2.

From the date on which a biocidal product is authorised, the Agency shall make publicly and easily available free of charge the following up-to-date information: the terms and conditions of the authorisation; the summary of the biocidal product characteristics; and analytical methods referred to under Sections 5.2 and 5.3 of Title 1, and Section 5.2 of Title 2 of Annex III.

← art_67__para_1__point_h__text_1 · All articles · art_67__para_2__text_1 →

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