Be aware that Health Canada is actively testing “Performance Supplements” on the market. Implementation of a quality program in accordance with GMP is the only way to ensure product integrity and avoid enforcement actions. Read More >>
Only health products that Health Canada authorizes for sale in Canada may be advertised. Thankfully, specific requirements exist for advertisements of prescription drugs to consumers for the best interest of […] Read More >>
What are Clinical Trials? Clinical trials are a type of biomedical research that is conducted to help doctors and researchers learn more about health, diseases, and effective treatments in order […] Read More >>
One of Health Canada’s largest initiatives in the past few years has been the Self-Care Framework, which implements a different approach to regulating products, that are purchased and applied directly […] Read More >>
Health claims are integral to the success of Natural Health Products (NHPs) here in Canada. They provide products with a competitive edge in the marketplace and consumers with the information […] Read More >>
Health Canada has recently announced the initiation of the Stop Illegal Marketing of Drugs and Devices (SIM-DD) program. Health Canada’s introduction of this particular program is part of its contribution […] Read More >>
The Safe Food for Canadians Regulations (SFCR) handbook was recently published to help businesses understand the requirements and the implications they may have. Now that 2019 is just around the […] Read More >>
Last summer, Health Canada implemented the Plain Language Labelling criteria for non-prescription products and has mandated that by June 30, 2021, all products must be compliant at the retail level. […] Read More >>
Service(s) related to this article: Low Risk Veterinary Health Product On August 10th, 2017, Health Canada sent an email notice to all stakeholders involved in the LRVHP Interim Notification […] Read More >>
Service(s) related to this article: Food Label & Claims, Food & Beverages, Product & Label Development Canada’s Food Guide is getting a makeover, and Health Canada is expected to […] Read More >>
In November 2013, Health Canada’s Food Directorate received an application for a therapeutic claim about eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA) and triglyceride lowering. The information below is a summary […] Read More >>
We have received notice that the Natural and Non-prescription Health Products Directorate (NNHPD) will initiate a new policy with respect to post-licence audit failures. The NNHPD implemented a new […] Read More >>
The Food Directorate of Health Canada has released a report “Summary of Health Canada’s Assessment of Health Claim about Vegetables and Fruit and Heart Disease”. The report discusses the consumption […] Read More >>
Big Changes Around the Corner for All Foods in Canada Safe Foods for Canadians Regulations and Licensing Requirements The most significant change in the history of Canadian Food and Drug […] Read More >>
Reprinted from Functional Ingredients Many are already aware of Canada’s much more stringent and cumbersome regulatory model for supplements (called Natural Health Products, or NHPs, in Canada). Every product needs […] Read More >>
NHPD has released a revised Compendium of Monographs Guidance Document. This document is open for comment until October 26, 2013. The NHPD has issued a revision to its Compendium of […] Read More >>
CFIAs food labelling modernization process has been proposed to align with Safe Food for Canadians Act and reduce red tape for industry. CFIA has proposed to introduce a new food […] Read More >>
On May 1, 2013 the CFIA announced that they will no longer be conducting food label reviews, as part of their mandatory pre-market registration, for certain meat and processed products. […] Read More >>
Some food-like NHPs were granted Temporary Marketing Authorizations with novel foods or food additives that have not yet been approved by Health Canada. It is the Food Directorate’s expectation that […] Read More >>
March 26, 2013: dicentra conducted its first webinar of 2013. Critical American and Canadian updates including FDA’s proposed rules to amend cGMPs for food facilities under FSMA, the FDA’s Draft […] Read More >>
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