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Maintain good HSE risk management
Home fragrances (candles, incense, diffusers, room sprays) are increasingly scrutinized for VOC emissions and potential impacts on indoor air quality. This article clarifies why “natural vs synthetic” is a misleading safety proxy: what matters is the risk of the finished product—hazard combined with real-world exposure under foreseeable use. It highlights why emissions vary widely across product types, formulations, and usage conditions (combustion, ventilation, duration), and connects the risk assessment approach to EU Regulation 2023/988 on general product safety.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Union authorisation allows companies to market biocidal products across the EU with a single approval, bypassing national authorisations. The process involves dossier submission, evaluation by competent authorities, and a final decision by the European Commission.
Learn about the requirements for labeling products as Cruelty-Free in Europe, the evolution of animal testing laws, and the importance of compliance for imported cosmetics. Stay informed to avoid false claims and ensure your products meet regulations.
Learn about the process of obtaining marketing authorisation for biocidal products at national and European levels. Discover the different types of authorisations, including Union, National, and Simplified, and understand the requirements and timelines involved in each.
Learn about the post-registration processes for REACH compliance. Understand the criteria for dossier completeness, compliance checks, substance evaluation, and more. Stay updated, communicate with your supply chain, and ensure compliance to avoid extra costs.
EcoMundo presents you with 4 key points for successfully conducting your Alternatives Analysis, a crucial step in the creation of the Authorization dossier.
Learn how to navigate REACH regulations if you haven't registered your substances yet. Discover loopholes, tonnage band calculations, and what to do if you create a new substance post-May 2018 deadline. Plus, find out about exemptions and recommendations for compliance.
