Fragrance allergens update EUÂ The European Commission issued a new regulation (EU) 2023/1545 on July 27, 2023, updating the list of fragrance allergens in cosmetic products. Fragrance substances are commonly used in various cosmetic and household products, but they can cause contact allergies in some individuals. To protect consumers, the regulation aims for […]
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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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Update on UKCA Cosmetic Labeling and Marking Requirements: Extended Transition Period Announced by UK Government On November 14th, 2022, the Government of the United Kingdom made an important announcement regarding the transition period for UKCA cosmetic labeling and marking requirements. The deadline for compliance with UKCA marking requirements has been extended until December 31st, 2024.
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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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14 Key Questions About US Agents to Ensure Compliance with Medical Device Regulations Medical device regulations must be met if you want to sell your products in the United States. The following questions and answers will help you meet these requirements. Read more : Embracing the Future: Responsible Person & US Agent in the Era
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FDA: 2023 Medical Device User Fees Announcement Medical device user fees for the Fiscal Year 2023 are now available following an announcement from the U.S. Food and Drug Administration (FDA). The fiscal year runs from October 1, 2022 – September 30, 2023. All medical device facilities must pay the new fee amounts to keep their
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Key Developments in EU and UK Regulations: Early 2023 Updates 1. Recent Developments in Chemical Regulations In recent years, there has been growing scrutiny on the use and impact of chemicals in various aspects of modern life, with regulators and policymakers recognizing the role of innovative chemistry in addressing environmental challenges. The European Commission has
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FDA: 2023 Medical Device User Fees Announcement Medical device user fees for the Fiscal Year 2023 are now available following an announcement from the U.S. Food and Drug Administration (FDA). The fiscal year runs from October 1, 2022 – September 30, 2023. All medical device facilities must pay the new fee amounts to keep their
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What’s the Difference Between Food and Dietary Supplement Labeling in the United States and Canada? What’s the Difference Between Food and Supplement Labeling in the United States and Canada? Food and supplement companies must follow the labeling requirements in each jurisdiction they intend to sell their products in the U.S. and Canada. However, there
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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