Article 1 Subject matterF1

United Kingdom

This Regulation lays down the procedure applicable where an authorisation is sought for a product (the ‘same product’) which is identical to another single biocidal product, biocidal product family, or individual product of a biocidal product family which has been authorised or registered F2in the United Kingdom in accordance with Directive 98/8/EC of the European Parliament and of the Council^f1 or F3authorised or registered in the United Kingdom in accordance with Regulation (EU) No 528/2012, F4or authorised or registered in Great Britain in accordance with this Regulation, or for which an application for such authorisation has been submitted (the ‘related reference product’), with regard to all the latest information submitted in relation to the authorisation or registration, except information which can be the subject of an administrative change in accordance with Commission Implementing Regulation (EU) No 354/2013^f2.

Annotations

Textual amendments

F1: Substituted by Commission Implementing Regulation (EU) 2016/1802 of 11 October 2016 amending Implementing Regulation (EU) No 414/2013 specifying a procedure for the authorisation of same biocidal products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance).
F2: Words in Art. 1 inserted (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. 195(a) (as substituted by S.I. 2020/1567, reg. 1(2), Sch. 2 para. 64); 2020 c. 1, Sch. 5 para. 1(1)
F3: Words in Art. 1 inserted (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. 195(b) (as substituted by S.I. 2020/1567, reg. 1(2), Sch. 2 para. 64); 2020 c. 1, Sch. 5 para. 1(1)
F4: Words in Art. 1 inserted (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. 195(c) (as substituted by S.I. 2020/1567, reg. 1(2), Sch. 2 para. 64; 2020 c. 1, Sch. 5 para. 1(1)

Footnotes

f1: Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 concerning the placing of biocidal products on the market ( OJ L 123, 24.4.1998, p. 1 ).
f2: Commission Implementing Regulation (EU) No 354/2013 of 18 April 2013 on changes of biocidal products authorised in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council ( OJ L 109, 19.4.2013, p. 4 ).