Medical

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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Prorogation for submission and authorisations of DEHP application for MD and IVD
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Where we stand with MDR and IVDR European regulations about Medical Devices (Reg. EU 2017/745)...
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La tossicologia nel mondo dei dispositivi medici
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Il Regolamento (UE) 2017/745 dei dispositivi medici si pone l’obiettivo di elevare gli standard di qualità e...
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Cosa dice la nuova versione della ISO 10993-17?
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La nuova versione della ISO 10993-17 è stata pubblicata il 13 settembre 2023 a distanza...
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Latest Updates on Medical Devices
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Le novità introdotte nella 12a revisione delle SCCS Notes of guidance for the testing of cosmetic ingredients and their safety evaluation
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Il Comitato Scientifico per Sicurezza dei Consumatori (SCCS) è incaricato di valutare la sicurezza e...
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