Accelerate time to market

Accelerate time to market

with AI-assisted compliance

with AI-assisted compliance

Signify automates compliance for manufacturers by analyzing documents to ensure regulatory requirements are met throughout the product life cycle.

Signify automates compliance for manufacturers by analyzing documents to ensure regulatory requirements are met throughout the product life cycle.

Signify AI automates compliance for manufacturers by analyzing documents

Deploy AI to automate compliance and gain a strategic advantage

Reduce review times by up to 90%, and focus on growth with our AI-driven compliance command center.

Supplier Verification

Quality & Safety

Labeling and Exports

Verify your suppliers comply with the standards and regulations that impact your operation. Boost confidence in selecting reliable and ethical suppliers.

Deploy AI to automate compliance and gain a strategic advantage

Reduce review times by up to 90%, and focus on growth with our AI-driven compliance command center.

Ensure compliance with import regulations and fair trade laws, simplifying your process and increasing confidence in your supplier choices.

Deploy AI to automate compliance and gain a strategic advantage

Reduce review times by up to 90%, and focus on growth with our AI-driven compliance command center.

Quality & Safety

Supplier Verification

Labeling and Exports

Verify your suppliers comply with the standards and regulations that impact your operation. Boost confidence in selecting reliable and ethical suppliers.

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.

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.

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

With Signify, you ensure every step across the product life cycle conforms to applicable regulatory requirements and standards. Our AI-powered workflow enables you to tackle complex regulatory reviews with confidence.

Eliminate uncertainty from compliance

With Signify, you ensure every step across the product life cycle conforms to applicable regulatory requirements and standards. Our AI-powered workflow enables you to tackle complex regulatory reviews with confidence.

Eliminate uncertainty from compliance

With Signify, you ensure every step across the product life cycle conforms to applicable regulatory requirements and standards. Our AI-powered workflow enables you to tackle complex regulatory reviews with confidence.

Always-on Compliance Monitoring

Signify automatically reviews documents to uncover compliance risks in real-time without the need for manual gap analysis and conformity assessments.

Always-on Compliance Monitoring

Signify automatically reviews documents to uncover compliance risks in real-time without the need for manual gap analysis and conformity assessments.

Always-on Compliance Monitoring

Signify automatically reviews documents to uncover compliance risks in real-time without the need for manual gap analysis and conformity assessments.

Choose Framework

Select from thousands of available frameworks to test compliance with standards, regulations, laws, contracts, and more.

Choose Framework

Select from thousands of available frameworks to test compliance with standards, regulations, laws, contracts, and more.

Choose Framework

Select from thousands of available frameworks to test compliance with standards, regulations, laws, contracts, and more.

Upload Documentation

Bring your documentation, including labels, policies, SOPs, controls, and technical specs, to find potential nonconformity issues.

End data errors

With Scale, say goodbye to inconsistent reporting and SLAs from multiple systems. Trust in one streamlined process and point of contact for each country.

Upload Documentation

Bring your documentation, including labels, policies, SOPs, controls, and technical specs, to find potential nonconformity issues.

Continuous Monitoring

Signify automatically detects changes in regulations and your documents. Get real-time conformity analysis at all times.

Continuous Monitoring

Signify automatically detects changes in regulations and your documents. Get real-time conformity analysis at all times.

Continuous Monitoring

Signify automatically detects changes in regulations and your documents. Get real-time conformity analysis at all times.

Demonstrate Compliance

Share an audit trail and traceability matrix with regulators, auditors, and notified bodies from your compliance command center.

Demonstrate Compliance

Scale makes global payroll management a breeze, from visa support to handling PTO and expenses.

Demonstrate Compliance

Scale makes global payroll management a breeze, from visa support to handling PTO and expenses.

Easy, accurate, regulatory compliance

Easy, accurate, regulatory compliance

Trust and security first

Enterprise-grade software ensures your data is secure with encryption in-transit and at rest. We offer private cloud deployments and adhere to NIST and OWASP standards. SOC2 certification is in progress.

Trust and security first

Enterprise-grade software ensures your data is secure with encryption in-transit and at rest. We offer private cloud deployments and adhere to NIST and OWASP standards. SOC2 certification is in progress.

Trust and security first

Enterprise-grade software ensures your data is secure with encryption in-transit and at rest. We offer private cloud deployments and adhere to NIST and OWASP standards. SOC2 certification is in progress.

Specialized agents

Specialized agents

Specialized agents

Who is Signify for?

Who is Signify for?

Who is Signify for?

Thousands of frameworks

Review and test compliance across thousands of laws, regulatory frameworks, and standards in one place.

Thousands of frameworks

Review and test compliance across thousands of laws, regulatory frameworks, and standards in one place.

Thousands of frameworks

Review and test compliance across thousands of laws, regulatory frameworks, and standards in one place.

  • 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.

  • 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.

  • 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.

  • 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.

  • 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.

  • 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.

Updates from Signify

From new product launches to exciting company updates, stay up-to-date with the latest Signify news.

Updates from Signify

From new product launches to exciting company updates, stay up-to-date with the latest Signify news.

Compliance automation FAQ

Compliance automation FAQ

Do you use my company's data to train Signify AI models?

We would only do so for customers who ask us to build bespoke models for internal-use agents. Other than that, we will never train a model with your data.

Do you use my company's data to train Signify AI models?

We would only do so for customers who ask us to build bespoke models for internal-use agents. Other than that, we will never train a model with your data.

Do you use my company's data to train Signify AI models?

We would only do so for customers who ask us to build bespoke models for internal-use agents. Other than that, we will never train a model with your data.

How long does the implementation take?

How long does the implementation take?

How long does the implementation take?

Can I create custom assesments?

Can I create custom assesments?

Can I create custom assesments?

Is the AI making decisions on my behalf?

Is the AI making decisions on my behalf?

Is the AI making decisions on my behalf?