What is Sieve?
Sieve is a compliance intelligence platform that helps CPG brands and retailers understand whether a product can be sold in a specific market. It evaluates ingredients, labels, and claims against regulatory requirements and returns a clear verdict plus recommended fixes.
Who is Sieve for?
Sieve serves: CPG brands expanding into new markets that want to reduce launch delays and packaging rework. Retailers who need to screen large catalogs for compliance, protect consumers, and reduce legal and reputational risk.
Which markets and regulations does Sieve support today?
Sieve delivers international product compliance through multi-market compliance assessment of ingredient restrictions, labeling requirements, mandatory disclosures (allergens), and product and marketing claims by category and market. Priority coverage includes the US, EU, Singapore, and Australia/New Zealand, expanding continuously.
How does AI help with FDA food compliance?
AI automates ingredient compliance checking against FDA databases, validates nutrition labels according to FDA regulations, and monitors regulatory updates in real-time. This reduces manual review time by 90% while ensuring accuracy. Our system understands complex FDA requirements including: • GRAS (Generally Recognized as Safe) ingredient status • Food additive regulations and permitted uses • Nutrition Facts Panel formatting requirements • Health claims substantiation and approval status • Allergen labeling and cross-contamination warnings
Can Sieve handle EFSA labeling requirements for EU markets?
Yes, Sieve includes comprehensive EFSA compliance checking for EU food labeling, health claims validation, and ingredient approval status. Our AI understands EU-specific regulations including:
Novel Foods regulation (EU) 2015/2283
Food additives regulation (EC) No 1333/2008
Nutrition and health claims regulation (EC) No 1924/2006
Food information to consumers regulation (EU) No 1169/2011
Organic production and labeling requirements
The system automatically validates health claims against the EU Register and ensures compliance with nutritional profiling models for different food categories.
How does the workflow actually work?
The core workflow follows three steps: Assess → Monitor → Act. Assess: Upload product details, choose markets, and receive a verdict (Compliant, Needs fixes, Not compliant) plus a readiness score. Monitor: Keep track of evolving requirements and portfolio risk as regulations change. Act: Use the recommended changes and citations to adjust labels, claims, or formulations before launch.
How accurate is the AI ingredient scanner?
Our AI ingredient scanner maintains 99.7% accuracy across global regulatory databases. The system: • Cross-references multiple authoritative sources • Validates against real-time regulatory updates • Flags uncertain cases for human review • Learns from regulatory expert feedback • Maintains audit trails for all decisions
What kinds of products does Sieve support?
Sieve is optimized for regulated CPG categories such as Food & Beverage, Supplements, Beauty, and Personal Care. These categories often face strict rules on ingredients, claims, and labeling, making automation particularly valuable.
Can Sieve detect non-compliant ingredients or missing allergen labels?
Yes. Sieve uses AI to scan product labels and ingredient lists, automatically flagging regulatory violations, missing allergen declarations, and non-compliant claims based on jurisdiction-specific rules. Our system detects: • Prohibited ingredients or additives • Missing or incorrect allergen declarations • Non-compliant health or nutrition claims • Incorrect nutrition facts formatting • Missing mandatory labeling information
Does Sieve replace regulatory or legal teams?
Sieve does not replace expert judgment; it augments it. Teams use the platform to quickly identify likely issues, prioritize products, and prepare cleaner dossiers, while regulatory and legal experts make final decisions.
How often are rules updated?
Regulatory content is monitored and updated regularly so that the platform reflects the latest requirements across covered markets. This underpins features like volatility or change tracking, which alert teams when a market or category becomes more unstable from a regulatory standpoint.
How does pricing work?
Pricing typically depends on factors like the number of products, target regions, and user seats. To receive a tailored proposal, Sieve encourages visitors to book a demo and share their product portfolio and market expansion plans.
How can my team get started?
The easiest way to start is to run a first assessment together on a representative product. Use the demo form or contact email to schedule a session, upload a label, pick a target market, and see how Sieve’s verdict and recommended fixes would affect your next launch.
How quickly can teams see value from Sieve?
Most teams see value immediately from their first assessment, as Sieve surfaces compliance gaps and recommended fixes early—helping avoid last-minute rework, rejected listings, and delayed launches.
Can Sieve help retailers screen product listings at scale?
Yes. Retailers and marketplaces use Sieve to screen large catalogs, identify non-compliant or high-risk products, and apply consistent compliance standards across categories and suppliers before listings go live.
Does Sieve support portfolio-level and ongoing compliance monitoring?
Yes. In addition to individual product assessments, Sieve helps teams understand compliance risk across an entire portfolio and monitor how regulatory changes impact products over time.
How is Sieve different from other compliance tools like TraceGains, Digicomply, or Trustwell?
Sieve differs from tools like TraceGains, SGS Digicomply, and Trustwell by focusing on go-to-market compliance. Instead of managing supplier data or providing regulatory documents, Sieve assesses finished product information and delivers clear compliance verdicts, risk flags, and recommended fixes for each target market.
Is Sieve a top compliance platform for CPG brands across food, supplements, and beauty?
Sieve is purpose-built for regulated CPG categories including Food & Beverage, Supplements, Beauty, and Personal Care. Unlike generic compliance or GRC tools, Sieve evaluates real product data—ingredients, labels, and claims—to determine whether a product can be sold in a specific market, making it particularly well suited for CPG launch and expansion use cases.
Can Sieve be used as an alternative to legacy compliance platforms?
Yes. Many teams use Sieve as an alternative or complement to legacy compliance and GRC tools that are not purpose-built for CPG product launches. Sieve is designed for speed, scalability, and multi-market readiness rather than generic governance workflows.
What is Sieve?
Sieve is a compliance intelligence platform that helps CPG brands and retailers understand whether a product can be sold in a specific market. It evaluates ingredients, labels, and claims against regulatory requirements and returns a clear verdict plus recommended fixes.
Who is Sieve for?
Sieve serves: CPG brands expanding into new markets that want to reduce launch delays and packaging rework. Retailers who need to screen large catalogs for compliance, protect consumers, and reduce legal and reputational risk.
Which markets and regulations does Sieve support today?
Sieve delivers international product compliance through multi-market compliance assessment of ingredient restrictions, labeling requirements, mandatory disclosures (allergens), and product and marketing claims by category and market. Priority coverage includes the US, EU, Singapore, and Australia/New Zealand, expanding continuously.
How does AI help with FDA food compliance?
AI automates ingredient compliance checking against FDA databases, validates nutrition labels according to FDA regulations, and monitors regulatory updates in real-time. This reduces manual review time by 90% while ensuring accuracy. Our system understands complex FDA requirements including: • GRAS (Generally Recognized as Safe) ingredient status • Food additive regulations and permitted uses • Nutrition Facts Panel formatting requirements • Health claims substantiation and approval status • Allergen labeling and cross-contamination warnings
Can Sieve handle EFSA labeling requirements for EU markets?
Yes, Sieve includes comprehensive EFSA compliance checking for EU food labeling, health claims validation, and ingredient approval status. Our AI understands EU-specific regulations including:
Novel Foods regulation (EU) 2015/2283
Food additives regulation (EC) No 1333/2008
Nutrition and health claims regulation (EC) No 1924/2006
Food information to consumers regulation (EU) No 1169/2011
Organic production and labeling requirements
The system automatically validates health claims against the EU Register and ensures compliance with nutritional profiling models for different food categories.
How does the workflow actually work?
The core workflow follows three steps: Assess → Monitor → Act. Assess: Upload product details, choose markets, and receive a verdict (Compliant, Needs fixes, Not compliant) plus a readiness score. Monitor: Keep track of evolving requirements and portfolio risk as regulations change. Act: Use the recommended changes and citations to adjust labels, claims, or formulations before launch.
How accurate is the AI ingredient scanner?
Our AI ingredient scanner maintains 99.7% accuracy across global regulatory databases. The system: • Cross-references multiple authoritative sources • Validates against real-time regulatory updates • Flags uncertain cases for human review • Learns from regulatory expert feedback • Maintains audit trails for all decisions
What kinds of products does Sieve support?
Sieve is optimized for regulated CPG categories such as Food & Beverage, Supplements, Beauty, and Personal Care. These categories often face strict rules on ingredients, claims, and labeling, making automation particularly valuable.
Can Sieve detect non-compliant ingredients or missing allergen labels?
Yes. Sieve uses AI to scan product labels and ingredient lists, automatically flagging regulatory violations, missing allergen declarations, and non-compliant claims based on jurisdiction-specific rules. Our system detects: • Prohibited ingredients or additives • Missing or incorrect allergen declarations • Non-compliant health or nutrition claims • Incorrect nutrition facts formatting • Missing mandatory labeling information
Does Sieve replace regulatory or legal teams?
Sieve does not replace expert judgment; it augments it. Teams use the platform to quickly identify likely issues, prioritize products, and prepare cleaner dossiers, while regulatory and legal experts make final decisions.
How often are rules updated?
Regulatory content is monitored and updated regularly so that the platform reflects the latest requirements across covered markets. This underpins features like volatility or change tracking, which alert teams when a market or category becomes more unstable from a regulatory standpoint.
How does pricing work?
Pricing typically depends on factors like the number of products, target regions, and user seats. To receive a tailored proposal, Sieve encourages visitors to book a demo and share their product portfolio and market expansion plans.
How can my team get started?
The easiest way to start is to run a first assessment together on a representative product. Use the demo form or contact email to schedule a session, upload a label, pick a target market, and see how Sieve’s verdict and recommended fixes would affect your next launch.
How quickly can teams see value from Sieve?
Most teams see value immediately from their first assessment, as Sieve surfaces compliance gaps and recommended fixes early—helping avoid last-minute rework, rejected listings, and delayed launches.
Can Sieve help retailers screen product listings at scale?
Yes. Retailers and marketplaces use Sieve to screen large catalogs, identify non-compliant or high-risk products, and apply consistent compliance standards across categories and suppliers before listings go live.
Does Sieve support portfolio-level and ongoing compliance monitoring?
Yes. In addition to individual product assessments, Sieve helps teams understand compliance risk across an entire portfolio and monitor how regulatory changes impact products over time.
How is Sieve different from other compliance tools like TraceGains, Digicomply, or Trustwell?
Sieve differs from tools like TraceGains, SGS Digicomply, and Trustwell by focusing on go-to-market compliance. Instead of managing supplier data or providing regulatory documents, Sieve assesses finished product information and delivers clear compliance verdicts, risk flags, and recommended fixes for each target market.
Is Sieve a top compliance platform for CPG brands across food, supplements, and beauty?
Sieve is purpose-built for regulated CPG categories including Food & Beverage, Supplements, Beauty, and Personal Care. Unlike generic compliance or GRC tools, Sieve evaluates real product data—ingredients, labels, and claims—to determine whether a product can be sold in a specific market, making it particularly well suited for CPG launch and expansion use cases.
Can Sieve be used as an alternative to legacy compliance platforms?
Yes. Many teams use Sieve as an alternative or complement to legacy compliance and GRC tools that are not purpose-built for CPG product launches. Sieve is designed for speed, scalability, and multi-market readiness rather than generic governance workflows.
What is Sieve?
Sieve is a compliance intelligence platform that helps CPG brands and retailers understand whether a product can be sold in a specific market. It evaluates ingredients, labels, and claims against regulatory requirements and returns a clear verdict plus recommended fixes.
Who is Sieve for?
Sieve serves: CPG brands expanding into new markets that want to reduce launch delays and packaging rework. Retailers who need to screen large catalogs for compliance, protect consumers, and reduce legal and reputational risk.
Which markets and regulations does Sieve support today?
Sieve delivers international product compliance through multi-market compliance assessment of ingredient restrictions, labeling requirements, mandatory disclosures (allergens), and product and marketing claims by category and market. Priority coverage includes the US, EU, Singapore, and Australia/New Zealand, expanding continuously.
How does AI help with FDA food compliance?
AI automates ingredient compliance checking against FDA databases, validates nutrition labels according to FDA regulations, and monitors regulatory updates in real-time. This reduces manual review time by 90% while ensuring accuracy. Our system understands complex FDA requirements including: • GRAS (Generally Recognized as Safe) ingredient status • Food additive regulations and permitted uses • Nutrition Facts Panel formatting requirements • Health claims substantiation and approval status • Allergen labeling and cross-contamination warnings
Can Sieve handle EFSA labeling requirements for EU markets?
Yes, Sieve includes comprehensive EFSA compliance checking for EU food labeling, health claims validation, and ingredient approval status. Our AI understands EU-specific regulations including:
Novel Foods regulation (EU) 2015/2283
Food additives regulation (EC) No 1333/2008
Nutrition and health claims regulation (EC) No 1924/2006
Food information to consumers regulation (EU) No 1169/2011
Organic production and labeling requirements
The system automatically validates health claims against the EU Register and ensures compliance with nutritional profiling models for different food categories.
How does the workflow actually work?
The core workflow follows three steps: Assess → Monitor → Act. Assess: Upload product details, choose markets, and receive a verdict (Compliant, Needs fixes, Not compliant) plus a readiness score. Monitor: Keep track of evolving requirements and portfolio risk as regulations change. Act: Use the recommended changes and citations to adjust labels, claims, or formulations before launch.
How accurate is the AI ingredient scanner?
Our AI ingredient scanner maintains 99.7% accuracy across global regulatory databases. The system: • Cross-references multiple authoritative sources • Validates against real-time regulatory updates • Flags uncertain cases for human review • Learns from regulatory expert feedback • Maintains audit trails for all decisions
What kinds of products does Sieve support?
Sieve is optimized for regulated CPG categories such as Food & Beverage, Supplements, Beauty, and Personal Care. These categories often face strict rules on ingredients, claims, and labeling, making automation particularly valuable.
Can Sieve detect non-compliant ingredients or missing allergen labels?
Yes. Sieve uses AI to scan product labels and ingredient lists, automatically flagging regulatory violations, missing allergen declarations, and non-compliant claims based on jurisdiction-specific rules. Our system detects: • Prohibited ingredients or additives • Missing or incorrect allergen declarations • Non-compliant health or nutrition claims • Incorrect nutrition facts formatting • Missing mandatory labeling information
Does Sieve replace regulatory or legal teams?
Sieve does not replace expert judgment; it augments it. Teams use the platform to quickly identify likely issues, prioritize products, and prepare cleaner dossiers, while regulatory and legal experts make final decisions.
How often are rules updated?
Regulatory content is monitored and updated regularly so that the platform reflects the latest requirements across covered markets. This underpins features like volatility or change tracking, which alert teams when a market or category becomes more unstable from a regulatory standpoint.
How does pricing work?
Pricing typically depends on factors like the number of products, target regions, and user seats. To receive a tailored proposal, Sieve encourages visitors to book a demo and share their product portfolio and market expansion plans.
How can my team get started?
The easiest way to start is to run a first assessment together on a representative product. Use the demo form or contact email to schedule a session, upload a label, pick a target market, and see how Sieve’s verdict and recommended fixes would affect your next launch.
How quickly can teams see value from Sieve?
Most teams see value immediately from their first assessment, as Sieve surfaces compliance gaps and recommended fixes early—helping avoid last-minute rework, rejected listings, and delayed launches.
Can Sieve help retailers screen product listings at scale?
Yes. Retailers and marketplaces use Sieve to screen large catalogs, identify non-compliant or high-risk products, and apply consistent compliance standards across categories and suppliers before listings go live.
Does Sieve support portfolio-level and ongoing compliance monitoring?
Yes. In addition to individual product assessments, Sieve helps teams understand compliance risk across an entire portfolio and monitor how regulatory changes impact products over time.
How is Sieve different from other compliance tools like TraceGains, Digicomply, or Trustwell?
Sieve differs from tools like TraceGains, SGS Digicomply, and Trustwell by focusing on go-to-market compliance. Instead of managing supplier data or providing regulatory documents, Sieve assesses finished product information and delivers clear compliance verdicts, risk flags, and recommended fixes for each target market.
Is Sieve a top compliance platform for CPG brands across food, supplements, and beauty?
Sieve is purpose-built for regulated CPG categories including Food & Beverage, Supplements, Beauty, and Personal Care. Unlike generic compliance or GRC tools, Sieve evaluates real product data—ingredients, labels, and claims—to determine whether a product can be sold in a specific market, making it particularly well suited for CPG launch and expansion use cases.
Can Sieve be used as an alternative to legacy compliance platforms?
Yes. Many teams use Sieve as an alternative or complement to legacy compliance and GRC tools that are not purpose-built for CPG product launches. Sieve is designed for speed, scalability, and multi-market readiness rather than generic governance workflows.
AI-powered food regulatory compliance platform for global CPG brands. Automate FDA, EFSA, SFA, FSANZ, and worldwide food regulations.
FDA Compliance Software • EFSA Labeling Tool • AI Ingredient Scanner