FY 2025 OMUFA Fees Due June 2: What You Need to Know
The FDA has confirmed that FY 2025 OMUFA facility fees are due soon. If your business was registered as a
... Read moreThe FDA has confirmed that FY 2025 OMUFA facility fees are due soon. If your business was registered as a
... Read moreThe FDA has just announced a significant decision: Red No. 3, a widely used synthetic dye in foods and ingested
... Read moreIf you’re thinking about bringing a pharmaceutical product to the Canadian market, getting familiar with drug submission pathways is a
... Read moreIn the pharmaceutical industry, proper drug submission management is crucial to the success of any drug development process. The submission
... Read moreOverview Manufacturers of prescription and non-prescription drugs are required to obtain a Drug Identification Number (DIN) before the drug product
... Read more1. What are over-the-counter drug products (OTC drugs)? Non-prescription drugs also called over-the-counter (OTC drugs), are health products that can
... Read moreAdvertising is something almost all people experience and view daily. Yet, it can be challenging to navigate this space as
... Read moreCOVID-19 and Hard Surface Disinfectants – What You Need to Know In Canada, chemical products that are used to clean,
... Read moreThe 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
... Read moreAll drugs subject to the Food and Drug Regulations are required to gain premarket authorization prior to issuance of a
... Read moreWhen Health Canada authorizes a drug to be marketed in Canada, a Drug Identification Number (DIN) is issued to the
... Read moreThe label and package are the first points of interaction between a health product and a consumer. Prior to the
... Read moreBACKGROUND Originally implemented in 1920 after the inception of the Federal department of Health in 1919, the Food and Drugs
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