For Regulatory & Compliance Teams

From weeks of manual review to auditable compliance in hours

You know the pain: tracking IFRA amendments, cross-referencing FEMA GRAS lists, maintaining allergen declarations across 12 markets. Aromis automates the lookup while keeping you in control of every decision.

10
compliance checkpoints
20+
regulatory frameworks
64K+
ingredients with real IDs
70%
target time reduction
Compliance Pipeline — 10-Checkpoint Sequential Gate Model
FORMULATION INPUTIngredients + ConcentrationsREGULATORY CONTEXTTarget Markets + FrameworksAPPLICATION PROFILEProduct Type + Packaging + StorageSEQUENTIAL COMPLIANCE PIPELINECP1Reg StatusCP2Conc LimitsCP3AllergensCP4CLP/GHSCP5RestrictedCP6LabellingCP7StabilityCP8Cross-ContCP9Doc CheckCP10Market ClearHUMAN REVIEW & APPROVAL GATE✓ APPROVE✗ REJECT↻ REQUEST REVISIONRe-enter pipelineMARKET CLEAREDCompliance Report · TDS · SDSEvidence Package · Audit TrailREJECTEDRejection Reason · Failed CheckpointsMandatory Comment · LoggedAUDIT TRAILEvery decision immutably loggedTimestamp · User · Evidence · Outcome

Automated Regulatory Lookup

Live
Instant validation against FEMA GRAS, EU 1334/2008, JECFA, IFRA
Real CAS numbers matched to regulatory status per jurisdiction
Concentration limit checks against application-specific thresholds
Restricted substance screening across all target markets
Allergen identification and declaration generation

Human Review, Not Replacement

Live
AI generates the assessment — you make the decision
Confidence indicators on every AI-generated output
Override capability with mandatory justification logging
Three-state review: Approve, Reject, Request Revision
Escalation paths for edge-case regulatory questions

Audit-Ready Evidence

Live
Every checkpoint generates exportable evidence
Full decision lineage — trace any output to its source data
Version history with diff tracking on reformulations
Immutable audit log — no retroactive edits
Bulk export for regulatory submissions and inspections

Multi-Market Clearance

Live
Run compliance across EU, US, APAC, LATAM simultaneously
Market-specific labelling requirement generation
CLP/GHS classification with H/P-statement assignment
Cross-contamination risk assessment for shared facilities
Documentation completeness verification per market
Before Aromis
Manual IFRA/FEMA/JECFA cross-referencing per ingredient
Spreadsheet-based allergen tracking across markets
Weeks to assess a reformulation for new markets
Evidence assembled ad-hoc before audits
Institutional knowledge lost when team members leave
With Aromis
Automated validation against 20+ frameworks in seconds
Allergen declarations generated per market automatically
Same-day compliance assessment on reformulations
Audit evidence always current, always exportable
Regulatory knowledge codified in the platform permanently

See a compliance run on a real formulation

We'll walk through the 10-checkpoint pipeline with your regulatory frameworks and market requirements.

Book Compliance DemoDownload Compliance Brief