Requirement to provide existing maximum residue level applications in support of new active substance approval or renewal applicationsU.K.
This section has no associated Explanatory Memorandum
8.—(1) Sub-paragraph (2) applies where—
(a)on or after [IP completion day] an application is made—
(i)for approval of an active substance or the amendment of the conditions of such an approval in accordance with Article 7(1) or (1A) of Regulation (EC) No 1107/2009, or
(ii)for renewal of approval of an active substance in accordance with Article 15 of Regulation (EC) No 1107/2009, and
(b)before [IP completion day] a relevant application for a maximum residue level was made in accordance with Article 7 of Regulation (EC) No 396/2005 as it had effect immediately before [IP completion day] .
(2) Where this sub-paragraph applies, the obligation in Article 8(1)(g) of Regulation (EC) No 1107/2009 or Article 7(1)(i) of Regulation (EU) No 844/2012 (as the case may be) to provide a copy of a relevant application for a maximum residue level as referred to in Article 7 of Regulation (EC) No 396/2005 is to be read as including an obligation to provide a copy of the application described in sub-paragraph (1)(b).
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