Inlet is an end-to-end compliance platform that spans multiple regulated industries. Each module is purpose-built for its vertical — same powerful engine, tailored regulatory intelligence.
Full lifecycle compliance for beauty, personal care, and skincare products
From INCI list validation to market submission dossiers. Inlet covers the entire regulatory lifecycle for cosmetics products across 9 global markets — EU, US, UK, Canada, ASEAN, Japan, South Korea, Malaysia, and Singapore.
Validate a formulation against all target markets before investing in production. Catch banned ingredients, concentration violations, and missing warnings in seconds.
Take an existing product approved in the EU and check compliance for US, ASEAN, and Japan simultaneously. Get a gap analysis with specific remediation steps.
When you swap an ingredient, instantly see which markets are affected and what new restrictions apply. No manual cross-referencing.
Additive, labeling, allergen, and safety compliance for food products
From food additives and GRAS substances to allergen declarations and nutrition labeling. Inlet covers the full regulatory landscape for food and beverage products — including additives, flavorings, health claims, and labeling requirements across major markets.
Validate a food formulation against additive regulations, allergen requirements, and labeling rules across all target markets before going to production.
Upload a product label and check it against mandatory labeling elements — ingredient lists, allergen callouts, nutrition panels, health claims — for every target market.
Take a product approved for the US market and check what changes are needed for EU, UK, Canada, and Japan. Get a market-by-market gap analysis.
Classification, registration, and post-market compliance for medical devices
From device classification to technical documentation and post-market surveillance. Inlet will cover the full medical device regulatory lifecycle — including EU MDR, FDA 510(k), UK UKCA marking, and Health Canada MDEL across major markets.
Determine the regulatory class of your device across EU, US, and other markets. Get a clear pathway to market with required documentation and timelines.
Identify predicate devices, generate substantial equivalence arguments, and build the complete 510(k) submission package with automated document generation.
Migrate existing MDD-certified devices to EU MDR. Get a gap analysis against the new GSPR requirements and a remediation roadmap.
Every vertical benefits from the same core platform infrastructure.
Deterministic rules, conditional logic, and Navi AI — consistent architecture across all verticals.
Ask regulatory questions in natural language. Navi cites specific regulations and explains edge cases.
US, EU, UK, Canada, ASEAN, Malaysia, Singapore, Japan, South Korea — each with local regulatory databases.
Auto-generate submission-ready documents tailored to each market's format and requirements.
Real-time compliance rates, market readiness scores, regulatory alerts, and activity feeds.
194 endpoints and Model Context Protocol. Integrate compliance into any workflow or AI agent.
We're building the compliance infrastructure layer for every regulated industry.
Start with cosmetics or food & beverage today. Add modules as your business expands into new verticals.