Medical

The Commercialization of Medical Devices in Europe and the USA: Similarities and Differences
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The American Market Among the motivations that could drive a medical device manufacturer to commercialize...
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Urgent Need to Revise the Medical Devices Regulation
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The resolution on the urgent need to revise the Medical Devices Regulation, presented by several...
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Labelling of Cosmetic Products in the United States
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In the United States, cosmetic products must comply with specific labeling requirements mandated by the...
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Clinical Evaluation of Orphan Medical Devices
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What is a Orphan Medical Device? Orphan devices (ODs) are medical devices or their accessories,...
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MoCRA: How Chemsafe USA Can Secure Your Cosmetic Compliance
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Modernization of Cosmetics Regulation Act (MoCRA) The publication of the Modernization of Cosmetic Regulation Act...
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Microplastic Ban: Impact on Medical Devices and Cosmetic Products
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Starting from 17 October 2023, the EU will enforce a new regulation (COMMISSION REGULATION (EU)...
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Banned and Restricted Cosmetic Ingredients: What’s New
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In last month, two amendments to Regulation (EC) 1223/2009 have been published: Commission Regulation (EU)...
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Global Cosmetic Regulations: a Brief Guide for the Complex Landscape of EU, UK, US, and China
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In a constantly changing cosmetic regulatory landscape, we have left behind a year full of...
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Regulatory Toxicology: Here’s how Chemsafe can help you
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What is regulatory toxicology Regulatory toxicology is a particular branch of experimental toxicology, historically derived...
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EU reference laboratories for high-risk IVDs
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In a landmark decision, the European Commission, on December 5, 2023, has officially designated five...
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