The draft Law aims to regulate legal relations related to the approval of active substances of biocidal products, state registration, production, market placement, circulation and the safe use of biocidal products and processed products for human and animal health, and the environment. It aims also to define the rights and obligations of enterprises, institutions, organisations and individuals, along with the relevant powers. The draft Law proposes the designation of an authorized body - a state enterprise (institution or organization) - which, empowered by the central executive authority responsible for the formation and implementation of state healthcare policy, will be tasked with evaluating materials for the approval, renewal, or revision of active substances. The body will also prepare expert opinions with proposals for approval or refusal of approval, renewal, or revision of active substances, as well as expert opinions on the possibility of state registration of biocidal products and processed products. Services for evaluation of materials for approval, renewal or revision, state registration, state registration under a simplified procedure or refusal of registration of active substances shall be provided by the authorised body for a fee, in accordance with the agreement between the applicant and the authorised body. The procedure for setting the fee for services provided by the authorized body in evaluating applications for the renewal of approval of active…