Simplified authorisations products containing low risk substances

The simplified authorisation is possible for biocidal products that are based on low-risk substances included in Annex I of the Biocidal Products Regulation.

Please note: Annex I of the Regulation is not the same as Annex I of the Directive. Substances from Annex I of the Directive are now included in the Union list of approved active substances.

After a simplified authorisation of a biocidal product in one member state, the biocidal product can be placed on the market in any other member states after notification. The notification must be made no later than 30 days before placing the biocidal product on the market in the territory of the member state.