[F1 5. On request by the [F2appropriate authority], the [F3reference laboratory] may also be responsible for conducting special analytical or other related studies in a manner similar to the duties and tasks referred to in point 2. This may be the case, in particular, for existing products notified under Article 10 and included in the Register and for the period until an application for authorisation under Article 10(2) is submitted in accordance with Article 10(2). ]U.K.Textual Amendments
F2Words in Annex 2 point 5 substituted (31.12.2020) by The Animal Feed (Amendment) (EU Exit) Regulations 2019 (S.I. 2019/654), regs. 1, 33(h)(i); 2020 c. 1, Sch. 5 para. 1(1)
F3Words in Annex 2 point 5 substituted (31.12.2020) by The Animal Feed (Amendment) (EU Exit) Regulations 2019 (S.I. 2019/654), regs. 1, 33(h)(ii); 2020 c. 1, Sch. 5 para. 1(1)
Textual Amendments
F2Words in Annex 2 point 5 substituted (31.12.2020) by The Animal Feed (Amendment) (EU Exit) Regulations 2019 (S.I. 2019/654), regs. 1, 33(h)(i); 2020 c. 1, Sch. 5 para. 1(1)
F3Words in Annex 2 point 5 substituted (31.12.2020) by The Animal Feed (Amendment) (EU Exit) Regulations 2019 (S.I. 2019/654), regs. 1, 33(h)(ii); 2020 c. 1, Sch. 5 para. 1(1)
Textual Amendments
F1Substituted by Commission Regulation (EC) No 378/2005 of 4 March 2005 on detailed rules for the implementation of Regulation (EC) No 1831/2003 of the European Parliament and of the Council as regards the duties and tasks of the Community Reference Laboratory concerning applications for authorisations of feed additives (Text with EEA relevance).