#Chemsafe

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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June Regulatory Updates
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Biocides: Concerns Over Surge in Animal Testing Due to Endocrine Disruptors Deadline Deadline Imposes Increased...
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Milestones of Food Supplements’ Marketing Procedure: EU and US in Comparison
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The global food supplement market has been experiencing steady growth for the last few years....
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New REACH Restriction of D4, D5, and D6 Substances
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On May 16, the European Commission published Regulation 1328/2024, which amends Annex XVII of Regulation...
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May Regulatory Updates
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Biocides: European Commission Extends Biocides Review Program Program Extension: The European Commission has officially extended...
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The Labeling of Plant Protection Products
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What is the purpose of a product label? The label must offer consumers information about...
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New ERA Guideline released on March 2024 by EMA. What changes in the Environmental Risk Assessment of medicines (ERA)?
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What is the environmental impact assessment of active pharmaceutical ingredients? Environmental impact assessment of active...
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Microorganisms in Food Production: a New Trend
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Consumer safety in first place Throughout history, microorganisms have played a pivotal role in food...
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April Regulatory Updates
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Biocides: IUCLID Version 8.0.1 Launches with Comprehensive Updates New Format Enhancements: IUCLID version 8.0.1 is...
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New drug directive approved on April 11, 2024 by the European Parliament. What changes in the environmental risk assessment of medicines (ERA)?
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What does it mean to perform an environmental impact assessment of active pharmaceutical ingredients? Environmental...
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