Health Canada released a new modification to the List of Permitted Supplemental Ingredients that expands when and how caffeine can be used
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On September 4, 2025, Health Canada released Version 4.0 of the Good Manufacturing Practices (GMP) Guide for Natural Health Products
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Medical device shortage reporting requirements have recently changed, and it is essential for manufacturers and importers to stay informed.
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Health Canada has released a draft guidance document on co-packaged drug products, now open for public consultation. The guidance explains
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Starting March 2025, Health Canada requires all cosmetic notifications to include a Canadian Agent. Learn what this means for your business.
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As of March 12, 2025 Health Canada has implemented changes to the Cannabis Act and its Regulations. These changes may
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Stay compliant with the latest Health Canada FOP labelling updates affecting fresh coconut and breakfast cereals. Learn key policy changes here.
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The Natural and Non-prescription Health Products Directorate (NNHPD) has changed the review process for Class III Natural Health Product (NHP)
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Are Your Supplemental Ingredients Compliant? Canada’s New Rules Explained If your business sells supplemented foods in Canada, major regulatory updates
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Introduction Health Canada’s new front-of-package label rules are set to take effect on January 1, 2026, marking a significant shift
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Understanding ‘Made in Canada’ Claims With trade tensions rising and new tariffs affecting cross-border business, Canadian brands must ensure they
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As a Canadian medical device license (MDL) holder, you are subject to an annual license renewal procedure. The renewal process
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Have you ever looked at a food label and wondered why all that information is there? Labels do more than
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