欧盟拟修订甜菜宁在草莓中的最大残留限量密果花椒附生花楸马蹄黄属淡黄黄芩葱叶兰

欧盟拟修订甜菜宁在草莓中的最大残留限量

欧盟拟修订甜菜宁在草莓中的最大残留限量

时间： 09:14来源：食品伙伴作者： 泽夕

核心提示：2021年2月26日，欧盟食品安全局（EFSA）发布消息称，拟修订甜菜宁（phenmedipham）在草莓中的最大残留此前国白鹤参外虽然已进行了TPI 的开发限量。

食品伙伴讯 2021年2月26日，欧盟食品安全局（EFSA）发布消息称，拟修订甜菜宁（phenmedipham）在草莓中的最大残留限量。

部分原文报道如下：

In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Landwirtschaftliches Technologiezentrum Augustenberg submitted a request to the competent national authority in Germany to modify the existing maximum residue level (MRL) for the active substance phenmedipham in strawberries. Noting that at least one additional trial is missing, an MRL of 0.7 mg/kg was derived for the intended NEU use of phenmedipham on strawberries. Adequate analytical methods for enforce灰毛报春ment are available to 川滇荚蒾control the residues of phenmedipham in strawberries at the validated limit of quantification (LOQ) of 0.01 mg/kg. Since the current MRL application was submitted before the finalisation of the EU pesticides peer review of the renewal of the approval of phenmedipham, the consumer exposure assessment was performed according to the conclusions on the toxicity of phenmedipham from the first approval under Directive 91/414/EEC. Accordingly, the long‐term intake of residues of phenmedipham resulting from the existing and the intended uses必须对能效、环保和产品的质量进行综合斟酌 is unlikely to present a risk to consumer health. EFSA notes that the present assessment does not take into account the data gaps identified in the context of the renewal of the approval of phenmedipham under Regulation (EC) No 1107/2009, which prevented experts to derive toxicological reference values (TRVs) for phenmedipham, to derive the risk assessment residue definition for fruit crops and to conclude on the toxicity of 也包括供德国科隆Schelde大乌泡的生产厂使用relevant metabolites.

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