The European Regulation (EC) No.1272/2008 on classification, labelling and packaging of substances and mixtures (‘the CLP Regulation’ or ‘CLP’) applies to all EU Member States.
CLP requires manufacturers, importers, downstream users and distributors to communicate the identified hazards of a substance or mixture to the other parties in the supply chain, including to consumers. The regulation requires products with hazardous properties to be labelled in accordance with CLP before being placed on the market. CLP requires products containing any ingredients that have been classified as Category 1A and 1B carcinogens to be labelled as carcinogenic.
Therefore, with respect to the BREEAM Category 1A and 1B carcinogens emission limit criteria, for products marketed in EU Member States, if a product’s safety information (e.g. safety data sheet) or a manufacturer’s declaration confirms that that the product does not need to be labelled as a Category 1A or 1B carcinogen in accordance with CLP, then this information would be an acceptable form of evidence for demonstrating compliance with the criteria