Blog

40 Hazardous Chemicals Added to Annex I of Prior Informed Consent (PIC) Regulation
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  The PIC Regulation (EU) No 649/2012 of the European Parliament and of the Council...
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FDA’s Quality System Regulation (QSR) and cGMP for Medical Devices: What Manufacturers Should Know
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Understanding the FDA’s Quality Requirements for Medical Devices For medical device manufacturers, quality and compliance...
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January Regulatory Updates
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Food: EFSA Updates on Terrestrial Ecotoxicology and Biodiversity Impact Assessment Mandate on Terrestrial Ecotoxicology: EFSA...
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Understanding Health Claims: FDA Authorization and Qualification
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Health claims on food labels play a critical role in informing consumers about the relationship...
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2024 in a Nutshell
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2024 proved to be a year of great ferment in terms of regulatory activity aimed...
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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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Novel Food Guidance: Latest Updates
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In September and October 2024, the European Food Safety Authority (EFSA) revised its guidance concerning...
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November Regulatory Updates
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CLP: ECHA Updates CLP Regulation Guidance: Key Changes Explained This November, ECHA published an updated...
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Machine Learning in Early Prediction of Metabolism of Drugs
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Marta Lettieri, Virginia Carlucci and Marco Rodda have contributed to the latest edition of Computational...
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Guidance on the New CLP Hazard Classes
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Humans and the environment are in perpetual contact with substances and mixtures from different sources....
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