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Commission Regulation (EU) No 544/2011 (repealed)Show full title
Commission Regulation (EU) No 544/2011 of 10 June 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances (Text with EEA relevance) (repealed)
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[F12.Test and analysesU.K.
2.1.Tests and analyses must be conducted in accordance with the principles laid down in [F2Annex 1 to] Directive 2004/10/EC of the European Parliament and of the Council where testing is done to obtain data on the properties and/or safety with respect to human or animal health or the environment.U.K.Textual Amendments
Textual Amendments
2.2.By way of derogation from point 2.1, [F3the competent authority] may provide that tests and analyses, performed on their [F4constituent] territory in order to obtain data on the properties and/or safety of the active substances with respect to honey-bees and beneficial arthropods other than bees shall be conducted by official or officially-recognised testing facilities or organisations which satisfy at least the requirements as set out under points 2.2 and 2.3 of the introduction to the Annex to Commission Regulation (EU) No 545/2011.U.K.
This derogation applies to trials which actually started on or before 31 December 1999.
Textual Amendments
F3Words in Annex Introduction point 2.2 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)(v)(aa); 2020 c. 1, Sch. 5 para. 1(1)
2.3.By way of derogation from point 2.1, [F5the competent authority] may provide that supervised residue trials performed on their [F6constituent] 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 [F7on 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.U.K.
This derogation applies for supervised residue trials which actually started on or before 31 December 1997.
Textual Amendments
F5Words 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)
F6Word 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)
F7Words 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)
2.4.By way of derogation from point 2.1, for active substances consisting of micro-organisms or viruses, tests and analyses done to obtain data on the properties and/or safety with respect to other aspects than human health, may have been 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.]U.K.
Textual Amendments applied to the whole legislation
F1Repealed (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.
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