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22

Aug 2025

FDA Color Additive Petition: What Red 3 Bans Mean for Ingredient Companies
FDA Color Additive Petition: What Red 3 Bans Mean for Ingredient Companies
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Background On January 15, 2025, the FDA revoked authorization for FD&C Red No. 3 (erythrosine) for use in foods, including dietary supplements, and in ingested drugs. The agency followed a […] Read More >>

06

Jun 2025

FDA’s AI Rollout: What Elsa and CDRH-GPT Mean for Regulatory Submissions in the U.S.
FDA’s AI Rollout: What Elsa and CDRH-GPT Mean for Regulatory Submissions in the U.S.
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On June 2, 2025, the U.S. Food and Drug Administration (FDA) officially launched Elsa, a generative AI tool designed to assist FDA staff with core functions such as reviewing clinical […] Read More >>

14

Nov 2024

What Safety Data is Required for a GRAS or NDI
What Safety Data is Required for a GRAS or NDI
By
A Generally Recognized as Safe (GRAS) or New Dietary Ingredient (NDI) notification is essential for novel food ingredient manufacturers and distributors to ensure that their product is recognized as safe […] Read More >>

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