FDA Human Foods Program 2026 Priority Deliverables: What Food Manufacturers Should Prepare For 

FDA Human Foods Program 2026 Priority Deliverables: What Food Manufacturers Should Prepare For 

The U.S. Food and Drug Administration has released its Human Foods Program 2026 Priority Deliverables, outlining the agency’s operational and regulatory focus areas for the coming year. While these deliverables do not create immediate new legal requirements, they provide a clear signal of where enforcement emphasis, rulemaking, and policy development are headed in…
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FDA Takes New Approach to “No Artificial Colors” Claims: What U.S. Food Manufacturers Need to Know in 2026 

FDA Takes New Approach to “No Artificial Colors” Claims: What U.S. Food Manufacturers Need to Know in 2026 

On February 5, 2026, the U.S. Food and Drug Administration announced a shift in how it will approach voluntary “no artificial colors” claims on food labels. The agency also granted two petitions expanding the availability of alternative colour additives derived from natural sources.  For manufacturers operating in the United States, this development…
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Health Canada NHP Site Licence Renewal Process and Requirements 

Health Canada NHP Site Licence Renewal Process and Requirements 

All Natural Health Product (NHP) site licence holders in Canada must renew their licence in accordance with the Natural Health Products Regulations. Although the renewal term varies by licence and is assigned directly by Health Canada, the obligation remains consistent across all sites: confirm continued compliance with Part 3 Good Manufacturing Practices (GMP) and keep Health…
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Food or Natural Health Product (NHP)? A Practical Guide to Classification and Compliance  

Food or Natural Health Product (NHP)? A Practical Guide to Classification and Compliance  

If you manufacture or import functional foods, fortified beverages, gummies, probiotics, botanicals, powders, or “wellness” products, you have likely run into the Canadian classification question: is this a food or a natural health product (NHP)?  In Canada, that decision is not exclusively linked to marketing preference. It is a regulatory classification that drives your allowed claims, label…
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Permitted vs. Not Permitted Pet Food Claims in Canada 

Permitted vs. Not Permitted Pet Food Claims in Canada 

Pet food claims in Canada follow a structured regulatory framework that ensures all statements on packaging, websites, and marketing materials are truthful, evidence based, and not misleading. Oversight is shared by the Competition Bureau, Canadian Food Inspection Agency (CFIA), and Health Canada, each of which plays a different role in evaluating…
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Health Canada Publishes 19 Updated NHP Monographs

Health Canada Publishes 19 Updated NHP Monographs

Health Canada’s Natural and Non-prescription Health Products Directorate (NNHPD) has officially published 19 updated Natural Health Product (NHP) monographs as part of the January 30, 2026 load. These updates affect a wide range of botanical ingredients, amino acids, and commonly used actives across the Canadian NHP market. For regulatory teams,…
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Foundations of OOS Investigations for Natural Health Products (NHPs) in Canada 

Foundations of OOS Investigations for Natural Health Products (NHPs) in Canada 

Unexpected laboratory results are an unavoidable reality in natural health products (NHPs) manufacturing. A potency value that does not match historical performance, a microbial result that sits uncomfortably close to its limit, or a chromatographic profile that looks unfamiliar can all signal that something requires closer attention. These results do not automatically…
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Nicotine Buccal Pouches in Canada: Health Canada’s Amendment Clarifies Prescription vs. Non Prescription Status

Nicotine Buccal Pouches in Canada: Health Canada’s Amendment Clarifies Prescription vs. Non Prescription Status

Health Canada has officially updated the Prescription Drug List to clarify the non prescription status of nicotine buccal pouches containing 4 milligrams of nicotine or less per dosage unit. This change provides long awaited clarity for manufacturers, importers, and retailers entering the rapidly growing nicotine pouch category. The amendment, effective…
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Health Canada vs. FDA: Regulatory Frameworks and Compliance 

Health Canada vs. FDA: Regulatory Frameworks and Compliance 

Regulatory compliance in Canada requires adherence to federal, provincial, and, in some cases, municipal legislation governing the safety, quality, and labelling of products placed on the Canadian market. Health Canada administers the regulation of a broad range of products primarily under the Food and Drugs Act and its associated Food and Drug Regulations.…
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Creative Design for Regulated Products: Why It Is Different and Why It Matters 

Creative Design for Regulated Products: Why It Is Different and Why It Matters 

If you have ever worked on a regulated product launch and assumed that packaging would be a relatively straightforward final step, the complexity likely became apparent very quickly. In regulated prepackaged consumer product categories, packaging is not a decorative layer added at the end of development. It is a regulated…
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