#CLP

November Regulatory Updates
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Medical Devices: ISO 10993-1:2025 finally released, 6th edition of the standard on Biological risk evaluation...
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October Regulatory Updates
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Medical Devices: FDA Draft Guidance on Quality Management System Regulation (QMSR) The FDA has published...
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Stop-the-Clock in the CLP Regulation, a mechanism that is changing Chemical Compliance between 2025 and 2028
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The European chemical industry is entering a period of major regulatory shift, with the aim...
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September Regulatory Updates
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Medical Devices: Consultation Open: EU seeks to simplify MDR and IVDR Frameworks The European Commission...
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September 16: World Ozone Day and the Responsibility of Chemical Management
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Every year on September 16, we observe the International Day for the Preservation of the...
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August Regulatory Updates
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Medical Devices: European Commission Confirms Continued Use of Titanium Dioxide in Medicinal Products Background On...
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July Regulatory Updates
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Medical Devices: MDCG Publishes Position Paper on UDI-DI Timelines for Optical Devices Implementation Deadlines Set...
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Talc: New Harmonized Classification Proposal – What Changes for Companies?
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The Committee for Risk Assessment (RAC) has adopted an opinion that could radically change how...
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June Regulatory Updates
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CLP: 23rd ATP to CLP Regulation Published Key Update The European Commission has published Delegated...
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EU Wide Restriction on N,N-dimethylacetamide (DMAC) and 1-ethylpyrrolidin-2-one (NEP)
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Last week, on June 2nd 2025, The European Commission has adopted a restriction on DMAC...
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