Blog

Understanding the Reflection Paper on the Qualification of Non-Mutagenic Impurities: A Regulatory Perspective
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Introduction In the complex world of pharmaceutical development, ensuring drug safety and efficacy is paramount....
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April Regulatory Updates
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Food: Safe2Eat 2025: EFSA relaunches campaign to boost EU consumer confidence in food safety Fifth...
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Glyphosate: The Best-Selling Herbicide of All Time
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A Brief History Glyphosate, chemically known as N-phosphonomethyl-glycine, was discovered in the 1970s by American...
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April 22, Earth Day: A Closer Look at EU Regulation 2025/40
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Earth Day is an annual event held every April 22 to raise public awareness about...
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GRAS Procedure: Looking to the Future while Anchored in the Past
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What’s a GRAS Procedure?  The Generally Recognized as Safe (GRAS) procedure is a regulatory framework...
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ISO 22716: Good Practices to Follow During Cosmetic Products Manufacturing
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In the dynamic and highly scrutinized world of cosmetics, ensuring product safety and quality is...
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March Regulatory Updates
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Cosmetics: ​European Commission Launches Evaluation of Cosmetic Products Regulation Objective of the Review The European...
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Ethanol Re-Classification: Is It just a Disinfectant Issue for Regulation 528/2012?
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These days, anyone who deals with disinfectants cannot help but look with fear at the...
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FDA Issues Draft Guidance on AI in Drugs and Devices
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FDA Releases Draft Guidance on AI in Drug and Medical Device Development The U.S. Food...
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The new CLP Regulation (2024/2865) and 2023/707 and their impact on SDSs
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The regulatory framework for the classification, labelling, and packaging of substances and mixtures continues to...
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