根據(jù)歐盟委員會第396/2005號法規(guī)第6章， ISK Biosciences Europe N.V.提交了該修訂申請。根據(jù)消費者暴露評估，歐洲食品安全局得出結(jié)論，美國授權的氟啶蟲酰胺使用量不會導致消費者急性或慢性接觸超過毒理學參考值，因此不太可能對消費者健康構成風險。

 

　　部分原文報道如下：

 

　　In accordance with Article 6 of Regulation （EC ） No 396/2005, the applicant ISK Biosciences Europe N.V. submitted a request to the competent national authority in Finland to set an import tolerance for the active substance flonicamid in various crops and products of animal origin on the basis of the authorised use of flonicamid in the USA . The data submitted in support of the request were found to be sufficient to derive maximum residue level （MRL ） proposals for all crops under assessment. based on the results of the feeding studies and the updated animal burden calculations, no need for new MRL proposals on products of animal origin was identified. Adequate analytical methods for enforcement are available to control the residues of flonicamid in plant and animal matrices. EFSA updated the most recent consumer risk assessment for flonicamid and concluded that the authorised USA uses of flonicamid will not result in acute or chronic consumer exposure exceeding the toxicological reference values and, therefore, is unlikely to pose a risk to consumers' health.

 

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