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08/06/1994
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What Is MoCRA? A Guide to US FDA Cosmetics ComplianceMoCRA: A New Chapter in U.S. Cosmetics Regulation For nearly 85 years, U.S. cosmetics regulation ran on rules set by the Federal Food, Drug, and Cosmetic Act of 1938. That changed on December 29, 2022, when the Modernization of Cosmetics Regulation Act (MoCRA) became law as part of the Consolidated Appropriations Act of 2023. It's the largest expansion of FDA authority over cosmetics since that...0 Comments 0 Shares 96 Views 0 ReviewsPlease log in to like, share and comment!
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What Is MoCRA? A Guide to US FDA Cosmetics ComplianceMoCRA Explained: A New Era for Cosmetics Regulation in the U.S. For over 80 years, cosmetics in the United States operated under a regulatory framework that hadn't changed much since 1938. That changed on December 29, 2022, when Congress passed the Modernization of Cosmetics Regulation Act (MoCRA) as part of the Consolidated Appropriations Act of 2023. It's widely considered the most sweeping...0 Comments 0 Shares 96 Views 0 Reviews
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Australia PIC/S GMP Framework for Dietary Supplements |FreyrSelling Supplements in Australia? Why PIC/S GMP Rules Could Change Your Whole Playbook If you're a dietary supplement or nutraceutical company looking at Australia as your next market, there's a regulatory reality worth understanding before you get too far into planning: Australia is one of the strictest health-product markets in the world, and a lot of that comes down to one framework —...0 Comments 0 Shares 91 Views 0 Reviews
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EU & Canada Fragrance Allergen Regulations Guide| FreyrNew Fragrance Allergen Rules in the EU and Canada: What Cosmetic Brands Need to Know Contact dermatitis linked to cosmetics is frequently traced back to fragrance allergens, and regulators are responding with stricter disclosure rules. The latest changes in the European Union and Canada show two of the world's biggest cosmetic markets moving toward the same goal: clearer labels, better-informed...0 Comments 0 Shares 78 Views 0 Reviews
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Regulatory Inspections: How Authorities Review SDS & ClaimsThe New Reality of Chemical Compliance Inspections: What Regulators Are Really Looking For Chemical companies are facing a different kind of scrutiny these days. It's not enough to have an SDS on file — regulators want proof that every hazard claim is scientifically sound, every document tells the same story, and every marketing line matches what's actually in the data. This shift is...0 Comments 0 Shares 197 Views 0 Reviews
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EU CLP Regulation Update: Compliance Checklist for CompaniesUpdated EU CLP Rules: A Practical Breakdown for Chemical Businesses The EU has revised its Classification, Labelling and Packaging (CLP) Regulation again, and this round carries enough weight that manufacturers, importers, and exporters of chemicals should plan a real response rather than a quick skim. What's in the Update 27 newly added harmonized classifications 16 classifications revised 7...0 Comments 0 Shares 152 Views 0 Reviews
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What Is GMP for Food Products? Global Regulations ExplainedGMP Harmonization: Aligning Food Safety Standards in a Globalized Supply Chain Food and dietary supplement manufacturers operate under a system known as Good Manufacturing Practices (GMP) — a set of procedures and controls built to keep production safe, sanitary, and consistent. Rather than catching problems only at the finish line through final product testing, GMP works by embedding...0 Comments 0 Shares 168 Views 0 Reviews
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PPWR Substances of Concern: What Changes in August 2026?PPWR Substances of Concern: What the Commission's FAQ Clears Up Before the August 2026 Deadline With Regulation (EU) 2025/40 — the Packaging and Packaging Waste Regulation (PPWR) — set to take full effect on 12 August 2026, the European Commission has released an FAQ addressing one of the regulation's more complex areas: substances of concern (SoC) in packaging. The intent behind...0 Comments 0 Shares 184 Views 0 Reviews
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PPWR Substances of Concern: What Changes in August 2026?What the EU's PPWR FAQ Means for Substances of Concern in Packaging As the 12 August 2026 application date for the Packaging and Packaging Waste Regulation (Regulation (EU) 2025/40) draws closer, the European Commission has issued an FAQ addressing how substances of concern (SoC) will be handled under the new framework. The regulation is designed to cut down on harmful substances in packaging...0 Comments 0 Shares 191 Views 0 Reviews
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Front-of-Pack Labeling for Supplements | Compliance GuideFront-of-Pack Labeling: A Growing Compliance Consideration for Dietary Supplement Manufacturers Front-of-Pack Labeling (FOPL) has evolved from a consumer information tool into a significant regulatory mechanism shaping nutrition policy worldwide. Increasingly, regulators are using FOPL frameworks to communicate nutrient-related risks, influence purchasing decisions, and support public health...0 Comments 0 Shares 186 Views 0 Reviews
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Front-of-Pack Labeling for Supplements | Compliance GuideFront-of-Pack Labeling: A Growing Compliance Imperative for Dietary Supplements Front-of-Pack Labeling (FOPL) is no longer a peripheral consideration in nutrition policy. It has evolved into a significant regulatory mechanism for communicating nutrient-related risks and, increasingly, influencing market access. For dietary supplement manufacturers, this shift is particularly important as...0 Comments 0 Shares 205 Views 0 Reviews
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OSHA Hazard Communication Standard (HCS): ExplainedOSHA Hazard Communication Standard: What Every Workplace Needs to Know Most workplace chemical incidents don't happen because people were reckless. They happen because someone didn't have the right information at the right time. That's exactly the problem the OSHA Hazard Communication Standard was built to solve. The "Right-to-Know" Standard The Hazard Communication Standard (HCS) is a federal...0 Comments 0 Shares 288 Views 0 Reviews
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