LifePath OI Ecosystem

DSK V1.0

Commercial Overview · Organic Intelligence Group LLC © 2026

The Problem We Solve

Regulated industries (healthcare, finance, public sector) cannot deploy AI decisions that change their answer for identical input. Today's LLM-driven systems are probabilistic: same prompt, different outcome. That non-determinism fails every audit, breaks compliance, and makes every automated decision legally indefensible.

DSK V1.0 is a deterministic decision kernel: identical input always yields identical, hash-verifiable output. It is the missing infrastructure layer for decisions that must be reproducible, auditable, and provable in a court of law.

Market · Where DSK Applies

Regulated decision systems where every automated outcome must be reproducible on audit.

Target Market

Healthcare

Clinical triage, prior-auth, drug-interaction decisions under HIPAA & FDA Part 11.

Finance

Credit adjudication, AML alerts, trade-surveillance determinism for SOX & SR 11-7.

Public Sector

Benefits eligibility, visa adjudication, automated compliance under OMB / EU AI Act.

Addressable: regulated decision systems where every automated outcome must be reproducible on audit.

Pricing · How It Sells

Three commercial paths — per-decision usage, enterprise license, and supervised bridge access.

Pricing Model

Per-Decision

Usage-priced kernel resolutions for pilots & evaluation tiers.

Enterprise License

Annual platform license with governed bridge access for in-house teams.

Bridge-Access Tier

Time-boxed, supervised engineer connections for integration & verification.

3-Year Adoption Ramp (Estimate)

Year 1

2–3 design-partner pilots in healthcare & finance; bridge-access revenue; reference deployments.

Year 2

Enterprise licenses in regulated verticals; first public-sector eligibility deployment.

Year 3

Platform scale across regulated decision systems; per-decision volume economics.

Estimates only — directional, not guidance.

Why Now · Regulatory Tailwind

Live mandates now require traceability, reproducibility, and auditability for high-risk automated decisions.

Why Now

EU AI Act

High-risk AI systems require traceability, reproducibility, and auditability — live 2026.

FDA 21 CFR Part 11

Electronic decision records must be reproducible and tamper-evident for regulated devices.

HIPAA Determinism

Clinical decision support acting on identical input must produce identical, auditable output.

These are live regulatory tailwinds — regulated buyers now have a compliance mandate to procure determinism.

Pilot Pipeline (Placeholder)

Clinical Triage (Healthcare)

In discussions — target design partner

Credit Adjudication (Finance)

Target vertical — outreach Q4

Benefits Eligibility (Public Sector)

Target vertical — monitored RFP pipeline

Placeholder — concrete pilot verticals and status to be updated as engagements solidify.

IP-Safe Commercial Overview — Organic Intelligence Group LLC © 2026