...
首页> 外文期刊>EFSA Journal >Reasoned opinion on the modification of the existing MRLs for dicamba in herbs and herbal infusions (leaves and flowers)
【24h】

Reasoned opinion on the modification of the existing MRLs for dicamba in herbs and herbal infusions (leaves and flowers)

机译:关于修改现有中草药和中草药浸剂(叶和花)中麦草畏最大残留限量的合理意见

获取原文
           

摘要

In accordance with Article 6 of Regulation (EC) No 396/2005, France, hereafter referred to as the evaluating Member State (EMS), received an application from Syngenta Agro S.A.S. to modify the existing MRLs for the active substance dicamba in herbs and herbal infusions (leaves and flowers). In order to accommodate for the intended uses of dicamba, France proposed to raise the default MRL from the limit of quantification of 0.05* mg/kg to 4 mg/kg in herbs and 40 mg/kg in herbal infusions (leaves and flowers). France drafted an evaluation report in accordance with Article 8 of Regulation (EC) No 396/2005, which was submitted to the European Commission and forwarded to EFSA. EFSA concludes that the data are sufficient to derive a MRL proposal of 4 mg/kg for herbs. For herbal infusions (leaves) a MRL proposal of 40 mg/kg is derived by extrapolation from the residue trials conducted on oregano, considering a default dehydration factor of 10. Taking into account that the nature of the other crops classified in this group (hibiscus flowers, rose petals, jasmine flowers, elderflowers and lime) is not comparable, and that the notified GAP seems to be inappropriate for these crops, no MRL proposal is made for herbal infusions (flowers). A validated analytical enforcement method was submitted to control residues of dicamba in fresh herbs. For herbal infusions, a matrix which is considered as difficult to analyse, specific validation data should be provided. However, taking into account the successful validation in different matrix types, the analytical method is accepted on a provisional basis also for herbal infusion. Based on the risk assessment results, EFSA concludes that the proposed use of dicamba on herbs and herbal infusions (leaves) will not result in a consumer exposure exceeding the toxicological reference values and therefore is unlikely to pose a consumer health risk.
机译:根据(EC)396/2005号条例第6条,法国(以下简称为评估成员国(EMS))收到先正达Agro S.A.S.的申请。修改草药和草药浸液(叶子和花朵)中麦草畏的现有最大残留限量。为了适应麦草畏的预期用途,法国建议将默认的最大残留限量从草药的定量限(0.05 * mg / kg)提高到4 mg / kg,草药浸出液(叶和花)的40 mg / kg。法国根据(EC)第396/2005号条例第8条起草了一份评估报告,该评估报告已提交给欧洲委员会并转发给EFSA。欧洲食品安全局(EFSA)得出结论,该数据足以得出草药的最大残留限量建议为4 mg / kg。对于草药浸剂(叶),从牛至的残留试验中推算得出最大残留限量为40 mg / kg,考虑默认脱水因子为10。考虑到该类别中其他农作物的性质(芙蓉)花,玫瑰花瓣,茉莉花,接骨木花和酸橙)不可比,并且通知的GAP似乎不适用于这些农作物,没有针对草药注入(花)制定MRL提案。提交了经过验证的分析实施方法来控制新鲜药材中麦草畏的残留量。对于草药输液,应提供难以分析的基质,应提供具体的验证数据。但是,考虑到在不同基质类型中的成功验证,该分析方法也可以临时用于草药输液。根据风险评估结果,欧洲食品安全局(EFSA)得出结论,拟在麦草和草药浸液(叶)中使用麦草畏的提议使用不会导致消费者暴露超过毒理学参考值,因此不太可能构成消费者健康风险。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号