2.

Within 30 days of acceptance, the receiving competent authority shall validate the application if it complies with the following requirements: the relevant information referred to in Article 20 has been submitted; and the applicant states that it has not applied to any other competent authority for a national authorisation for the same biocidal product for the same use(s). In the context of the validation referred to in the first subparagraph, the receiving competent authority shall not make an assessment of the quality or the adequacy of the data or justifications submitted.

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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.