食品伙伴網(wǎng)訊  2019年8月29日，歐盟食品安全局（EFSA）就審查?，斁兀‥mamectin）的最大殘留限量發(fā)布意見(jiàn)。

 

　　根據(jù)歐盟（EC）No 396/2005的第12章的規(guī)定，歐盟食品安全局審查了?，斁氐淖畲髿埩粝蘖?。經(jīng)過(guò)評(píng)估歐盟食品安全局認(rèn)為，由于部分?jǐn)?shù)據(jù)的缺少，消費(fèi)者可能面臨嚴(yán)重風(fēng)險(xiǎn)。消費(fèi)者風(fēng)險(xiǎn)評(píng)估僅被認(rèn)為是指示性的，所以EFSA提出的某些最大殘留限量需要進(jìn)一步的評(píng)估。

 

　　部分原文報(bào)道如下：

 

　　According to Article 12 of Regulation （EC） No 396/2005, EFSA has reviewed the maximum residue levels （MRLs） currently established at European level for the pesticide active substance emamectin. To assess the occurrence of emamectin residues in plants, processed commodities, rotational crops and livestock, EFSA considered the conclusions derived in the framework of Regulation （EC） No 1107/2009, the MRLs established by the Codex Alimentarius Commission as well as the European authorisations reported by Member States （including the supporting residues data）。 based on the assessment of the available data, MRL proposals were derived and a consumer risk assessment was carried out. Some information required by the regulatory framework was missing and a possible acute risk to consumers was identified. Hence, the consumer risk assessment is considered indicative only, some MRL proposals derived by EFSA still require further consideration by risk managers and measures for reduction of the consumer exposure should also be considered.

 

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