Embracing the Future: Responsible Person & US Agent in the Era of MoCRAÂ On December 29th, 2022, the cosmetic industry witnessed a groundbreaking change in regulatory requirements (21 U.S.C., Sec. 321-392), the most substantial update since 1938. This legislation, known as MoCRA, brings forth fresh obligations and signals a significant shift in how […]
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MoCRA: The US FDA released the first guideline for Cosmetic product listing and establishment registration It is recent news that the US Food and Drug Administration (FDA) released a draft Guidance on the new cosmetic MoCRA regulations. The MoCRA cosmetic guidelines give information to the cosmetic industry on how to list cosmetic products and
How to get a DUNS number for food facility registration with the FDA In the United States, both domestic and foreign facilities engaged in the manufacturing, processing, packing, or storage of food intended for human or animal consumption are required by law to register with the U.S. Food and Drug Administration (FDA). This
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A Comprehensive Look at Post-Market Surveillance for Cosmetics in Europe and the USA Cosmetics have become an essential part of our daily lives, with millions of people around the world using them every day. Cosmetics are used for various purposes, such as enhancing one’s beauty, maintaining personal hygiene, and improving overall well-being. However, the
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FDA Halts VCRP in Anticipation of Compulsory Cosmetics Registration The FDA’s latest cosmetic regulation update has shaken the beauty industry. According to the constituent update on March 27, 2023, cosmetic companies can no longer submit to the Voluntary Cosmetics Registration Program (VCRP). Now, they must use a new program currently in development by the FDA
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10 Essential Facts About the Modernization of Cosmetics Regulation Act (MoCRA) of 2022 Breaking New Ground: The Modernization of Cosmetics Regulation Act (MoCRA) of 2022 The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) is a comprehensive legislation that enhances the FDA’s authority over cosmetic products, aiming to ensure their safety for consumers. Here are
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California Cosmetics Allergens Labeling Requirements Do Businesses Have to List Allergens on Cosmetic Labels? An estimated 10% of people experience allergy-related irritation or hypersensitivity from cosmetic products. The severity of allergic reactions can range from mild dermatitis to anaphylaxis, a potentially life-threatening reaction. Of course, allergens are always a concern with any consumer product, but
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CBD FDA Labeling Requirements Remains a Grey Area Filled with Concerns The U.S. Food and Drug Administration (FDA) has increased its scrutiny of CBD labeling and marketing practices. Hemp-based product uses are increasing, and many investors and consumers are unaware of the grey areas of the industry. Stakeholders in the industry have pushed for clarity
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FDA Cosmetic Approval: What You Need to Know About The FDA regulates drugs and cosmetics, but when a cosmetic is considered a drug, it can become difficult for manufacturers to discern whether their product is classified as an FDA OTC drug or a cosmetic and if requires FDA cosmetic approval. FDA OTC Drug product
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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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