Compliance today is Risky
AI-native Food Assurance Platform
Supplier PFAS. FSMA 204 Traceability. EU EmpCo Directive. Substance Phase-Out. State Additive Labels.
And 180+ more compliance work - executed by Mergen AI agents with global regulatory knowledge coverage.
of compliance teams still manually track regulatory changes.
average cost of a single FDA product recall.
FDA food recalls in 2025 preventable with automated compliance intelligence.
180+ compliance workflows across the F&B value chain
Screen suppliers for PFAS contamination risk and ensure compliance with emerging restrictions.
Establish end-to-end traceability records required under FDA FSMA Rule 204.
Assess and comply with EU Emissions Compliance Directive requirements across your supply chain.
Track and manage the phase-out of restricted substances from your product formulations.
Generate state-specific additive labeling that meets varying US state regulations.
Generate compliant label versions for every target jurisdiction in one workflow.
Verify if an ingredient is permitted in your target market before development begins.
Compile jurisdiction-specific export dossiers with all required certificates and declarations.
Build a hazard analysis and critical control point plan grounded in regulatory requirements.
Validate that a product formulation meets all regulatory limits for additives and contaminants.
Classify recall severity and determine affected product scope within minutes.
Assess how new or amended regulations affect your existing product portfolio.
Generate jurisdiction-specific nutrition facts panels from product composition data.
Identify compliance gaps before an audit with a structured readiness check.
Screen and qualify new suppliers against regulatory and food safety requirements.
Validate allergen declarations against per-jurisdiction formatting and disclosure rules.
Determine whether an ingredient requires novel food or GRAS approval in each market.
Determine whether a product can be legally exported to a specific market.
Monitor real-time compliance status across your entire product portfolio.
Validate nutrition claims against jurisdiction-specific thresholds and requirements.
Verify supplier CoAs against specifications and regulatory thresholds.
Automatically triage new regulatory updates and flag what matters to your portfolio.
Evaluate the regulatory impact of swapping one ingredient for another.
Execute a structured audit against GFSI-benchmarked food safety standards.
Assess whether a health claim is approvable in your target jurisdictions.
Verify Foreign Supplier Verification Program compliance for imported products.
Visualize compliance risk across products, markets, and regulatory domains.
Review final label artwork against all applicable regulatory requirements before printing.
Trace contamination or non-compliance back to its source through the supply chain.
Develop preventive controls plans for FSMA compliance including hazard analysis.
Build and maintain allergen control plans aligned with regulatory requirements.
Investigate border rejections and generate corrective action plans.
Analyze competitor product labels and claims to benchmark your compliance positioning.
Verify clean label, natural, and free-from claims against regulatory definitions per market.
Assess compliance gaps across multiple client portfolios for consulting engagements.
Screen suppliers for PFAS contamination risk and ensure compliance with emerging restrictions.
Establish end-to-end traceability records required under FDA FSMA Rule 204.
Assess and comply with EU Emissions Compliance Directive requirements across your supply chain.
Track and manage the phase-out of restricted substances from your product formulations.
Generate state-specific additive labeling that meets varying US state regulations.
Generate compliant label versions for every target jurisdiction in one workflow.
Verify if an ingredient is permitted in your target market before development begins.
Compile jurisdiction-specific export dossiers with all required certificates and declarations.
Build a hazard analysis and critical control point plan grounded in regulatory requirements.
Validate that a product formulation meets all regulatory limits for additives and contaminants.
Classify recall severity and determine affected product scope within minutes.
Assess how new or amended regulations affect your existing product portfolio.
Generate jurisdiction-specific nutrition facts panels from product composition data.
Identify compliance gaps before an audit with a structured readiness check.
Screen and qualify new suppliers against regulatory and food safety requirements.
Validate allergen declarations against per-jurisdiction formatting and disclosure rules.
Determine whether an ingredient requires novel food or GRAS approval in each market.
Determine whether a product can be legally exported to a specific market.
Monitor real-time compliance status across your entire product portfolio.
Validate nutrition claims against jurisdiction-specific thresholds and requirements.
Verify supplier CoAs against specifications and regulatory thresholds.
Automatically triage new regulatory updates and flag what matters to your portfolio.
Evaluate the regulatory impact of swapping one ingredient for another.
Execute a structured audit against GFSI-benchmarked food safety standards.
Assess whether a health claim is approvable in your target jurisdictions.
Verify Foreign Supplier Verification Program compliance for imported products.
Visualize compliance risk across products, markets, and regulatory domains.
Review final label artwork against all applicable regulatory requirements before printing.
Trace contamination or non-compliance back to its source through the supply chain.
Develop preventive controls plans for FSMA compliance including hazard analysis.
Build and maintain allergen control plans aligned with regulatory requirements.
Investigate border rejections and generate corrective action plans.
Analyze competitor product labels and claims to benchmark your compliance positioning.
Verify clean label, natural, and free-from claims against regulatory definitions per market.
Assess compliance gaps across multiple client portfolios for consulting engagements.
The Three Pillars of Compliance AI
Everything Compliance Needs, One AI Platform
Most tools handle one piece of compliance. Mergen AI covers the full stack - from the knowledge you need, to the work that gets done. Three pillars, one platform, zero gaps.
Knowledge
Your business data and documents combined with Mergen AI’s global regulatory knowledge - one unified foundation for every compliance decision.
Exploration
AI agents that search across your data, regulatory rules, and the open internet - so you get answers, not more reading.
Automation
Hand off compliance tasks to AI agents that do the work end-to-end. 180+ ready-made workflows you can customize to fit how your team operates.
Why Mergen AI
What Makes Mergen AI Different
Not another compliance chatbot. Mergen AI is an execution platform - built to do the work, not just describe it.
Execution, Not Advice
AI agents fill regulatory forms, generate required documents, and produce submission-ready dossiers. Most tools advise. Mergen AI executes.
Compliance Context Graph
Every execution, approval, and rationale feeds into a persistent Compliance Context Graph - linking products, regulations, evidence, and agent actions. Full traceability.
Automation That Compounds
Each execution becomes structured precedent. Over time, one-off compliance work becomes repeatable automation - eliminating re-learning and continuously improving.
Global Coverage, One System
Global regulatory knowledge - FDA, EU, APAC, Latin America - unified into one structured knowledge infrastructure. One source of truth.
10× Faster Compliance
What took months now takes days. Automated validation, form generation, and real-time compliance checks eliminate coordination bottlenecks.
Human-in-the-Loop by Design
Regulatory teams review and approve before work begins, then evaluate every output. Scientific judgment stays with your team. Automation handles the rest.
Compliance tools tell you what to do. Mergen AI does it.
Who It's For
Built for the Entire F&B Value Chain
Whether you produce, import, export, distribute, sell, or advise - if compliance is part of your F&B business, Mergen AI is built for you.
Manufacturers
Ingredient validation, label compliance, product registration, GMP audits, HACCP plans, and reformulation assessments. AI agents handle execution across global jurisdictions.
- Regulatory Affairs Manager
- QA Director
- Food Safety Manager
- Labeling Specialist
Importers
Import permits, foreign product registration, customs documentation, and FSVP compliance. Automated with per-jurisdiction regulatory knowledge.
- Import Compliance Officer
- Regulatory Affairs Specialist
Exporters
Target market regulatory mapping, export documentation, certificates of origin, and label adaptation for destination markets.
- Export Compliance Officer
- International Regulatory Affairs Manager
Distributors
Portfolio compliance monitoring, recall tracking, supplier documentation verification, and regulatory deadline management across your entire catalog.
- Compliance Monitoring Analyst
- Portfolio Compliance Manager
Retailers & Private Label
Supplier compliance verification, label review, allergen management, and front-of-pack nutrition labeling for every product on your shelves.
- Private Label Compliance Manager
- Supplier Quality Auditor
Consultants & Advisors
Multi-client compliance management, regulatory research, dossier preparation, and audit support. Multiply your team's output with AI agents.
- Regulatory Consultant
- Compliance Advisory Lead
Pricing
Start free. Scale when ready.
No feature gating - every plan includes every agent and workflow. You only choose how much you use.
Free
$0forever
Explore the Platform
Pro
$39/month
For Individual Professionals
Team
$125/month
5 Users, 5x Pro Limits
Enterprise: dedicated or sovereign deployments · details on the pricing page
From the blog
Insights from real compliance work
Regulatory change, labelling, suppliers and food safety, written by the Mergen AI team.

/5 min read
The Whey Switch: How a Dairy Tariff Fight Lands on Your Label
Tariffs and a US whey ban are forcing fast supplier switches. Here’s what that can break on your label.

/6 min read
The Changeover Gap: What the Gatorade Dye Recall Teaches Every Label Team
PepsiCo promised natural colours, then recalled 122,021 cases for undeclared synthetic dyes. What went wrong, and how to avoid it in your own phase-out.

/7 min read
AB 418 Marks the Start of a New Compliance Model
From static standards to continuous, state-specific execution.
Get Started Today
Ready to Put AI to Work on Compliance?
Start with a free 14-day exploration or book a demo with our team. See how Mergen AI transforms compliance from a bottleneck into a competitive advantage.
No credit card required · Full platform access · 14-day free exploration
Contact
Get in Touch
Book a demo, request a consultation, or ask a question. We respond within 24 hours.
Contact Information
- Address
Schwartz Reisman Innovation Campus
108 College Street
Toronto, ON M5G 1L6, Canada
- hello@mergenai.ca
- Phone
- +1 (647) 939-7034
