

End-to-End Genomics Decision Infrastructure

FlahyCDS provides the secure workflow layer that enterprises and laboratories need to deploy clinical decision support and genomics at scale.

From identifying the right clinical windows for advanced testing to interpreting genomic data and generating clinician-ready reports, FlahyCDS brings the core components of genomics decision support into one scalable platform.

Built for privacy-sensitive, high-volume environments, FlahyCDS helps organizations bring genomics into clinical and laboratory workflows without building the full decision support, interpretation, and reporting infrastructure from scratch.

Identify
Interpret
Report

Deploy FlahyCDS

Request a demo to explore how FlahyCDS can support your health system, laboratory, or genomics program.

Interested in enterprise or laboratory deployment? Tell us about your organization.