“A sweater is like life, you get nothing out of it
that you don’t put into it!”
– Marilyn Monroe
As autumn settles in, transformation is everywhere. The air feels crisp, the light turns golden, and a sense of focus takes hold. This season marks a natural time for reflection, refinement, and renewed energy to finish the year strong.
Across all divisions, our team is embracing this momentum. From regulatory initiatives to creative campaigns and clinical innovation, collaboration continues to drive everything we do. We are refining our strategies, strengthening partnerships, and preparing for an exciting conclusion to 2025.
So pour yourself a warm drink and take a moment to explore what’s new at SNI. This season’s updates, insights, and ideas are designed to inspire growth and carry your business confidently into the year ahead.
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- BULLETIN: FOP Labelling
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NHP Clinical Trials: Feasibility and Portfolio Assessment
Clinical trials for natural health products (NHPs) and cosmetics bring science to the forefront of beauty and wellness. Whether evaluating a vitamin formulation, an herbal remedy, or a rejuvenating cream, these studies add evidence-based rigour to traditional claims and consumer expectations. Across the world, sponsors are shifting from isolated tests to strategic research programs designed to validate both safety and efficacy.
If you are considering your next clinical trial or deciding which to prioritize, a feasibility and portfolio assessment can help identify which studies are most likely to produce meaningful and beneficial results. A well-structured research plan helps ensure that each study is built on sound science, robust design, and reliable methodology - keeping your innovation grounded in evidence.
» Learn more about feasibility and portfolio assessment in our latest blog
Health Canada's Recent Update to the GMPs for NHPs
One of the most important aspects of selling Natural Health Products (NHPs) in Canada or dietary supplements in the United States is staying compliant with Good Manufacturing Practices (GMPs). Recently, Health Canada introduced updates to the GMP requirements for NHPs, raising the bar for quality, safety, and consistency across the industry.
As fall settles in, it is the perfect time for manufacturers to take a closer look at their operations, which involves ensuring that every process, record, and facility meets current standards. Strong GMP compliance not only protects consumers but also reinforces trust in your brand, helping your products stand out in a competitive market.
» Learn about these the recent changes in our blog
New & Upcoming FDA Changes
On September 4, 2025, the U.S. Food and Drug Administration (FDA) unveiled its Unified Regulatory Agenda, outlining several important updates to food and dietary supplement oversight. Three key initiatives are drawing attention across the industry: a proposed rule to mandate GRAS (Generally Recognized As Safe) notifications, a final front-of-package (FOP) nutrition labelling rule, and a reclassification proposal for a previously excluded dietary supplement ingredient.
These developments highlight a continued shift toward greater transparency and accountability within the U.S. regulatory landscape. For manufacturers and brand owners, staying informed and proactive will be essential. From formulation to labelling, now is the time to review internal processes, align with evolving standards, and ensure compliance as new expectations take shape.
» Learn what they mean for your business and how to stay ahead of the curve
Canadian Regulations for Red Light Therapy Devices
Red light therapy devices are gaining major attention in the beauty and wellness world, becoming a staple in modern skincare routines. As demand continues to rise, these products have also drawn the attention of Health Canada.
In Canada, most red light therapy devices are classified as medical devices and must comply with the Medical Device Regulations. This includes specific requirements for product licensing, as well as both pre-market and post-market obligations. When compliance and innovation align, the result is not only effective but also transformative for both consumers and manufacturers.
» Learn more about red light therapy device regulations in our blog
Canadian GMPs for Cosmetics
Good Manufacturing Practices (GMP) for cosmetics in Canada form the foundation of every safe and high-quality product. Under the Cosmetic Regulations, Health Canada requires manufacturers to maintain strict standards for production, documentation, and quality control.
Understanding and implementing these requirements before entering the market helps prevent costly issues and ensures that products meet regulatory expectations once they reach consumers.
Canadian Regulations for VHPs (Pet Supplements)
If you are looking to sell pet supplements in Canada, it is important to have a strong compliance plan in place. From notifying Health Canada about your product to ensuring accurate bilingual labelling and meeting importation requirements, every detail matters. Missing even one step can delay market entry or create compliance challenges down the road.
This guide explains the licensing requirements for pet supplements in Canada and outlines how to set your products up for success. When it comes to compliance, precision and preparation are the key ingredients for building consumer trust and maintaining long-term market access.
Bilingual Labelling and Exemptions for Foods
Bilingual labelling is one of the fundamental requirements for selling products in Canada. Both federal and provincial regulations mandate that product labels appear in English and French to ensure accessibility and compliance across the country.
There are, however, a few exceptions. Certain foods may be exempt from bilingual labelling, such as specialty products with religious or ceremonial significance, local foods sold exclusively within a small community, or test products with temporary authorizations. While the rules are strict, understanding the available exemptions can help businesses navigate Canada’s labelling landscape with confidence.
» Read more about the bilingual labelling exemptions for food products here
FRONT-OF-PACK DEADLINE APPROACHING
In case you haven't heard, your pre-packaged food product requires an update!
DEADLINE: January 1, 2026
We've outlined some of the requirements, exemptions and details exclusively for our readers.
Understanding the new Front-of-Package (FOP) Nutrition Label Requirements.
Front-of-package (FOP) labelling refers to the placement of a clear and standardized nutrition symbol on the front of prepackaged food products. In Canada, this symbol appears when a product is considered high in one or more of the following nutrients: saturated fat, sugars, or sodium.
New Update to Health Canada's Interim Policy on Front-of-Package Labelling
Health Canada released interim policy statements that address Front-of-Package (FOP) nutrition labelling for two specific categories of food: prepackaged fresh coconut and ready-to-eat breakfast cereals.
» These updates may have broader implications beyond just the FOP label, learn more here
Front-of-Package (FOP) Labelling: Understanding Exemptions
Products that are fully exempt are never required to carry a FOP symbol, regardless of their nutritional content or usage. There are also conditional exemptions apply only if specific conditions are met.
» In this post, we clarify qualifying conditions and fully exempt products
Navigating Health Canada’s FOP labelling regulations can be complex, but we make it simple.
Our team provides end-to-end regulatory support, from ensuring compliance with FOP and NFt requirements to designing packaging that meets legal standards while standing out on shelves.
Whether you need guidance on regulatory changes, NFt alignment, or government approvals, we streamline the process so you can focus on your business. Let us handle the details—reach out today for expert support in FOP labelling, food labelling compliance, and regulatory-friendly design!
CONTACT US
SNI knows the ins and outs of the regulations for all consumer products. Contact us today (regulatory@sourcenutra.com) and let us help you make the regulations work for your products.
Whatever your regulatory, packaging and/or clinical research needs are- contact SNI today to learn how we can help you achieve brand success and market penetration in 2025 (info@sourcenutra.com).
SNI is your “one-stop-solution” for strategic consulting, regulatory compliance, clinical trials, graphic design, bilingual labelling and importation and fulfillment services for foods, natural health products, cosmetics, medical devices and pharmaceutical products.
Contact us today to learn more about how we can help you get your products to market quickly, compliantly and cost effectively.
