Your biocidal product under the transitional regime
The active substance of your biocidal product (BP) is an existing active substance, but not yet approved? You want to market your biocidal product in certain EU countries now? We would be pleased to support you in this mission. We determine the requirements of individual European Member States specifically for your BP and support you in compiling the necessary documents. On your behalf, we carry out the registrations, notifications or approvals in those EU countries that are relevant for you and also support you in special cases and in communication with authorities.
What are the deadlines? Depending on the active substance, transitional rules may apply until 2024. Product registration under the transitional regime can be simple and inexpensive, but some Member States require the submission of a complex and comprehensive dossier for product authorisation. The requirements of individual countries always depend on the active substances and the product type of your biocidal product.
We are happy to support you in the legally compliant marketing of your products in various countries of the European Union (EU) and the European Economic Area (EEA) as well as Switzerland.
We investigate in which country a registration is worthwhile for you and determine a cost-effective strategy. Contact us (email@example.com) to find out the requirements for the distribution of your BP.
We also offer biocide training courses tailored specifically to your needs.