Introducing a new food ingredient into the Australian or New Zealand market means working within a regulatory system that takes safety seriously. FSANZ reviews novel
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Building your safety narrative for a GRAS notice begins with toxicological studies for GRAS conclusion, and this foundation is one of the most important parts of proving
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Health Canada has officially postponed the implementation of its proposed NHP cost recovery fees, which were initially expected to take effect on December 1, 2025.
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When it comes to importing human food and animal food into Canada, many businesses assume the process is similar. In reality, while both categories are
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Getting an NPN for sports supplements is essential for businesses looking to market their products legally in Canada. The Natural Product Number (NPN) is a
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If your company manufactures, repacks, relabels, or imports drugs for distribution in the U.S., it’s time to prepare for the FDA drug establishment renewal season.
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When exporting food supplements to Canada, understanding trade agreements can make a huge difference in your profitability. The Comprehensive Economic and Trade Agreement (CETA) between
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When it comes to ingredient safety, an expert panel plays one of the most critical roles in the GRAS (Generally Recognized as Safe) process. These
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Getting GRAS status for an enzyme is one of the most important steps to ensure your ingredient is recognized as safe for its intended use.
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Introduction: Why EFSA Novel Food Clinical Studies Matter Bringing a novel food to the European market requires more than innovation. It requires scientific proof of
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If you’re planning to introduce an innovative ingredient or food product in the European Union, understanding how to submit an EFSA novel food application is
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After years of uncertainty and legal disputes, the U.S. Food and Drug Administration (FDA) declared on September 29, 2025, that Beta Nicotinamide Mononucleotide (NMN) can
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