根據歐盟委員會第396/2005號法規(guī)第12章，歐盟食品安全局審查了纈菌胺的最大殘留限量。盡管沒有發(fā)現纈菌胺對消費者有明顯的風險，但缺少監(jiān)管框架要求的某些信息。因此，消費者風險評估僅被認為是指示性的，EFSA提出的一些MRL建議仍需風險管理者進一步考慮。部分原文報道如下：

 

　　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 valifenalate. To assess the occurrence of valifenalate residues in plants, processed commodities, rotational crops and livestock, EFSA considered the conclusions derived in the framework of Commission Regulation (EU) No 188/2011, as well as European authorisations reported by Member States and the UK (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. Although no apparent risk to consumers was identified, some information required by the regulatory framework was missing. Hence, the consumer risk assessment is considered indicative only and one MRL proposal derived by EFSA still requires further consideration by risk managers.

 

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