2.

Member States shall make the necessary arrangements for official controls to be carried out in order to enforce compliance with this Regulation. In order to facilitate such enforcement, manufacturers of biocidal products placed on the Union market shall maintain, in relation to the manufacturing process, appropriate documentation in paper or electronic format relevant for the quality and safety of the biocidal product to be placed on the market and shall store production batch samples. The documentation shall include as a minimum: safety data sheets and specifications of active substances and other ingredients used for manufacturing the biocidal product; records of the various manufacturing operations performed; results of internal quality controls; identification of production batches. Where necessary in order to ensure uniform application of this paragraph, the Commission may adopt implementing acts in accordance with the examination procedure referred to in Article 82(3). Measures taken pursuant to this paragraph shall avoid causing disproportionate administrative burden to economic operators and Member States.

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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.