A single platform to deliver genomics at scale.
Flexible and regulated, built for population genomics
Genomic Data
Clinical Decisions
End-to-end and customised to your needs.
Ingest
Modular data pipelines
Fava gives you a flexible data layer that turns genomic outputs into structured, standardised results ready for interpretation and integration.
- Lab agnostic
We work with data from any lab or sequencing partner across file formats and workflows. - Flexible pipelines
We’ve built a library of modular pipelines to rapidly customise data ingestion for each implementation. - Open standards
We convert genomic data into structured clinical results using standards such as openEHR.
Interpret
Governed knowledge management
Fava provides a governed interpretation layer that applies clinical meaning to structured genomic data, turning results into clear, evidence-based guidance that can be safely maintained over time.
- Guideline-based content
We manage clinical content from trusted sources such as CPIC, NICE and DPWG. - Configurable knowledge base
We co-design the content, structure and wording of results to each implementation. - Version-control and governance
We track content versions, approvals and updates, so every result can be traced back to the guidance used at the time.
Integrate
Interoperable by design
Fava implements an integration layer that delivers structured genomic results into clinical systems and workflows.
- Open integration
We return results through standards such as HL7 FHIR, CDS Hooks and custom APIs. - Workflow ready
We deliver genomic guidance into EHRs, prescribing systems, decision support tools, static reports or patient-facing apps. - Population insights
We structure results so they can support population health, service evaluation, and secondary use.
Structured Genomic Insights
Standards-based interoperability
Fava brings ingestion, interpretation and integration together to deliver structured genomic insights that fit the needs of each health system, clinical workflow and user group.
- Implementation-led
We work with each customer to design a deployment model and governance structure for their project. - Designed around users
We co-design content and workflows with clinicians and participants to maximise adoption and impact - Secure and scalable
We build scalable services focussed on data security, open standards and medical device regulation.
Who we work with
We work with partners across genomic ecosystem to connect data, systems and care.
Health systems
Delivering population genomics services
Research programmes
Returning results to clinicians and participants
Laboratory providers
Supporting end-to-end clinical implementation
Sequencing partners
Creating value through clinical impact
EHR and clinical system suppliers
Enabling digital personalised care at scale