Custom Software

Oncology AI Software Development

Oncology is where healthcare AI has the strongest clinical evidence and the most demanding integration requirements. Treatment matching against the NCCN guidelines, biomarker-based therapy selection, clinical trial eligibility screening, and tumor board decision support all run on a stack that combines structured EHR data, unstructured pathology and radiology reports, genomic test results, and a regulatory pathway that often crosses the FDA SaMD threshold. Generic AI engineering does not get you there.

Taction Software’s oncology AI engineers have built treatment-matching engines, trial-eligibility screeners, and biomarker analytics pipelines integrated with Epic, Cerner, and other major EHRs. We work with NCCN guidelines, OncoKB, ClinicalTrials.gov data, and FHIR R4 oncology profiles. Engagements begin with a $45K Discovery Sprint.

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When to Use Oncology AI Development Services

01

Use Oncology AI When

  • You are building treatment-matching, trial-eligibility, or biomarker analytics
  • You are an academic medical center building internal oncology AI
  • You are a digital health company selling oncology AI to cancer centers
  • You are a pharma company building patient-matching for trials
  • You are a MedTech company on the FDA SaMD pathway for oncology software
Recognition

Awards & Recognitions

Clutch AI Award
Top Clutch Developers
Top Software Developers
Top Staff Augmentation Company
Clutch Verified
Clutch Profile

Why Oncology AI Requires Specialized Engineering

  • Multi-modal data — structured EHR plus unstructured pathology, radiology, and genomics
  • NCCN guideline integration — treatment recommendations need to map to the current NCCN compendium
  • Genomic variant interpretation — OncoKB, ClinVar, COSMIC, and biomarker-driven matching
  • Clinical trial eligibility — ResearchSubject and ResearchStudy FHIR resources tied to ClinicalTrials.gov
  • FDA SaMD pathway — many oncology AI features cross the SaMD threshold
  • Tumor board workflows — multidisciplinary decision-support patterns
  • Cancer registry data — SEER, AJCC staging, ICD-O-3 morphology and topography codes

What Oncology AI Actually Touches

  • FHIR R4 oncology profiles including Condition, Observation, Procedure, MedicationStatement
  • NLP over pathology and radiology reports
  • Genomic data normalization
  • NCCN guideline matching logic
  • Clinical trial eligibility computation
  • AI inference layer with BAA-covered providers
  • Audit logging at HIPAA §164.312(b) granularity

Our Oncology AI Development Approach

Phase 1: Discovery — $45K, 4 Weeks

We map your oncology AI use case (treatment matching, trial eligibility, biomarker analytics, tumor board support), select the data sources, identify FDA SaMD risk, and produce a technical architecture with eval harness skeleton and BAA-eligible model path.

Phase 2: MVP Sprint — $95K, 8 Weeks

We build the inference pipeline with PHI redaction, the NCCN or biomarker matching logic, FHIR integration, the first end-to-end use case, and audit logging.

Phase 3: Pilot-Ready — $145K, 12 Weeks

We harden for clinical pilot, produce clinical evidence, prepare FDA SaMD documentation if applicable, and produce care-package handoff.

For productized sprint pages, see Discovery Sprint, MVP Sprint, and Pilot-Ready Sprint.

Oncology AI Patterns We Have Shipped

  1. 01

    Treatment Matching Against NCCN

    AI-powered treatment-pathway matching based on stage, biomarker, prior therapy, and comorbidity.

  2. 02

    Clinical Trial Eligibility Screening

    Automated trial-eligibility computation across ClinicalTrials.gov, tied to FHIR ResearchSubject and ResearchStudy.

  3. 03

    Pathology Report NLP

    Structured extraction from free-text pathology reports including tumor type, grade, margin status, lymph node involvement, and biomarker results.

  4. 04

    Radiology Report NLP for Oncology

    RECIST measurement extraction, lesion tracking across studies, and tumor burden assessment.

  5. 05

    Genomic Variant Interpretation

    Integration with OncoKB and ClinVar for biomarker-driven therapy matching.

  6. 06

    Tumor Board Decision Support

    Multidisciplinary case-presentation AI with treatment-option ranking and evidence summarization.

    For background, read our healthcare AI use cases 2026 guide and the HIPAA-compliant AI engineers playbook.

Engagement Models and Pricing for Oncology AI

HIPAA and AI Compliance Baseline

  • BAA executed with Taction and every model provider before any PHI is processed
  • BAA-eligible model providers only — see our BAA with AI providers guide
  • PHI redaction at inference
  • Audit logging at the FHIR and inference layers
  • FDA SaMD pathway readiness — see our FDA SaMD pathway add-on
  • Encryption at rest with AES-256 and in transit with TLS 1.3
FAQs

Frequently Asked Questions About Oncology AI

Discovery Sprint $45K, MVP Sprint $95K, Pilot-Ready Sprint $145K. Full pathway $285K over 24 weeks.

Frequently yes. Treatment-matching engines and biomarker-driven recommendations often qualify as Software-as-a-Medical-Device. We identify this during Discovery and pair the engagement with the FDA SaMD pathway add-on when applicable.

NCCN guidelines, OncoKB, ClinVar, COSMIC, ClinicalTrials.gov, SEER, AJCC staging, ICD-O-3, plus standard FHIR R4 resources.

Yes. Integration with OncoKB, ClinVar, and COSMIC for biomarker-driven therapy matching is standard.

Yes. NLP over unstructured oncology reports is core work, including RECIST measurement extraction and biomarker normalization.

Yes. Multidisciplinary decision-support patterns with treatment-option ranking and evidence summarization are within scope.

Yes. Every engagement begins with a BAA.

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