根據(jù)歐盟委員會(huì)第396/2005號(hào)法規(guī)第6章，Nisso Chemical Europe GmbH向希臘國(guó)家主管部門提交申請(qǐng)，要求制定環(huán)氟菌胺在啤酒花中的進(jìn)口限量。經(jīng)過(guò)評(píng)估，歐盟食品安全局得出結(jié)論，根據(jù)所報(bào)道的農(nóng)業(yè)實(shí)踐，短期和長(zhǎng)期攝入使用環(huán)氟菌胺而產(chǎn)生的殘留物不太可能對(duì)消費(fèi)者健康構(gòu)成風(fēng)險(xiǎn)?？紤]到EFSA在MRL審核期間提出的某些MRL提案需要進(jìn)一步的確認(rèn)性數(shù)據(jù)，因此該結(jié)論應(yīng)被視為指示性的。部分原文報(bào)道如下：

 

　　In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Nisso Chemical Europe GmbH submitted a request to the competent national authority in Greece to set an import tolerance for the active substance cyflufenamid in hops. The data submitted in support of the request were found to be sufficient to derive an maximum residue level (MRL) proposal for hops; however, further risk management considerations are required to decide on the appropriate MRL values considering that the MRL in the country of origin is lower than the MRL proposal derived from the residue trials. Adequate analytical methods for enforcement are available to control the residues of cyflufenamid in the crop under consideration at the validated limit of quantification (LOQ) of 0.01 mg/kg. based on the consumer risk assessment results, EFSA concluded that the short‐term and long‐term intake of residues resulting from the use of cyflufenamid according to the reported agricultural practice in the country of origin is unlikely to present a risk to consumer health. This conclusion shall be regarded as indicative considering that some MRL proposals derived by EFSA during the MRL review require further confirmatory data.

 

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