FDA - SNI Inc.

26 Feb 2026

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

FoodFDA, FDA inspections, food chemical safety, food regulatory compliance, front of package labeling, GRAS reform, Human Foods Program, Regulatory Affairs, U.S. food law

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…

24 Feb 2026

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

Foodclean label claims, color additives, enforcement discretion, FDA, food labeling compliance, food reformulation, natural food colors, petroleum based dyes, Regulatory Affairs, U.S. food regulations

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…

22 Jan 2026

Health Canada vs. FDA: Regulatory Frameworks and Compliance

General RegulationsFDA, FDA vs Health Canada Regulations, health canada, regulatory frameworks

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.…

16 Sep 2025

New and Upcoming FDA Changes in 2025: GRAS Rules, FOP Labelling, and Supplement Ingredients – What You Need to Know

FDAcanadian regulations, cross-border compliance, dietary supplements, DSHEA, FDA, FDA Unified Agenda, food labelling, FOP labelling, front-of-package labelling, GRAS, health canada, ingredient safety, NHP, nicotinamide mononucleotide, NMN, novel foods, Nutrition Labelling, Regulatory Affairs, self-affirmed GRAS, U.S. regulations

On September 4, 2025, the U.S. Food and Drug Administration (FDA) published its Unified Regulatory Agenda, a key planning document that outlines the Agency’s top priorities over the coming year. Among the many proposed and final rules, three initiatives stand out for their potential to significantly impact food and dietary…

24 Mar 2025

FDA ESG NextGen Launch: Key Dates, Features, and Transition Guide for Users

FDAESG NextGen, FDA, NetGen, Regulatory Update, US Regulations

As part of its ongoing efforts to modernize and streamline the submission process, the FDA is transitioning from its legacy Electronic Submission Gateway (ESG) system to ESG NextGen. This new platform is designed to make regulatory submissions more efficient, secure, and user-friendly, all while enhancing the overall user experience. The…

15 May 2024

Allergen Labelling & Recalls – What you need to know

UncategorizedAllergic reactions, Canadian Food Inspection Agency (CFIA), CFIA, Customer Safety, FDA, Food Allergies, food labelling, Food Recall, food safety, Lactose Intolerance, Recall, risk evaluation, US FDA

According to Food Allergy Canada, more than 3 million Canadians self-report having at least one food allergy and 1-in-2 Canadian households are impacted by food allergy. Accurate food labelling is crucial to make sure consumers get the required information about the product they are about to eat! What’s the risk?…

10 Apr 2024

Get to Know SNI: Clinical Research Services

UncategorizedAnti-aging, antioxidants, Bioactives, Cardiovascular Studies, Clinical Research, Clinical trials, Comparator Studies, consumer product testing, Cosmetic testing, CT, Diabetes Studies, Efficacy, FDA, Haircare, health canada, Immunology, Irritation Studies, Marketing Studies, Microbiome, Moisturization, natural health products, NHP, NHPs, Observational Studies, Performance Studies, pharmaceutical, Pharmaceutical Studies, Phase I Studies, Phase II Studies, Phase III Studies, Phase IV Studies, Prebiotics, Probiotics, Safety, skincare, SNI, sunscreen

At SNI, we have built a robust team of clinical trials professionals, all dedicated to the success of your project. Together, they bring over 250+ years of experience in clinical, regulatory, and medicine and have completed 850+ clinical trials combined. A key benefit to sponsors is our diverse experience across…

13 Mar 2024

How to Tell If a Supplement Is Legitimate

UncategorizedCFIA, dietary supplement, FDA, food industry, food labelling, food supply, health, ingredient quality, nutrients, regulations, supplement safety, supplements

In today's health-conscious world, supplements have become increasingly popular. Whether you're looking to boost your energy levels, improve your immune system, or support your overall well-being, the supplement market offers a plethora of options. However, with so many products available, it can be challenging to determine which ones are legitimate…

08 Mar 2024

March is Nutrition Month in Canada

UncategorizedCanada's Healthy Eating Strategy, Canadian Food Inspection Agency, CFIA, Dietitians, Dietitians Canada, FDA, food industry, food labelling, food supply, health, Health and Fitness, ingredient quality, nutrients, Nutrition month, nutrition month in canada

March is Canadian Nutrition Month, an opportunity to acknowledge the importance of health and nutrition in our population. This initiative is spearheaded by Dietitians of Canada, an organization that continually recognizes the influence that dietitians have on Canadian’s well-being. A registered dietitian can guide you in adapting your lifestyle and diet…

11 Jan 2024

5 Dietary Supplement Violations and How to Avoid Them

UncategorizedBatch Production Records, Consumer health risk, Dietary Supplement Health and Education Act, dietary supplements, DSHEA, False advertising, FDA, FDA warning letters, GMP, Good Manufacturing Practices, The Food and Drug Administration, US dietary supplements

With a projected U.S. market size of over $300 billion by 2030, the dietary supplement category has never presented more opportunities for brand success. In a health-conscious society, dietary supplements can play a significant role in supporting individuals' well-being, but the growing popularity of these supplements has brought attention to the…