What to Know Before Submitting a GRAS Notice to the FDA
Thinking about launching a new food ingredient in the U.S. often raises an important question: how do you demonstrate safety to the
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January 21, 2026
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[blog_list]
What GRAS Really Means for Food and Ingredient Companies
If you manufacture or sell food ingredients in the United States, you have almost certainly come across the term GRAS. Yet many companies
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January 20, 2026
A Practical Guide to a Successful NDIN Submission
Introduction Bringing a new dietary ingredient to the U.S. market involves more than formulation and sourcing. If an ingredient does
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January 5, 2026
How Combining Ingredients For A GRAS Conclusion Affects Product Safety
Introduction When working toward a GRAS conclusion for an ingredient, a common question is whether it is possible to combine
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December 2, 2025
Expert Panel in GRAS Determinations: Why It Matters for Ingredient Safety
When it comes to ingredient safety, an expert panel plays one of the most critical roles in the GRAS (Generally
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October 16, 2025
Best Practices for Achieving GRAS Status for Manufacturers
Reaching GRAS status is an important step if you want your Generally Recognized as Safe ingredient accepted for use in
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September 23, 2025
The 7 Key Sections of a GRAS Dossier Every Business Should Understand
Preparing a GRAS dossier is one of the most important steps when seeking FDA recognition for a new substance in
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September 22, 2025
FDA Launches Real Time Adverse Event Reporting Dashboard for Cosmetic Products
The FDA adverse event reporting dashboard for cosmetic products is now live, offering businesses and consumers real time access to
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September 18, 2025
What the New FDA PreCheck Program Means for Drug Manufacturers
Introduction Announced on August 7, 2025, the FDA PreCheck program is a new initiative aimed at strengthening the domestic pharmaceutical
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August 13, 2025
FDA Proposes Compliance Extension And Releases New Tools For Food Traceability
The FDA food traceability rule is once again in the spotlight. On August 6, 2025, the U.S. Food and Drug
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August 7, 2025
FDA approves gardenia blue as Red No. 3 faces phase-out
The U.S. Food and Drug Administration (FDA) has approved gardenia blue, a plant-derived color additive, for limited use in certain
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July 18, 2025
FDA to Extend Food Traceability Rule: What You Need to Know
The FDA Food Traceability Rule compliance date could soon be pushed back. The U.S. Food and Drug Administration (FDA) is
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March 22, 2025
FDA to Revoke Use of Red No. 3: What You Need to Know
The FDA has just announced a significant decision: Red No. 3, a widely used synthetic dye in foods and ingested
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January 17, 2025
What’s Behind the FDA’s New Front-of-Package Labeling Proposal?
The FDA’s proposed front-of-package (FOP) nutrition labeling rule introduces significant changes to how nutritional information is displayed. This proposal reflects
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January 16, 2025
Understanding the FDA’s Updated “Healthy” Nutrient Content Claim
The FDA has finalized its updated definition for the “Healthy” nutrient content claim, aiming to promote better transparency in food
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January 11, 2025
FDA Sets 2028 Compliance Date for Food Labels
The U.S. Food and Drug Administration (FDA) recently announced a uniform compliance date for food labeling regulations. This update establishes
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January 10, 2025
How Drug Registration Works in the U.S. and What NDC Numbers Mean
Drug registration and NDC number might sound technical, but they play a big role in how medications make it to
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October 4, 2023
What you should know about FDA Approvals for Drugs & Medical Devices
Introduction: FDA approvals can be a complex process, but understanding its important steps can give you insight into how drugs
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March 27, 2023
How to Achieve GRAS Status for Your Ingredient
If you want to know how to get your ingredient generally recognized as safe (GRAS) by the FDA, you are
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February 12, 2023