1.

Applicants wishing to seek the mutual recognition in parallel of a biocidal product which has not yet been authorised in accordance with Article 17 in any Member State shall submit to the competent authority of the Member State of its choice (‘the reference Member State’) an application containing: the information referred to in Article 20; a list of all other Member States where a national authorisation is sought (‘the Member States concerned’). The reference Member State shall be responsible for the evaluation of the application.

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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.