Regulatory compliance is stuck in the document age. Regulations are published as 200-page PDFs, interpreted by specialists who can't scale, and tracked in spreadsheets that are outdated the moment they're completed. CE marking alone requires mapping products to harmonized standards, assessing essential requirements, and maintaining declarations of conformity — for every product variant, every regulatory update, every market. Your compliance team spends 60–80% of its time on documentation and evidence gathering. The actual judgment takes minutes. Everything around it takes weeks.
Parse regulatory text into decision trees. Map directives to requirements, requirements to standards, standards to evidence criteria.
Deploy agents that traverse the decision logic against your operational data. Evidence generation, gap analysis, and compliance checks — automated.
Production deployment with regulatory update monitoring. When standards change, the system flags what's affected.
Weeks → hours per product variant
Structured the full CE marking conformity assessment workflow — applicability assessment, harmonized standards mapping, risk assessment (EN ISO 12100), technical documentation generation, and declaration of conformity. A new product variant processes through full conformity assessment in hours instead of weeks. Regulatory updates propagate automatically to affected products.
Your compliance team is a bottleneck for product launches or market entry
Regulatory changes require weeks of manual review and re-documentation
Audit preparation consumes an entire quarter every year
You're entering a new regulated market and need compliance infrastructure from scratch
Every compliance engagement includes the structured rulebase, agent deployment, operator training, and complete documentation of the regulatory logic. Your team maintains and extends it independently.
We'll tell you where the friction is, what should stay human, and whether automation is worth doing.