1.

A Biocidal Products Committee is hereby established within the Agency. The Biocidal Products Committee shall be responsible for preparing the opinion of the Agency on the following issues: applications for approval and renewal of approval of active substances; review of approval of active substances; applications for inclusion in Annex I of active substances meeting the conditions laid down in Article 28 and review of the inclusion of such active substances in Annex I; identification of active substances which are candidates for substitution; applications for Union authorisation of biocidal products and for renewal, cancellation and amendments of Union authorisations, except where the applications are for administrative changes; scientific and technical matters concerning mutual recognition in accordance with Article 38; at the request of the Commission or of Member States’ competent authorities, any other questions that arise from the operation of this Regulation relating to technical guidance or risks to human health, animal health or the environment.

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Source: EUR-Lex (Cellar) · retrieved 2026-10-29 · Text as adopted (Official Journal); later amendments are not incorporated in this text.