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Division 2.3 By way of derogation from point 2.1, the competent authority may provide that supervised residue trials performed on their constituent territory in accordance with Section 6 ‘Residues in or on treated products, food and feed’ on plant protection products containing active substances already on the market on or before 25th July 1993 shall be conducted by official or officially-recognised testing facilities or organisations which satisfy at least the requirements under points 2.2 and 2.3 of the introduction to the Annex to Regulation (EU) No 545/2011.F1F2F3F4

United Kingdom

Original text. Later amendments are not shown.

This derogation applies for supervised residue trials which actually started on or before 31 December 1997.

Annotations

Textual amendments

F1

Repealed (subject to transitional measures in Arts. 3, 4) by Commission Regulation (EU) No 283/2013 of 1 March 2013 setting out the data requirements for active substances, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market Text with EEA relevance.

F2

Words in Annex Introduction point 2.3 substituted (31.12.2020) by The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 (S.I. 2019/556), regs. 1(1), 16(5)(a)(vi)(aa); 2020 c. 1, Sch. 5 para. 1(1)

F3

Word in Annex Introduction point 2.3 inserted (31.12.2020) by The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 (S.I. 2019/556), regs. 1(1), 16(5)(a)(vi)(bb); 2020 c. 1, Sch. 5 para. 1(1)

F4

Words in Annex Introduction point 2.3 substituted (31.12.2020) by The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 (S.I. 2019/556), regs. 1(1), 16(5)(a)(vi)(cc); 2020 c. 1, Sch. 5 para. 1(1)