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National authorisations (NAs) of biocidal products (BPs) issued by competent authorities of the Member States (MSCAs) or for Union authorisations (UAs) by the European Commission (COM) are only valid for the approved terms and conditions stated therein. The relevant provisions on amendments of N...

The Guidance on the Biocidal Products Regulation (BPR) is to be applied to applications for active substance approval and product authorisation as submitted from 1 September 2013, the date of application (DoA) of the Biocidal Product Regulation (the BPR). This document describes the BPR obligati...

The authorisation of a biocidal product (BP) can be recognised in other Member States (MSs) in accordance with the mutual recognition (MR) procedures to avoid duplication of the evaluation. There are two procedures: mutual recognition in sequence (MRS) which is relevant where there is an existin...

The EU Ecolabel promotes Europe’s transition to a zero pollution and circular economy, by minimising products’ impact on the environment. Materials are carefully selected to stay in a loop, so new products begin when old ones end. EU Ecolabel products: minimise waste, pollution and CO2 emissions...