1.

The applicant for an authorisation shall submit the following documents together with the application: for biocidal products other than biocidal products meeting the conditions laid down in Article 25: a dossier or letter of access for the biocidal product satisfying the requirements set out in Annex III; a summary of the biocidal product characteristics including the information referred to in points (a), (b) and (e) to (q) of Article 22(2), as applicable; a dossier or a letter of access for the biocidal product satisfying the requirements set out in Annex II for each active substance in the biocidal product; for biocidal products that the applicant considers meet the conditions laid down in Article 25: a summary of the biocidal product characteristics as referred to in point (a)(ii) of this paragraph; efficacy data; and any other relevant information in support of the conclusion that the biocidal product meets the conditions laid down in Article 25.

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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.