據歐盟官方公報消息，2019年1月30日，歐盟委員會發布（EU）2019/139號條例，批準球孢白僵菌株IMI389521作為植物保護產品投放市場，并修訂實施細則（EU）No 540/2011的附件II。
據了解，球孢白僵菌株IMI389521的最大水平為0.09 mg/kg，批準使用期限為2019年2月19日至2029年2月19日。
部分原文報道如下：
In accordance with Article 7（1） of Regulation （EC） No 1107/2009 the Netherlands received on 28 October 2014 an application from Exosect Limited for the approval of the active substance Beauveria bassiana strain IMI389521.
In accordance with Article 9（3） of Regulation （EC） No 1107/2009, the Netherlands, as rapporteur Member State, notified the applicant, the other Member States, the Commission and the European Food Safety Authority （‘the Authority’） on 2 June 2015 of the admissibility of the application.
On 22 February 2016 the rapporteur Member State submitted a draft assessment report to the Commission with a copy to the Authority, assessing whether that active substance can be expected to meet the approval criteria provided for in Article 4 of Regulation （EC） No 1107/2009.
The Authority complied with Article 12（1） of Regulation （EC） No 1107/2009. In accordance with Article 12（3） of Regulation （EC） No 1107/2009, it requested that the applicant supply additional information to the Member States, the Commission and the Authority. The assessment of the additional information by the rapporteur Member State was submitted to the Authority in the format of an updated draft assessment report on 2 February 2017.
本文由食品伙伴網食品資訊中心編輯，供網友參考，歡迎轉載，轉載請注明出處！有任何疑問，請聯系news@foodmate.net。
日期：2019-01-31
據了解，球孢白僵菌株IMI389521的最大水平為0.09 mg/kg，批準使用期限為2019年2月19日至2029年2月19日。
部分原文報道如下：
In accordance with Article 7（1） of Regulation （EC） No 1107/2009 the Netherlands received on 28 October 2014 an application from Exosect Limited for the approval of the active substance Beauveria bassiana strain IMI389521.
In accordance with Article 9（3） of Regulation （EC） No 1107/2009, the Netherlands, as rapporteur Member State, notified the applicant, the other Member States, the Commission and the European Food Safety Authority （‘the Authority’） on 2 June 2015 of the admissibility of the application.
On 22 February 2016 the rapporteur Member State submitted a draft assessment report to the Commission with a copy to the Authority, assessing whether that active substance can be expected to meet the approval criteria provided for in Article 4 of Regulation （EC） No 1107/2009.
The Authority complied with Article 12（1） of Regulation （EC） No 1107/2009. In accordance with Article 12（3） of Regulation （EC） No 1107/2009, it requested that the applicant supply additional information to the Member States, the Commission and the Authority. The assessment of the additional information by the rapporteur Member State was submitted to the Authority in the format of an updated draft assessment report on 2 February 2017.
本文由食品伙伴網食品資訊中心編輯，供網友參考，歡迎轉載，轉載請注明出處！有任何疑問，請聯系news@foodmate.net。
日期：2019-01-31
