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活性物质肟菌酯(评估变体为肟菌酯乙酯)农药风险评估的更新同行评审

Updated peer review of the pesticide risk assessment of the active substance trinexapac (variant evaluated trinexapac-ethyl).

作者信息

Alvarez Fernando, Arena Maria, Auteri Domenica, Binaglia Marco, Castoldi Anna Federica, Chiusolo Arianna, Colagiorgi Angelo, Colas Mathilde, Crivellente Federica, De Lentdecker Chloe, De Magistris Isabella, Egsmose Mark, Fait Gabriella, Ferilli Franco, Gouliarmou Varvara, Halling Katrin, Nogareda Laia Herrero, Ippolito Alessio, Istace Frederique, Jarrah Samira, Kardassi Dimitra, Kienzler Aude, Lanzoni Anna, Lava Roberto, Leuschner Renata, Linguadoca Alberto, Lythgo Christopher, Magrans Oriol, Mangas Iris, Miron Ileana, Molnar Tunde, Padovani Laura, Padricello Vincenzo, Panzarea Martina, Parra Morte Juan Manuel, Rizzuto Simone, Rortais Agnès, Serafimova Rositsa, Sharp Rachel, Szentes Csaba, Szoradi Andras, Terron Andrea, Theobald Anne, Tiramani Manuela, Vianello Giorgia, Villamar-Bouza Laura

出版信息

EFSA J. 2023 Jun 28;21(6):e08082. doi: 10.2903/j.efsa.2023.8082. eCollection 2023 Jun.

Abstract

The conclusions of the European Food Safety Authority (EFSA) following the peer review of the initial risk assessments carried out by the competent authorities of the rapporteur Member State, Lithuania, and co-rapporteur Member State, Latvia, for the pesticide active substance trinexapac and the assessment of applications for maximum residue levels (MRLs) are reported. The context of the peer review was that required by Commission Implementing Regulation (EU) No 844/2012. The conclusions were reached on the basis of the evaluation of the representative use of trinexapac as a plant growth regulator on barley (winter and spring) and wheat (winter). MRLs were assessed in rye. The conclusions were updated with regard to the endocrine-disrupting properties following a mandate received from the European Commission in January 2019.The reliable end points, appropriate for use in regulatory risk assessment and the proposed MRLs, are presented. The confirmatory data following the review of existing MRLs according to Article 12 of Regulation (EC) No 396/2005 were also assessed under this conclusion. Missing information identified as being required by the regulatory framework is listed. Concerns are reported where identified.

摘要

报告了欧洲食品安全局(EFSA)在对报告成员国立陶宛和联合报告成员国拉脱维亚的主管当局针对农药活性物质调环酸进行的初步风险评估以及最大残留限量(MRL)申请评估开展同行评审之后得出的结论。同行评审的背景是委员会实施条例(欧盟)第844/2012号所要求的。这些结论是在评估调环酸作为植物生长调节剂在大麦(冬大麦和春大麦)和小麦(冬小麦)上的代表性用途的基础上得出的。对黑麦中的最大残留限量进行了评估。根据2019年1月从欧盟委员会收到的一项任务授权,对内分泌干扰特性方面的结论进行了更新。列出了适用于监管风险评估的可靠终点以及提议的最大残留限量。根据第(EC)396/2005号条例第12条对现有最大残留限量进行审查后的确认数据也在此结论下进行了评估。列出了监管框架要求的但发现缺失的信息。报告了已识别出的问题。

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