OpenLegislation

Division 55

United Kingdom

Original text. Later amendments are not shown.

The purpose of the evaluation is to establish whether or not the product complies with the criteria set down in point (b) of Article 19(1). The F1competent authority shall reach its conclusion as a result of the integration of the risks arising from each active substance together with the risks from each substance of concern present in the biocidal product, based on the assessment carried out in accordance with points 13 to 54 of this Annex.

Annotations

Textual amendments

F1

Words in Annex 6 para. 55 substituted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 143(11); 2020 c. 1, Sch. 5 para. 1(1)