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Home » Topics » Regulatory Watch

Regulatory Watch
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Salt

FDA to Amend Standards of Identity to Include Salt Substitutes

The FDA aims to give food manufacturers the flexibility to reduce sodium content in standardized foods in alignment with the agency’s public health goals.
May 6, 2025

The FDA aims to give food manufacturers the flexibility to reduce sodium content in standardized foods in alignment with the agency’s public health goals.


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food ingredients
Regulatory Update

What’s Ahead for the GRAS Pathway?

The self-affirmed "generally recognized as safe" status may be subject to upcoming regulatory changes.
Sam Jockel
Sam Jockel
Ashley Yull
Ashley Yull
April 14, 2025

Self-affirmed GRAS determinations made by the food industry are being called into question at federal and state levels, even without health or safety concerns associated with substances that are designated as GRAS.


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Spoonful of peanut butter on peanut butter jar

FDA Issues Draft Guidance on Sanitation for Low-Moisture, Ready-to-Eat Foods

This guidance provides the agency’s current thinking on establishing a routine sanitation program for low-moisture, ready-to-eat foods that can help prevent pathogen contamination events and also sets forth recommendations for corrective actions.
April 11, 2025

This guidance provides the agency’s current thinking on establishing a routine sanitation program for low-moisture, ready-to-eat foods that can help prevent pathogen contamination events and also sets forth recommendations for corrective actions.


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produce on display in a grocery store
Track and Trace

Are You Ready for FSMA’s Section 204(d) Food Traceability Rule?

FDA’s FSMA Section 204(d) rule requires traceability for critical high-spoilage foods, which have been known to carry foodborne illnesses. If you’re not prepared for the new rule, your competition will be.
Wayne Labs, Senior Contributing Technical Editor
Wayne Labs
March 19, 2025

FDA’s FSMA Section 204(d) rule requires traceability for critical high-spoilage foods, which have been known to carry foodborne illnesses. If you’re not prepared for the new rule, your competition will be.



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Plate of food

FDA Issues Draft Guidance on Labeling Plant-Based Alternatives to Animal-Derived Foods

The FDA’s draft guidance includes plant-based alternatives to eggs, seafood, poultry, meat and dairy products (excluding plant-based milk alternatives) that fall under FDA jurisdiction.
March 4, 2025

The FDA’s draft guidance includes plant-based alternatives to eggs, seafood, poultry, meat and dairy products (excluding plant-based milk alternatives) that fall under FDA jurisdiction.


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Baby food

FDA Issues Guidance on Lead Action Levels for Processed Baby Food

FDA considers the following action levels to be achievable by the food industry when control measures are taken to minimize the presence of lead.
February 4, 2025

FDA considers the following action levels to be achievable by the food industry when control measures are taken to minimize the presence of lead.


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Container ship at port

FSIS to Consider Additional Import Inspection Establishment Applications

January 8, 2025

FSIS will consider, on a case-by-case basis, GOIs for official import inspection establishments outside the 50-mile geographic radius of a U.S. land or sea port of entry.


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A woman looking into a grocery store cooler

FDA Finalizes Updated 'Healthy' Nutrient Content Claim

December 20, 2024

Manufacturers who choose to use the “healthy” claim have three years to conform but can use the new criteria sooner. 


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USDA FSIS LOGO

FSIS to Consider Additional Import Inspection Establishment Applications

December 16, 2024

FSIS will consider, on a case-by-case basis, GOIs for official import inspection establishments outside the 50-mile geographic radius of a U.S. land or sea port of entry.


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Qualified Importer Program

Guidance for the Voluntary Qualified Importer Program Updated

The FDA is implementing a revised inspection approach, strategically designed to optimize program efficiency by leveraging other oversight activities, which may reduce user fees.
December 2, 2024

The FDA is implementing a revised inspection approach, strategically designed to optimize program efficiency by leveraging other oversight activities, which may reduce user fees.


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