3.

Within 180 days of receipt of the conclusions of the evaluation, the Agency shall prepare and submit to the Commission an opinion on the authorisation of the biocidal product. If the Agency recommends the authorisation of the biocidal product, the opinion shall contain at least the following elements: a statement on whether the conditions laid down in Article 19(1) are fulfilled, and a draft summary of biocidal product characteristics, as referred to in Article 22(2); where relevant, details of any terms or conditions which should be imposed on the making available on the market or use of the biocidal product; the final assessment report on the biocidal product.

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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.