Streamline your path to compliance—with AI
Purpose-built AI compliance agents for consumer product manufacturers—speeding approvals, minimizing risk, and unlocking scalable growth across CPG and durables.
Operationalize compliance with AI agents and scale smarter
Reduce review cycles by up to 90%—AI agents manage the regulatory burden so your teams can drive product velocity and growth.
Artwork Validation
GMP Documentation
Supplier Verification
Analyze artwork, packaging, and labels against regulatory requirements—identifying compliance gaps before they reach the market and cause costly recalls.
Spend less time on compliance review tasks
Manual compliance can’t compete with Signify. Reduce compliance reviews from weeks to hours with higher accuracy to eliminate the risk of errors and omissions.
Eliminate uncertainty from compliance
Signify’s AI compliance agents oversee every stage of the product life cycle—navigating regulatory requirements, streamlining reviews, and reducing risk at scale.
Autonomous Compliance Agents
Signify’s AI agents work around the clock—automatically detecting risks, surfacing gaps, and ensuring regulatory alignment without manual review.
Upload Documentation
Bring your documentation, including labels, policies, SOPs, controls, and technical specs, to find potential nonconformity issues.
Identify Requirements
The compliance agent will select the applicable requirements from thousands of available frameworks.
Compliance Checks
Your Compliance AI agent will automatically perform conformity assessments, build traceability matrices, and identify top risks.
Demonstrate Compliance
Share an audit trail and traceability matrix with regulators, auditors, and notified bodies from your compliance command center.
AI compliance agents FAQs
What is Signify, and how does it help CPG companies manage product compliance?
Signify deploys purpose-built AI compliance agents to support mid-market and enterprise CPG companies. These agents streamline regulatory processes across food & beverage, cosmetics, dietary supplements, and OTC drugs—cutting review times by up to 90% and enabling faster, more efficient delivery of compliant, high-quality products.
How does Signify protect sensitive regulatory and product data?
Can Signify integrate with existing ERP, eQMS, or PLM software?
Is customization available within Signify to match our specific compliance needs?
Does Signify's AI automate compliance decision-making?
What is the typical implementation timeline for Signify in mid-market or enterprise CPG companies?
Global Regulatory Intelligence, Agent-Powered
Signify’s AI agents operate with built-in expertise across thousands of international laws and frameworks—ensuring every compliance review meets the highest global standards.
OSHA
Assure safe and healthy working conditions.
Tax and Trade Bureau
Regulates and collects taxes on trade and imports of alcohol and tobacco.
Federal Aviation Administration
Regulates civil aviation in the United States and surrounding international waters.
U.S. Dairy Export Council
Represents the global trade interests of U.S. dairy producers.
ISO 13485
Quality management system for the design and manufacture of medical devices.
EU MDR
Clinical investigation and sale of medical devices for human use.
FDA CFR Title 21
Published by the U.S. Food and Drug Administration (FDA) governing food and drugs in the United States.
GS1
Standards for barcodes and the corresponding issue company prefixes.
ITAR
Controls the export and import of defense-related articles and services
OSHA
Assure safe and healthy working conditions.
Tax and Trade Bureau
Regulates and collects taxes on trade and imports of alcohol and tobacco.
Federal Aviation Administration
Regulates civil aviation in the United States and surrounding international waters.
U.S. Dairy Export Council
Represents the global trade interests of U.S. dairy producers.
ISO 13485
Quality management system for the design and manufacture of medical devices.
EU MDR
Clinical investigation and sale of medical devices for human use.
FDA CFR Title 21
Published by the U.S. Food and Drug Administration (FDA) governing food and drugs in the United States.
GS1
Standards for barcodes and the corresponding issue company prefixes.
ITAR
Controls the export and import of defense-related articles and services
OSHA
Assure safe and healthy working conditions.
Tax and Trade Bureau
Regulates and collects taxes on trade and imports of alcohol and tobacco.
Federal Aviation Administration
Regulates civil aviation in the United States and surrounding international waters.
U.S. Dairy Export Council
Represents the global trade interests of U.S. dairy producers.
ISO 13485
Quality management system for the design and manufacture of medical devices.
EU MDR
Clinical investigation and sale of medical devices for human use.
FDA CFR Title 21
Published by the U.S. Food and Drug Administration (FDA) governing food and drugs in the United States.
GS1
Standards for barcodes and the corresponding issue company prefixes.
ITAR
Controls the export and import of defense-related articles and services
Tax and Trade Bureau
Regulates and collects taxes on trade and imports of alcohol and tobacco.
OSHA
Assure safe and healthy working conditions.
EU MDR
Clinical investigation and sale of medical devices for human use.
Federal Aviation Administration
Regulates civil aviation in the United States and surrounding international waters.
ISO 13485
Quality management system for the design and manufacture of medical devices.
ITAR
Controls the export and import of defense-related articles and services
FDA CFR Title 21
Published by the U.S. Food and Drug Administration (FDA) governing food and drugs in the United States.
GS1
Standards for barcodes and the corresponding issue company prefixes.
IEC 62304
Requirements for the life cycle processes of medical device software.
U.S. Dairy Export Council
Represents the global trade interests of U.S. dairy producers.
Tax and Trade Bureau
Regulates and collects taxes on trade and imports of alcohol and tobacco.
OSHA
Assure safe and healthy working conditions.
EU MDR
Clinical investigation and sale of medical devices for human use.
Federal Aviation Administration
Regulates civil aviation in the United States and surrounding international waters.
ISO 13485
Quality management system for the design and manufacture of medical devices.
ITAR
Controls the export and import of defense-related articles and services
FDA CFR Title 21
Published by the U.S. Food and Drug Administration (FDA) governing food and drugs in the United States.
GS1
Standards for barcodes and the corresponding issue company prefixes.
IEC 62304
Requirements for the life cycle processes of medical device software.
U.S. Dairy Export Council
Represents the global trade interests of U.S. dairy producers.
Tax and Trade Bureau
Regulates and collects taxes on trade and imports of alcohol and tobacco.
OSHA
Assure safe and healthy working conditions.
EU MDR
Clinical investigation and sale of medical devices for human use.
Federal Aviation Administration
Regulates civil aviation in the United States and surrounding international waters.
ISO 13485
Quality management system for the design and manufacture of medical devices.
ITAR
Controls the export and import of defense-related articles and services
FDA CFR Title 21
Published by the U.S. Food and Drug Administration (FDA) governing food and drugs in the United States.
GS1
Standards for barcodes and the corresponding issue company prefixes.
IEC 62304
Requirements for the life cycle processes of medical device software.
U.S. Dairy Export Council
Represents the global trade interests of U.S. dairy producers.
GS1
Standards for barcodes and the corresponding issue company prefixes.
Tax and Trade Bureau
Regulates and collects taxes on trade and imports of alcohol and tobacco.
OSHA
Assure safe and healthy working conditions.
ITAR
Controls the export and import of defense-related articles and services
Federal Aviation Administration
Regulates civil aviation in the United States and surrounding international waters.
ISO 13485
Quality management system for the design and manufacture of medical devices.
EU MDR
Clinical investigation and sale of medical devices for human use.
FDA CFR Title 21
Published by the U.S. Food and Drug Administration (FDA) governing food and drugs in the United States.
IEC 62304
Requirements for the life cycle processes of medical device software.
U.S. Dairy Export Council
Represents the global trade interests of U.S. dairy producers.
GS1
Standards for barcodes and the corresponding issue company prefixes.
Tax and Trade Bureau
Regulates and collects taxes on trade and imports of alcohol and tobacco.
OSHA
Assure safe and healthy working conditions.
ITAR
Controls the export and import of defense-related articles and services
Federal Aviation Administration
Regulates civil aviation in the United States and surrounding international waters.
ISO 13485
Quality management system for the design and manufacture of medical devices.
EU MDR
Clinical investigation and sale of medical devices for human use.
FDA CFR Title 21
Published by the U.S. Food and Drug Administration (FDA) governing food and drugs in the United States.
IEC 62304
Requirements for the life cycle processes of medical device software.
U.S. Dairy Export Council
Represents the global trade interests of U.S. dairy producers.
GS1
Standards for barcodes and the corresponding issue company prefixes.
Tax and Trade Bureau
Regulates and collects taxes on trade and imports of alcohol and tobacco.
OSHA
Assure safe and healthy working conditions.
ITAR
Controls the export and import of defense-related articles and services
Federal Aviation Administration
Regulates civil aviation in the United States and surrounding international waters.
ISO 13485
Quality management system for the design and manufacture of medical devices.
EU MDR
Clinical investigation and sale of medical devices for human use.
FDA CFR Title 21
Published by the U.S. Food and Drug Administration (FDA) governing food and drugs in the United States.
IEC 62304
Requirements for the life cycle processes of medical device software.
U.S. Dairy Export Council
Represents the global trade interests of U.S. dairy producers.
Updates from Signify
From new product launches to exciting company updates, stay up-to-date with the latest Signify news.
Compliance AI Agents
for consumer products
Signify helps regulatory and product compliance teams in CPG and durables manufacturing launch products faster by automating global compliance.
Signify is the leading compliance system for consumer products—leveraging AI agents to automate gap analysis, streamline conformity checks, and accelerate safe, high-quality product launches.
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