Division 3 The ... reference laboratory shall be responsible, in particular, for:F1 F2

United Kingdom

(a)
F3...
(b)
F4...
(c)
evaluating the data provided by the applicant for authorisation for placing the food or feed on the market, for the purpose of testing and validation of the method for sampling and detection;
(d)
testing and validating the method for detection, including sampling and identification of the transformation event and, where applicable, for the detection and identification of the transformation event in the food or feed;
(e)
submitting full evaluation reports to the Authority.

Annotations

F1: Substituted by Commission Regulation (EC) No 1981/2006 of 22 December 2006 on detailed rules for the implementation of Article 32 of Regulation (EC) No 1829/2003 of the European Parliament and of the Council as regards the Community reference laboratory for genetically modified organisms (Text with EEA relevance).
F2: Word in Annex para. 3 omitted (31.12.2020) by virtue of The Genetically Modified Food and Feed (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/705), regs. 1, 41(c)(i); 2020 c. 1, Sch. 5 para. 1(1)
F3: Annex para. 3(a) omitted (31.12.2020) by virtue of The Genetically Modified Food and Feed (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/705), regs. 1, 41(c)(ii); 2020 c. 1, Sch. 5 para. 1(1)
F4: Annex para. 3(b) omitted (31.12.2020) by virtue of The Genetically Modified Food and Feed (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/705), regs. 1, 41(c)(ii); 2020 c. 1, Sch. 5 para. 1(1)

F1: Word in Annex title omitted (31.12.2020) by virtue of The Genetically Modified Food and Feed (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/705), regs. 1, 41(a); 2020 c. 1, Sch. 5 para. 1(1)