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The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019

Draft Legislation:

This is a draft item of legislation and has not yet been made as a UK Statutory Instrument. This draft has been replaced by a new draft, The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 ISBN 978-0-11-118153-9

Plant Protection Products (Fees and Charges) Regulations 2011

This section has no associated Explanatory Memorandum

14.—(1) Schedule 1 is amended as follows.

(2) In paragraph 1—

(a)in the table—

(i)in item 4 in the second column, after “application(2)” omit “(3)”;

(ii)omit items 5, 5a and 5b;

(iii)in item 11 in the second column, for “for lead zonal re-registration and new product applications” substitute “to discuss potential product applications”;

(iv)omit item 12;

(b)in the notes following the table—

(i)omit notes (3), (5) and (6);

(ii)in note (7) for “items 1-5, 10, 11 and 12” substitute “items 1-4, 10 and 11”;

(iii)in note (16) omit “to the United Kingdom to act as lead zonal rapporteur”;

(iv)omit note (17);

(v)in note (18) for “the United Kingdom” substitute “a United Kingdom competent authority”.

(3) In paragraph 2—

(a)in the heading, for “or synergist” substitute “, synergist or basic substance”;

(b)in the first sentence, for “or synergist” substitute “, synergist or basic substance”;

(c)in the table—

(i)in the heading before item 1, for “or synergist” substitute “, synergist or basic substance”;

(ii)omit item 2;

(iii)in item 3 for the words in the second column substitute “Co-ordination of scientific advice and public consultation and finalising the draft assessment report”;

(iv)in items 7 and 10, for the words in the second column substitute “Co-ordination of scientific advice and public consultation, and finalising the draft assessment report”;

(v)in item 12, in the second column, after “synergist,” insert “basic substance,”;

(d)in the notes following the table—

(i)omit note (2);

(ii)in note (3)—

(aa)at the beginning insert “In relation to active substances, safeners or synergists,”;

(bb)after the first sentence insert “In relation to basic substances, a full data package comprises the complete dossier (the information referred to in Article 23(3) of Regulation 1107/2009) to support one or more uses of the basic substance.”;

(cc)in the second sentence after “the product” insert “or basic substance”;

(iii)in note (4)—

(aa)omit paragraph (c);

(bb)in paragraph (d) at the beginning insert “in relation to active substances, safeners or synergists,”;

(cc)omit paragraph (e);

(dd)in paragraphs (f) and (g), at the beginning insert “in relation to active substances, safeners or synergists,”;

(ee)after paragraph (g) insert—

(h)in relation to basic substances, resubmissions (for example where the previous application for approval under Regulation 1107/2009 has been unsuccessful and a new application is made in an attempt to address all the concerns raised from that earlier submission);

(i)in relation to basic substances, data to support a change to the conditions of approval of the basic substance.;

(iv)for the final sentence substitute—

The evaluation of scientific peer reviewed open literature on the active substance or basic substance and its relevant metabolites will be treated as a partial data package.

(4) Omit paragraph 4 (including the table, and the notes following the table, in that paragraph).

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