FDA confirms NMN is lawful in dietary supplements after industry pressure. Learn what this means for your business and compliance strategy.
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Learn how to meet FDA’s new dietary ingredient notification requirements for dietary supplements with new educational tools.
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Learn how to navigate the FDA approval process for shilajit in 5 simple steps. Follow our expert guide for a smoother regulatory journey.
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As a business owner operating in dietary supplements and health products, you are undoubtedly aware of the ever-evolving regulatory
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https://youtu.be/MlufAYFqQ1s In dietary supplements, navigating the intricate regulatory landscape is a challenging yet indispensable aspect of launching your product. Submitting
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Learn how to legally sell dietary supplements in the U.S. by following FDA regulations, labeling requirements, and ingredient safety standards. Stay compliant and grow your business.
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In today’s competitive marketplace, selling products on Amazon has become a lucrative opportunity for many entrepreneurs and businesses. However, navigating
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Consumers rely on Health Canada monographs to ensure the safety and efficacy of their products. But have you ever wondered
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As more and more people become health-conscious, the demand for supplements has skyrocketed. One of the most popular supplements on
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Navigating the complexities of the regulatory requirements for dietary supplements can be daunting. However, by understanding the framework, you can
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As a business owner, keeping up with regulatory requirements is a top priority. One such requirement is the FDA’s renewal
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Introduction: The FDA offers an online dietary supplement labeling guide that provides labeling requirements for supplement manufacturers. The guide covers
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Learn the key differences between GRAS vs NDI and how to choose the right FDA pathway for your ingredient. Stay compliant with expert insights.
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Background on FDA NAC Warning Letters: Navigating the FDA’s NAC system can be overwhelming. Understanding FDA warning letters is key
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Say you have a new ingredient and are ready to enter the US food market. To ensure this ingredient is
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Introduction Dietary supplements in the USA are very similar to natural health products (NHP regulations) in Canada and many products
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The U.S. Food and Drug Administration (FDA) has communicated via Letter of Enforcement Discretion that it will not oppose or
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On November 24, 2021, The Food and Drug Administration (FDA) sent correspondence to industry requesting information on the past use
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On October 13, 2021, the U.S. Food and Drug Administration (FDA) issued final guidance for the food industry that provides
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