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本文引用的文献

1
Guidance for the identification of endocrine disruptors in the context of Regulations (EU) No 528/2012 and (EC) No 1107/2009.关于在(欧盟)第528/2012号法规和(欧盟)第1107/2009号法规背景下识别内分泌干扰物的指南。
EFSA J. 2018 Jun 7;16(6):e05311. doi: 10.2903/j.efsa.2018.5311. eCollection 2018 Jun.
2
Use of EFSA Pesticide Residue Intake Model (EFSA PRIMo revision 3).使用欧洲食品安全局农药残留摄入模型(EFSA PRIMo第3版修订本)。
EFSA J. 2018 Jan 15;16(1):e05147. doi: 10.2903/j.efsa.2018.5147. eCollection 2018 Jan.
3
Clarification of some aspects related to genotoxicity assessment.关于遗传毒性评估相关某些方面的阐释
EFSA J. 2017 Dec 18;15(12):e05113. doi: 10.2903/j.efsa.2017.5113. eCollection 2017 Dec.

三唑锡和三环锡最大残留限量的针对性审查。

Targeted review of maximum residue levels (MRLs) for azocyclotin and cyhexatin.

作者信息

Bellisai Giulia, Bernasconi Giovanni, Binaglia Marco, Brancato Alba, Carrasco Cabrera Luis, Castellan Irene, Castoldi Anna Federica, Chiusolo Arianna, Crivellente Federica, Del Aguila Monica, Ferreira Lucien, Santonja German Giner, Greco Luna, Istace Frederique, Jarrah Samira, Lanzoni Anna, Leuschner Renata, Mangas Iris, Miron Ileana, Nave Stefanie, Panzarea Martina, Parra Morte Juan Manuel, Pedersen Ragnor, Reich Hermine, Ruocco Silvia, Santos Miguel, Scarlato Alessia Pia, Terron Andrea, Theobald Anne, Tiramani Manuela, Verani Alessia

出版信息

EFSA J. 2023 Jun 9;21(6):e08038. doi: 10.2903/j.efsa.2023.8038. eCollection 2023 Jun.

DOI:10.2903/j.efsa.2023.8038
PMID:37304356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10251540/
Abstract

In accordance with Article 43 of Regulation (EC) 396/2005, EFSA received a request from the European Commission to review the existing maximum residue levels (MRLs) for the non-approved active substances azocyclotin and cyhexatin in view of the possible lowering of these MRLs. EFSA investigated the origin of the current EU MRLs. For existing EU MRLs that reflect previously authorised uses in the EU, or that are based on obsolete Codex Maximum Residue Limits, or import tolerances that are not required any longer, EFSA proposed the lowering to the limit of quantification. EFSA performed an indicative chronic and acute dietary risk assessment for the revised list of MRLs to allow risk managers to take the appropriate decisions. For some commodities under assessment, further risk management discussions are required to decide which of the risk management options proposed by EFSA should be implemented in the EU MRL legislation.

摘要

根据欧盟法规(EC)396/2005第43条,欧洲食品安全局(EFSA)收到欧盟委员会的请求,要求鉴于可能降低非批准活性物质唑环锡和三环锡的现有最大残留限量(MRLs),对其进行审查。EFSA调查了当前欧盟MRLs的来源。对于反映欧盟先前批准用途的现有欧盟MRLs,或基于过时的食品法典最大残留限量,或不再需要的进口容忍度,EFSA提议将其降低到定量限。EFSA对修订后的MRLs清单进行了指示性慢性和急性膳食风险评估,以便风险管理者做出适当决策。对于一些正在评估的商品,需要进一步进行风险管理讨论,以决定应在欧盟MRL立法中实施EFSA提议的哪些风险管理选项。