As of 6 February 2026, the Regulation of the Minister of Health on fees for activities related to the authorisation of a biocidal product for placing on the market enters into force.
The Regulation of the Minister of Health of 29 January on fees for activities related to the authorisation of a biocidal product for placing on the market has been published in the Journal of Laws. The Regulation governs the fees charged by the Authority in Poland, including:
- Submission of an application for the granting of an authorisation for placing a biocidal product on the market
- Making a change to the authorisation for placing on the market
- Making a change of the responsible entity being the holder of the authorisation
The fees cover both authorisations for placing a biocidal product on the market under the national procedure as well as under the European procedure.
The update concerns the fee structure and the level of rates related to the evaluation of active substances, the granting of authorisations for biocidal products, and advisory services of the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products.
Source: Journal of Laws 2026, item 126
Ekotox website: https://ekotox.eu/biocides/
