The GRAS Process Under the Final Rule (Part 2): Increased Emphasis on Exposure

The finalized GRAS rule and associated Federal Register Notice1 emphasizes the FDA’s opinion that dietary…

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The Strictest Regulation on Infant Formula in Chinese History: How does it compare to the U.S. registration process?

On June 6th 2016, the China Food and Drug Administration (CFDA) published the final rule…

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New Draft Guidance on Allergy Assessment of Genetically Modified Plants from EFSA: More Tests to Ensure Safety for Everyone

The European Food Safety Authority (EFSA) has issued a new draft guidance on allergenicity testing…

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SupplySide West Speaking Engagement Teaser: Regulatory and Labeling Challenges of Natural Colors in the Era of ‘Clean Labels’

Synthetic coloring agents used in foods have periodically come under fire for having potentially adverse…

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Dietary Supplements in the U.S. and Abroad: Similarities and Differences

Demand for dietary and nutritional supplements worldwide continues to increase, with steady growth in the…

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The GRAS Process and Notifying FDA under the Final Rule (Part 1)

What makes for a successful Generally Recognized as Safe (GRAS) determination?  In the recent past…

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