OpenLegislation

Division 13

United Kingdom

Original text. Later amendments are not shown.

The data submitted in support of an application for authorisation of a biocidal product shall be validated by the F1... competent authority in accordance with the relevant articles of the Regulation. After validation of these data the F2competent authority shall utilise them by carrying out a risk assessment based on the proposed use. Information submitted in the framework of Regulation (EC) No 1907/2006 shall be taken into account where appropriate.

Annotations

Textual amendments

F1

Words in Annex 6 para. 13 omitted (31.12.2020) by virtue of 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(9)(a); 2020 c. 1, Sch. 5 para. 1(1)

F2

Words in Annex 6 para. 13 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(9)(b); 2020 c. 1, Sch. 5 para. 1(1)