Cosmereg, Author at Cosmereg

Update on UKCA Cosmetic Labeling and Marking Requirements

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 […]

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FDA VCRP Discontinuation

USA Cosmetic Regulations / Cosmereg

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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Proposed regulations for fragrance allergen ingredient labeling in Canada

Canada Cosmetic Regulations / Cosmereg

Proposed regulations for fragrance allergen ingredient labeling in Canada Health Canada is proposing new regulations that would require fragrance allergen ingredient labeling on all cosmetic and personal care products sold in Canada. The proposal is aimed at increasing transparency and protecting consumers from potential allergic reactions to fragrance ingredients. Fragrance ingredients are commonly found

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14 US Agent Questions to Know to Meet Medical Device Regulations

US FDA Medical Devices / Cosmereg

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. 1. Are You Required to Appoint a US Agent? Yes. The FDA

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10 Essential Facts About the Modernization of Cosmetics Regulation Act (MoCRA) of 2022

USA Cosmetic Regulations / Cosmereg

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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Key Developments in EU and UK Regulations: Early 2023 Updates

EU Cosmetic Regulations / Cosmereg

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

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FDA: 2023 Medical Device User Fees Announcement

US FDA Medical Devices / Cosmereg

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?

Canada Dietary Supplement NHP NPN, US FDA Dietary Supplements, US FDA food regulations / Cosmereg

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

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California Cosmetics Allergens Labeling Requirements

USA Cosmetic Regulations / Cosmereg

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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Dietary Supplement Labeling Guide

US FDA Dietary Supplements / Cosmereg

Dietary Supplement Labeling Guide: Understanding Claims, Labels and Regulations Dietary supplements are in high demand, and businesses offering or planning to offer any of the following will need to meet the strict claim, FDA label requirements for dietary supplements: Botanicals Herbs Minerals Protein bars Other supplements Health and nutrition are big business, and while

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Author name: Cosmereg

Update on UKCA Cosmetic Labeling and Marking Requirements

FDA VCRP Discontinuation

Proposed regulations for fragrance allergen ingredient labeling in Canada

14 US Agent Questions to Know to Meet Medical Device Regulations

10 Essential Facts About the Modernization of Cosmetics Regulation Act (MoCRA) of 2022

Key Developments in EU and UK Regulations: Early 2023 Updates

FDA: 2023 Medical Device User Fees Announcement

What’s the Difference Between Food and Dietary Supplement Labeling in the United States and Canada?

California Cosmetics Allergens Labeling Requirements

Dietary Supplement Labeling Guide

US FDA Regulations

Health Canada Regulations

EU/UK Regulations

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