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.
We build oncology software — regimen and staging workflows, infusion scheduling, and trial matching — engineered for cancer care and handled to HIPAA standards.
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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.
A oncology platform — clinical workflow, icd-o / tnm cancer staging, and connected integrations — with PHI handled to HIPAA standards at every layer.

The problem
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.
A oncology capability set engineered for its real workflows, codes, and devices.
Protocol-driven chemotherapy regimen logic with dosing checks and safety guardrails.
TNM and ICD-O staging captured as structured, reportable data.
Eligibility matching against staging and molecular markers from the EHR and labs.
Molecular and lab result ingestion tied to the patient record.
Infusion-chair scheduling and care-plan orchestration across the cancer center.
Integration with oncology EHRs and the enterprise record via FHIR/HL7.
Where it fits
Oncology practices, cancer centers, and precision-oncology startups.
Oncology groups modernizing clinical and administrative workflows.
Oncology-focused products going to market.
Oncology device companions, data pipelines, and companion apps.
Oncology programs, care management, and value-based initiatives.
Oncology practices, cancer centers, and precision-oncology startups choose us because we build oncology software that fits the workflow, not the other way round.
Health Insurance Portability and Accountability Act
Protect PHI with privacy-first architecture, encrypted storage and transmission, strict access controls, and traceable audit logs.
General Data Protection Regulation
Implement lawful consent flows, data minimization, retention controls, and secure processing for sensitive health data.
Fast Healthcare Interoperability Resources
Enable standardized health data exchange across apps, care teams, and systems through robust FHIR-ready APIs.
Health Level Seven International
Support enterprise-grade interoperability with HL7-based integrations for records, events, and clinical messaging workflows.
Health Information Trust Alliance
Align security programs to healthcare-specific control and risk management practices trusted by providers and ecosystem partners.
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.
FDA Software as a Medical Device
Plan software quality, traceability, and documentation pathways for products that may require SaMD review and submission.
Medical Device Regulation (European Union)
Prepare EU market-ready processes for risk classification, evidence tracking, and lifecycle governance under MDR expectations.
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
We prove the core workflow with real users before scaling — clinical fit and adoption decide the outcome.
We map the oncology workflow, the codes and devices involved, and the core job to be done.
We build the core workflow with interoperability and PHI handling engineered in from the start.
EHR, device, and standards integration so the product connects to the systems already in use.
A measured launch tracking adoption and outcomes, then iteration.
Healthcare-only focus, standards-based engineering, and delivery you can hold to account.
We understand the oncology workflow, the codes and devices, and the clinical realities that decide adoption.
HIPAA, SOC 2, and role-based access designed in from the first commit — not retrofitted before launch.
FHIR R4, HL7 v2, DICOM, and SMART on FHIR so what we build connects to your existing systems.
Clear scope, working software early, and accountability throughout the engagement.
Solutions for this specialty
Purpose-built Oncology software across the solutions that matter most.
A specialty-configured clinical data model, tuned to oncology.
Device and wearable data ingestion, tuned to oncology.
Secure video and async visits, tuned to oncology.
FHIR R4 and HL7 v2 interfaces, tuned to oncology.
Patient portal and secure messaging, tuned to oncology.
Scheduling and registration, tuned to oncology.
Guideline and rule engine, tuned to oncology.
Ambient capture and transcription, tuned to oncology.
Specialty data warehouse, tuned to oncology.
Coding and charge capture, tuned to oncology.
Tell us your oncology workflow and goals. We'll return a plan that's clinically credible, interoperable, and built to ship.
contact@agnotic.com
Partnerships
contact@agnotic.com