Revision of the review of the existing maximum residue levels for the active substance lambda‐cyhalothrin
2015; Wiley; Volume: 13; Issue: 12 Linguagem: Inglês
10.2903/j.efsa.2015.4324
ISSN1831-4732
Tópico(s)Effects and risks of endocrine disrupting chemicals
ResumoEFSA JournalVolume 13, Issue 12 4324 Reasoned OpinionOpen Access Revision of the review of the existing maximum residue levels for the active substance lambda-cyhalothrin European Food Safety Authority (EFSA), European Food Safety Authority (EFSA)Search for more papers by this author European Food Safety Authority (EFSA), European Food Safety Authority (EFSA)Search for more papers by this author First published: 02 December 2015 https://doi.org/10.2903/j.efsa.2015.4324Citations: 6 Correspondence: pesticides.mrl@efsa.europa.eu Acknowledgement: EFSA wishes to thank the rapporteur Member State Sweden for the preparatory work on this scientific output. Approval date: 26 November 2015 Published date: 2 December 2015 Question number: EFSA-Q-2015-00058 On request from: European Commission Amended: 16 May 2018 AboutPDF ToolsExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat Abstract In compliance with Article 43 of Regulation (EC) No 396/2005, the European Food Safety Authority (EFSA) received from the European Commission a mandate to update its previous review of the existing maximum residue levels (MRLs) for lambda-cyhalothrin on the basis of the new toxicological reference values and of the new evaluation report presented by Italy. Based on the assessment of the available data, MRL proposals were derived and a consumer risk assessment was carried out. Some information required by the regulatory framework was missing and possible chronic and acute risk to consumers was identified. Hence, the consumer risk assessment is considered indicative only, all MRL proposals derived by EFSA still require further consideration by risk managers and measures for reduction of the consumer exposure should also be considered. References Austria, 2015. 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