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