FDA

The GRAS Act: Transforming United States’ Food Safety Landscape
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On August 12, 2025, Representative Frank Pallone (D-NJ) introduced the Grocery Reform and Safety Act...
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GRAS Procedure: Looking to the Future while Anchored in the Past
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What’s a GRAS Procedure?  The Generally Recognized as Safe (GRAS) procedure is a regulatory framework...
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FDA Issues Draft Guidance on AI in Drugs and Devices
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FDA Releases Draft Guidance on AI in Drug and Medical Device Development The U.S. Food...
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Understanding Health Claims: FDA Authorization and Qualification
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Health claims on food labels play a critical role in informing consumers about the relationship...
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The Commercialization of Medical Devices in Europe and the USA: Similarities and Differences
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The American Market Among the motivations that could drive a medical device manufacturer to commercialize...
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Regulatory Challenges of New Foods: EU and US Perspective
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Navigating the world of food innovation can be exciting but also a bit tricky, especially...
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Labelling of Cosmetic Products in the United States
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In the United States, cosmetic products must comply with specific labeling requirements mandated by the...
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Milestones of Food Supplements’ Marketing Procedure: EU and US in Comparison
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The global food supplement market has been experiencing steady growth for the last few years....
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USA Food Safety: GRAS Notice vs Self-Affirmed
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In the world of food safety and regulation, the process of introducing new ingredients into...
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Panoramica sul nuovo regolamento cosmetico USA
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Cos’è il MoCRA? MoCRA è l’acronimo di Modernization of Cosmetic Regulation Act. Questo atto era...
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