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    歐盟批準(zhǔn)bixafen作為農(nóng)藥入市
    日期:2013-04-26  來源:食品伙伴網(wǎng)

        食品伙伴網(wǎng) 據(jù)歐盟網(wǎng)站消息,4月18日歐盟委員會發(fā)布(EU) No 350/2013法規(guī),批準(zhǔn)bixafen作為農(nóng)藥入市。歐盟提醒成員國,在使用時應(yīng)該注意bixafen及其代謝物對植物、動物、土壤、水體構(gòu)成的風(fēng)險。新法規(guī)將自公布20天后生效,從2013年10月1日起實(shí)施。

        部分原文報道如下:

        COMMISSION IMPLEMENTING REGULATION (EU) No 350/2013   of 17 April 2013

        approving the active substance bixafen, 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, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011

        (Text with EEA relevance)

        THE EUROPEAN COMMISSION,

        Having regard to the Treaty on the Functioning of the European Union,

        Having regard to Regulation (EC) No 1107/2009 of the European Parliament and of the Council of 21 October 2009 concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC ( 1 ), and in particular Article 13(2) and Article 78(2) thereof,

        Whereas:

        (1) In accordance with Article 80(1)(a) of Regulation (EC) No 1107/2009, Council Directive 91/414/EEC ( 2 ) is to apply, with respect to the procedure and the conditions for approval, to active substances for which a decision has been adopted in accordance with Article 6(3) of that Directive before 14 June 2011. For bixafen the conditions of Article 80(1)(a) of Regulation (EC) No 1107/2009 are fulfilled by Commission Decision 2009/700/EC ( 3 )。

        (2) In accordance with Article 6(2) of Directive 91/414/EEC the United Kingdom received on 8 October 2008 an application from Bayer CropScience for the inclusion of the active substance bixafen in Annex I to Directive 91/414/EEC. Decision 2009/700/EC confirmed that the dossier was 'complete' in the sense that it could be considered as satisfying, in principle, the data and information requirements of Annexes II and III to Directive 91/414/EEC.

        (3) For that active substance, the effects on human and animal health and the environment have been assessed, in accordance with the provisions of Article 6(2) and (4) of Directive 91/414/EEC, for the uses proposed by the applicant. The designated rapporteur Member State submitted a draft assessment report on 19 July 2011.

        原文鏈接:<http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2013:108:0009:0012:EN:PDF>

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