 Health Canada Hand Sanitizer Registration Temporary expedited approval for non-compliant products Health Canada took the decision on Wednesday the 18th of March to allow temporary access to hand sanitizers, disinfectants that don’t fully meet standard regulatory requirements. This measure is due to the shortage of these products during the COVID-19 pandemic. In […]
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FDA hand sanitizer registration US FDA sets temporary regulations for alcohol-based Hand Sanitizer Because of the actual emergency situation caused by the COVID-19 in the United States, we are receiving a lot of inquiries about the FDA hand sanitizer registration process of Hand and wipe Sanitizer. So In this sense, the FDA issued a temporary
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What is the active ingredient in all FDA approved hand sanitizers? FDA issued a final rule on April 11 regarding ban certain dangerous active ingredients in OTC hand sanitizer products. After reviewing the safety and effectiveness of hand sanitizers, the normative concluded a previous determination from FDA that, 28 active ingredients, including triclosan and benzethonium chloride, are
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New FDA Sunscreen Regulations in the near future: What you need to know? Sunscreen products are classified as over-the-counter OTC products. FDA just released a new proposal of FDA sunscreen regulations. The proposed law requires products to be safe and effective. This update means that all non-approved sunscreen products currently sold in the
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FDA Food Labeling Changes: What Businesses Should Know The FDA food labeling changes impact businesses that have $10 million in annual revenue or more per year. Businesses must meet FDA food label requirements by January 1, 2020. The changes will impact the following on the Nutrition Facts Chart: • Daily values • Serving
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Is It Mandatory FDA Establishment Registration? Overview of When FDA Establishment Registration is Required FDA establishment registration varies depending on the FDA regulated product marketed and sold. Various types of FDA facility registration are discussed in the sections below. In general, prior to entering the market a company must classify the product, determine if FDA
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Selling Natural Health Products in Canada: What You Need to Know Consumers are demanding natural health products, and your business is equipped to meet that demand! But what are the requirements for selling a natural health product in Canada? Here are the 3 main requirements you need to know about before your product can hit
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Should I sell my cosmetics products to Europe or USA first? Whether you are a start-up company or an established company in your Home Country it comes the moment where you would like to export your products in new markets and increase your brand awareness or simply you want to sell directly in foreign markets.
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Cosmetic labeling: US FDA vs. EU Cosmetic labeling, what is the key difference between US and EU? U.S. and EU require for cosmetic companies who intend to distribute on the market to comply with cosmetic labeling requirements. As labeling is not only used to help inform consumers of a product’s intended use
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Product Information File (PIF) – What is it & How to create it? The Product Information File (PIF) includes all necessary elements such as a description of the product, a manufacturing method in compliance with Good Manufacturing Practice (GMP), labels and a cosmetic product Safety Report. This dossier aims at gathering all
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