Health plans
Medical claim adjudication across commercial and government lines.

We build claims engines that ingest EDI 837, adjudicate against plan rules, and return 835 remittance with minimal human touch, plus a denial-prediction model that flags problems before they become appeals.
Trusted by global innovators
























Claims processing automation is software that takes a health care claim from EDI 837 intake through eligibility, benefit and pricing rules to a payment or denial decision, with as little manual handling as the plan rules allow. Agnotic Technologies builds these engines for payers, TPAs and self-funded plans, with every automated decision logged for audit.
The bottleneck is rarely the payment: intake parsing, eligibility and benefit matching, plan-rule evaluation and pended-claim triage eat examiner hours. We raise the straight-through-processing rate with validated EDI 837 intake, a transparent rules engine, reasons on every pended claim and denial prediction upstream.
What it is
Claims processing automation takes an inbound claim from EDI intake through eligibility, benefit, and pricing evaluation to a payment or denial decision, with as little manual handling as the plan rules allow.
The measure of success is the straight-through-processing rate and the accuracy of the automated decisions. We build engines that are both fast and explainable, so examiners handle genuine exceptions and every decision withstands audit.
Auto-adjudication, rules transparency, and denial prediction in one pipeline, so examiners work the exceptions, not the routine.

Each capability pairs an automation outcome with the EDI standard or rule mechanism behind it.
Inbound professional, institutional, and dental claims parsed from the X12 5010 837 format, validated against structural and business edits, with 999 and 277CA acknowledgments returned to submitters automatically.
A transparent rules engine that evaluates eligibility, benefits, provider network status, and pricing to adjudicate clean claims straight through, pending only the ones that genuinely need an examiner.
A model that scores incoming claims for denial likelihood by procedure, diagnosis, and provider pattern, surfacing correctable issues before adjudication so avoidable denials never hit the appeal pipeline.
Electronic remittance advice produced in the X12 835 format with accurate CARC/RARC reason codes, adjustments, and payment details reconciled to the adjudication result.
Duplicate-claim logic, unbundling and upcoding flags, and anomaly detection integrated into the adjudication flow, with a full audit trail on every automated decision.
Pended claims routed with a plain-language reason and the rule that triggered them, plus dashboards for STP rate, turnaround time, and denial categories to tune the engine over time.
Where it runs
Medical claim adjudication across commercial and government lines.
Multi-client adjudication with plan-specific rule sets.
Automated processing for self-insured benefit plans.
Specialty adjudication with 837D and plan-specific benefit logic.
Coordinated adjudication alongside medical claims.
High-cost claim identification and downstream reporting.
The lever is straight-through-processing rate. We instrument it end to end so gains are measurable: targets are validated against your claim mix in discovery.
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 standards-based FHIR 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.
Standards we build against
Intake, rules, and remittance are built and validated in parallel against real 837 samples.
We map your plan designs, current STP rate, pend reasons, and examiner workload, then design the rules model and the automation boundary before building.
We build 837 intake, validation, and the auto-adjudication rules engine, testing against real claim samples to confirm decisions match your policy.
The denial-prediction layer and 835 generation, with the examiner workbench for the exceptions the engine intentionally pends.
Phased launch with STP-rate and turnaround dashboards, plus ongoing rule and model tuning as plan designs evolve.
Short facts we design claims engines around, each linked to its primary source.
HIPAA adopts ASC X12 standards for electronic transactions, including health care claims (837), payment and remittance advice (835), eligibility inquiries (270/271) and prior authorization requests (278).
Source: 45 CFR Part 162 (eCFR)A HIPAA covered entity may share protected health information with a business associate, such as a software vendor, only under a business associate agreement that commits the vendor to safeguard it.
Source: 45 CFR 164.502(e) and 164.504(e) (eCFR)The HIPAA Security Rule requires administrative, physical and technical safeguards for electronic protected health information.
Source: 45 CFR Part 164 Subpart C (eCFR)The NIST AI Risk Management Framework is a voluntary framework that organizes AI risk work into four functions: Govern, Map, Measure and Manage.
Source: NIST AI 100-1Related proof of compliant delivery: Lera Health is a patient-facing platform, not a claims engine, but building its secure, auditable data layer demonstrates the PHI handling and decision-traceability rigor an adjudication system requires.

We bring EDI adjudication depth and explainable-automation engineering so your STP rate rises without losing auditability.
Every automated decision carries the rule and data that produced it, built for compliance review, not opaque black-box logic.
837 intake, 835 output, CARC/RARC semantics, and pricing logic are our starting point, not a learning curve billed to you.
We target measurable straight-through-processing gains validated against your real claim mix, not demo data.
Prediction and adjudication that examiners can understand and override, so trust in the system grows instead of erodes.
Adjudication that scales without losing the audit trail
Tell us your plan designs and current STP rate. We'll return a claims-automation plan with rules scope, prediction approach, and a realistic timeline.
contact@agnotic.com
Partnerships
contact@agnotic.com