The regulated-supply-chain compliance engine
One compliance engine.
Earned one vertical at a time.
A single industry-agnostic compliance engine that powers every regulated supply chain — pharma today, food and med-device tomorrow, every standards-governed industry in time — earned one vertical at a time.
Designed for your regulatory reality
- 21 CFR Part 11supports
- EU GMP Annex 11aligned
- ICH Q10aligned
- GAMP 5 Category 4classified
- ALCOA+designed-in
- ISO 19011aligned
Precise stances, not certification claims — details on the Trust page.
Why not a “horizontal platform”?
The graveyard is full of them
“We do everything” reads as “best at nothing.” So we sequence: win the supplier-audit wedge in pharma, then carry the engine outward, ring by ring — when a real buyer pulls us in.
The current is with us: standards bodies are converging on a common ISO spine with vertical clause-packs — exactly the shape of an engine-plus-configuration architecture.
Built as an engine, not an app
The pipeline is fixed; standards, vocabulary and templates are configuration. Adding an industry is a pack, not a fork.
Core — today
Pharma & adjacent GxP
Supplier audit wedge, India Tier-2/3 manufacturers first. The pharma pack is proven; every artifact is regulator-grade.
Ring 1
Food & beverage, cosmetics, cell & gene
~75% engine reuse. HACCP / FSSC packs are configuration, not code.
Ring 2
Automotive, aerospace
IATF / AS9100 supplier-audit motion — the same primitive, new clause libraries.
Ring 3
Chemicals, energy, agri
Every standards-governed industry, entered only when a real buyer pulls us in.
See the work, not the brochure
Three of the fifteen modules, drawn from the real product.
Run the whole audit in one place
- Phase stepper from planning to e-signed closure certificate
- Evidence, findings and supplier responses on the audit itself
- At-risk filters so nothing stalls silently
Findings become CAPAs by themselves
- Auto-spawned CAPA with owner, due date and severity carried over
- Triage → RCA → actions → effectiveness check, each gate signed
- Cross-module trail intact — one thread from finding to closure
Suppliers answer without accounts
- Secure no-login links; sections assigned to the right person
- One inbox for the supplier QA head instead of 800 messages
- 12-dimension risk snapshot updates as responses land
“Make regulated-industry compliance reproducible, defensible, and affordable — so quality teams spend their day improving products, not chasing paper.”
No customer logos here yet — we're pre-launch, and we don't rent logos or invent quotes. We'd rather earn yours in 60 days.
Pharma today. Every regulated industry in time.
See the engine on the vertical that matters to you.