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    當(dāng)前位置: 首頁 » 食品資訊 » 外訊導(dǎo)讀 » 歐盟就活性物質(zhì)醚菌胺的農(nóng)藥風(fēng)險(xiǎn)評估發(fā)布同行評審

    歐盟就活性物質(zhì)醚菌胺的農(nóng)藥風(fēng)險(xiǎn)評估發(fā)布同行評審

    放大字體  縮小字體 時(shí)間:2023-11-01 11:27 來源:食品伙伴網(wǎng) 作者: 澤夕   
    核心提示:據(jù)歐盟食品安全局(EFSA )消息,2023年10月30日,歐盟食品安全局就活性物質(zhì)醚菌胺(dimoxystrobin)的農(nóng)藥風(fēng)險(xiǎn)評估發(fā)布同行評審。
       食品伙伴網(wǎng)訊  據(jù)歐盟食品安全局EFSA )消息,2023年10月30日,歐盟食品安全局就活性物質(zhì)醚菌胺(dimoxystrobin)的農(nóng)藥風(fēng)險(xiǎn)評估發(fā)布同行評審。
     
      經(jīng)過評估,將醚菌胺作為殺菌劑用在油菜和向日葵的基礎(chǔ)上,歐盟食品安全局提出了適用于監(jiān)管風(fēng)險(xiǎn)評估和建議的最大殘留限量的可靠端點(diǎn),列出了監(jiān)管框架要求的缺失信息,在確定的地方提出問題。部分原文報(bào)道如下:
     
      The conclusions of the EFSA following the peer review of the initial risk assessments carried out by the competent authorities of the rapporteur Member State, Hungary, and co-rapporteur Member State, Ireland, for the pesticide active substance dimoxystrobin as well as the assessment of maximum residue levels (MRLs) and confirmatory data following the review of the existing MRLs of dimoxystrobin according to Article 12 of Regulation (EC) No 396/2005 are reported. The context of the peer review was that required by Commission Implementing Regulation (EU) No 844/2012. In June 2023, the European Commission sent a mandate confirming the need to adopt and publish a conclusion on the peer review of the pesticide risk assessment of the active substance dimoxystrobin excluding the full assessment of endocrine-disrupting properties, containing all the results of the peer review process related to the renewal of approval as well as the assessment of the application for MRL for oilseed rapeseed, poppy seed, mustard seed and gold of pleasure seed, and the MRL application addressing the confirmatory data identified during the MRL review under Article 12 of Regulation (EC) No 396/2005. The conclusions were reached on the basis of the evaluation of the representative uses of dimoxystrobin as a fungicide on oilseed rape and sunflower. MRLs were assessed in rapeseeds, poppy seed, mustard seed and Gold of pleasure seed. The reliable end points, appropriate for use in regulatory risk assessment and the proposed MRLs, are presented. Missing information identified as being required by the regulatory framework is listed. Concerns are presented where identified.
     
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    日期:2023-11-01
     
     
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