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2022年1月13日,，歐盟食品安全局（EFSA）就審查敵草胺（novaluron）的現(xiàn)有最大殘留水平發(fā)布意見,。

根據(jù)歐盟委員會(huì)第396/2005號(hào)法規(guī)第12章，歐盟食品安全局審查了敵草胺的最大殘留限量。根據(jù)對(duì)現(xiàn)有數(shù)據(jù)的評(píng)估,，得出了毒理學(xué)參考值，并對(duì)現(xiàn)有的最大殘留限量和進(jìn)口容限進(jìn)行了消費(fèi)者風(fēng)險(xiǎn)評(píng)估,。發(fā)現(xiàn)所有最大殘留限量和進(jìn)口公差都沒(méi)有充分的數(shù)據(jù)支持,，并確定了對(duì)消費(fèi)者的可能長(zhǎng)期風(fēng)險(xiǎn)。因此,，風(fēng)險(xiǎn)管理者需要進(jìn)一步考慮,。

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. Although this active substance is not authorised within the European Union, MRLs were established by the Codex Alimentarius Commission (codex maximum residue limits; CXLs) and import tolerances were reported by Member States and the UK (including the supporting residues data). Considering that no toxicological reference values are currently established in Europe for novaluron because the peer review for the approval was terminated before an EFSA conclusion was issued, the toxicological profile of novaluron was also assessed, in order to be able to perform the consumer risk assessment in the framework of the art 12 MRL review. based on the assessment of the available data, toxicological reference values were derived, and a consumer risk assessment was carried out for the existing CXLs and import tolerances. All CXLs and import tolerances were found to be supported by inadequate data and a possible chronic risk to consumers was identified. Hence, further consideration by risk managers is needed.

更多詳情參見：https://efsa.onlinelibrary.wiley.com/doi/10.2903/j.efsa.2022.7041