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    Oncology Software Solutions

    Oncology Software Solutions

    We build oncology software — regimen and staging workflows, infusion scheduling, and trial matching — engineered for cancer care and handled to HIPAA standards.

    HIPAA-ReadyFHIR R4SOC 2Interoperable

    Trusted by global innovators

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    Chibasco
    Fundency
    Lantimer
    Lauren
    Lera
    One Minute
    Pento Pix
    TAP
    Xtrium
    Healthevolve
    Benchmark
    Chibasco
    Fundency
    Lantimer
    Lauren
    Lera
    One Minute
    Pento Pix
    TAP
    Xtrium
    Healthevolve
    Benchmark
    Chibasco
    Fundency
    Lantimer
    Lauren
    Lera
    One Minute
    Pento Pix
    TAP
    Xtrium
    Healthevolve
    Benchmark
    Chibasco
    Fundency
    Lantimer
    Lauren
    Lera
    One Minute
    Pento Pix
    TAP
    Xtrium
    Healthevolve

    Oncology software, built for real clinical workflows

    Oncology software has to model complex, protocol-driven care — chemotherapy regimens, TNM staging, molecular markers, and clinical-trial eligibility — where a small error carries real clinical weight.

    We build the regimen logic, structured staging, and trial-matching oncology needs, integrated with the EHR and genomics data, with safety and PHI handling engineered in.

    Architecture

    A oncology platform — clinical workflow, icd-o / tnm cancer staging, and connected integrations — with PHI handled to HIPAA standards at every layer.

    Oncology Software Solutions architecture from clinical workflow to integration

    The problem

    Challenges facing oncology teams

    Off-the-shelf products rarely fit oncology — here is where they fall short, and how we build around it.

    Challenge

    Chemotherapy regimen and dosing logic is complex and safety-critical.

    Agnotic approach

    We build protocol-driven regimen support with dosing checks and human-in-the-loop review.

    Challenge

    Trial eligibility and molecular data are scattered across systems.

    Agnotic approach

    We build trial-matching against structured staging and genomic markers pulled from the EHR and lab feeds.

    Challenge

    Staging and outcomes data are unstructured and hard to report.

    Agnotic approach

    We capture TNM/ICD-O staging as structured data so reporting and analytics are possible.

    What we build for oncology

    A oncology capability set engineered for its real workflows, codes, and devices.

    15-Minute Scoping Call

    Regimen & protocol support

    Protocol-driven chemotherapy regimen logic with dosing checks and safety guardrails.

    Structured staging

    TNM and ICD-O staging captured as structured, reportable data.

    Clinical-trial matching

    Eligibility matching against staging and molecular markers from the EHR and labs.

    Genomics & lab integration

    Molecular and lab result ingestion tied to the patient record.

    Infusion & scheduling

    Infusion-chair scheduling and care-plan orchestration across the cancer center.

    Oncology EHR integration

    Integration with oncology EHRs and the enterprise record via FHIR/HL7.

    Where it fits

    Who we build oncology software for

    Oncology practices, cancer centers, and precision-oncology startups.

    Practices & health systems

    Oncology groups modernizing clinical and administrative workflows.

    Digital health startups

    Oncology-focused products going to market.

    MedTech & device makers

    Oncology device companions, data pipelines, and companion apps.

    Payers & programs

    Oncology programs, care management, and value-based initiatives.

    Engineered for oncology

    Oncology practices, cancer centers, and precision-oncology startups choose us because we build oncology software that fits the workflow, not the other way round.

    Protocol-driven
    Regimen and staging logic built safety-first
    Interoperable
    FHIR R4, HL7 v2, and SMART on FHIR by default
    MVP-ready
    Core oncology workflow shipped first, then scaled

    Compliance-First Healthcare App Development Services Backed by Global Standards

    15-Minute Scoping Call
    01HIPAA logo

    HIPAA

    Health Insurance Portability and Accountability Act

    Protect PHI with privacy-first architecture, encrypted storage and transmission, strict access controls, and traceable audit logs.

    02GDPR logo

    GDPR

    General Data Protection Regulation

    Implement lawful consent flows, data minimization, retention controls, and secure processing for sensitive health data.

    03FHIR logo

    FHIR

    Fast Healthcare Interoperability Resources

    Enable standardized health data exchange across apps, care teams, and systems through robust FHIR-ready APIs.

    04HL7 logo

    HL7

    Health Level Seven International

    Support enterprise-grade interoperability with HL7-based integrations for records, events, and clinical messaging workflows.

    05HITRUST logo

    HITRUST

    Health Information Trust Alliance

    Align security programs to healthcare-specific control and risk management practices trusted by providers and ecosystem partners.

    06HITECH logo

    HITECH

    Health Information Technology for Economic and Clinical Health Act

    Design with breach notification readiness, digital record safeguards, and operational controls that support regulated care programs.

    07SaMD logo

    SaMD

    FDA Software as a Medical Device

    Plan software quality, traceability, and documentation pathways for products that may require SaMD review and submission.

    08MDR (EU) logo

    MDR (EU)

    Medical Device Regulation (European Union)

    Prepare EU market-ready processes for risk classification, evidence tracking, and lifecycle governance under MDR expectations.

    09SAMHSA logo

    SAMHSA

    Substance Abuse and Mental Health Services Administration

    Apply confidentiality controls and consent-aware sharing models for behavioral and mental health data experiences.

    Codes, standards & devices

    Oncology standards baked in

    ICD-OFHIRHL7
    Our Process

    How we build oncology software

    We prove the core workflow with real users before scaling — clinical fit and adoption decide the outcome.

    1.

    Discovery & Clinical Design

    We map the oncology workflow, the codes and devices involved, and the core job to be done.

    Workflow-shaped
    2.

    Architecture & Core Build

    We build the core workflow with interoperability and PHI handling engineered in from the start.

    Compliant
    3.

    Integrations

    EHR, device, and standards integration so the product connects to the systems already in use.

    Connected
    4.

    Launch & Iterate

    A measured launch tracking adoption and outcomes, then iteration.

    Adoption-tuned
    Why Partner With Us

    Why oncology teams build with Agnotic

    Healthcare-only focus, standards-based engineering, and delivery you can hold to account.

    15-Minute Scoping Call

    Oncology workflow depth

    We understand the oncology workflow, the codes and devices, and the clinical realities that decide adoption.

    Compliance by default

    HIPAA, SOC 2, and role-based access designed in from the first commit — not retrofitted before launch.

    Interoperable engineering

    FHIR R4, HL7 v2, DICOM, and SMART on FHIR so what we build connects to your existing systems.

    Delivery you can verify

    Clear scope, working software early, and accountability throughout the engagement.

    Frequently Asked Questions

    Yes. We model regimens as ordered cycle-day templates with BSA and carboplatin AUC (Calvert) dosing, cumulative anthracycline and bleomycin caps, and renal or hepatic dose adjustments. Orders enforce pre-medication, hydration, and lab gating before a nurse can release a cycle.

    Ready to build your oncology software?

    Tell us your oncology workflow and goals. We'll return a plan that's clinically credible, interoperable, and built to ship.

    Email

    contact@agnotic.com

    Partnerships

    contact@agnotic.com