
Health Canada Fees 2026: Updates for Devices, Drugs & Cannabis
Health Canada has updated its fees effective April 1, 2026, with changes applying across multiple regulated sectors, including medical devices,
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Health Canada has updated its fees effective April 1, 2026, with changes applying across multiple regulated sectors, including medical devices,
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The FDA has confirmed that FY 2025 OMUFA facility fees are due soon. If your business was registered as a
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If you’re thinking about bringing a pharmaceutical product to the Canadian market, getting familiar with drug submission pathways is a
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In the pharmaceutical industry, proper drug submission management is crucial to the success of any drug development process. The submission
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Overview Manufacturers of prescription and non-prescription drugs are required to obtain a Drug Identification Number (DIN) before the drug product
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1. What are over-the-counter drug products (OTC drugs)? Non-prescription drugs also called over-the-counter (OTC drugs), are health products that can
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Advertising is something almost all people experience and view daily. Yet, it can be challenging to navigate this space as
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COVID-19 and Hard Surface Disinfectants – What You Need to Know In Canada, chemical products that are used to clean,
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The Protecting Canadians from Unsafe Drugs Act (Vanessa’s Law) introduces amendments to the Food and Drugs Act that will improve Health Canada’s ability to
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All drugs subject to the Food and Drug Regulations are required to gain premarket authorization prior to issuance of a
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When Health Canada authorizes a drug to be marketed in Canada, a Drug Identification Number (DIN) is issued to the
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The label and package are the first points of interaction between a health product and a consumer. Prior to the
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BACKGROUND Originally implemented in 1920 after the inception of the Federal department of Health in 1919, the Food and Drugs
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