# Commission Regulation (EU) No 1141/2010 of 7 December 2010 laying down the procedure for the renewal of the inclusion of a second group of active substances in Annex I to Council Directive 91/414/EEC and establishing the list of those substances (Text with EEA relevance), Article 1: Scope

Extent: E+W+S+N.I.

(1.) This Regulation lays down the procedure for the determination of the existing renewal application by the relevant competent authority as assessing competent authority.
(2.) The “existing renewal application” is the application for the renewal of the approval of the active substance famoxadone which—
(a) was made to the United Kingdom as rapporteur Member State in accordance with Article 4 as it had effect immediately before IP completion day, and
(b) is taken as being made under this Regulation and Article 15(1) of Regulation (EC) No 1107/2009 on the date on which it was made.
(3.) Anything done under this Regulation as it had effect immediately before IP completion day in relation to the existing renewal application—
(a) by the United Kingdom as rapporteur Member State;
(b) by the European Food Safety Authority;
is taken to have been done by the relevant competent authority as the assessing competent authority.
(4.) In this Article—
(a) “rapporteur Member State” has the meaning given in Article 2(c) as it had effect immediately before IP completion day;
(b) the “relevant competent authority” is the Secretary of State.

---
Source: https://www.legislation.gov.uk/eur/2010/1141/article/1 (the official version)
Page: https://openlegislation.uk/eu-regulation-2010-1141/article-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.