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Evidence-led laboratory systems audited under ISO 13485, IVDR readiness, and IEC 62304 software controls.

Connected laboratory instruments in a clinical diagnostics lab

Healthcare in 2030. Engineered today.

Agilent builds analytical and laboratory infrastructure for organizations that cannot separate measurement quality from clinical accountability.

Roadmap to 2030

From instrument excellence to connected evidence systems.

Agilent's next decade is shaped by a simple premise: clinical decisions need analytical accuracy, traceable consumables, secure software, and service data that can be reviewed in one chain. The roadmap below turns that premise into operational milestones for hospitals, reference laboratories, pharma QC groups, and decentralized monitoring teams.

  1. SBOM-by-default

    Software Bill of Materials available for connected instrument families and laboratory data systems.

  2. FHIR and HL7 expansion

    Bidirectional order/result pathways extended across middleware and enterprise LIS deployments.

  3. Automated validation packets

    Instrument, assay, and consumable evidence packaged for easier CLIA and CAP audit preparation.

  4. Remote-commissionable workflows

    More installation, software, and verification steps handled remotely with controlled on-site checkpoints.

  5. Lower-carbon installed base

    Energy, packaging, and parts logistics reviewed as part of lifecycle management for lab fleets.

Milestones that shaped the Agilent laboratory standard.

  1. Agilent begins operating as an independent measurement company with deep analytical instrument expertise.

  2. Expanded life-science systems establish stronger chromatography, spectroscopy, and sample preparation programs.

  3. Clinical and diagnostics workflows become a larger part of laboratory platform strategy.

  4. Connected service, software control, and consumables traceability become central to enterprise laboratory adoption.

  5. Agilent continues aligning laboratory performance, documentation, cybersecurity, and sustainability expectations.

Collaboration model

Built for cross-functional clinical teams.

Agilent projects often involve laboratory directors, clinical chemists, molecular scientists, IT security teams, quality managers, value-analysis committees, and field service leaders. The work succeeds when every stakeholder sees the same performance evidence and the same operational risk picture.

Laboratory MedicineBiomedical EngineeringRegulatory AffairsIT SecurityProcurement

Co-develop the next-generation diagnostic workflow with Agilent.

Start with your test menu, result volume, interface environment, and compliance priorities. We will shape a practical pathway from evaluation to lifecycle support.

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