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欧盟国家食品安全局拟修定敌菜宁(phenmedipham)在|nba买球官网

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    本文摘要:nba买球官方网站,nba买球官网,一部分全文报导以下:InaccordancewithArticle6ofRegulation(EC)No396/2005,theapplicantUPLEuropeLtd.submittedanapplicationtothecompetentnationalauthorityinGermany(evaluatingMemberState,EMS)toraisetheexistingmaximumresiduelevel(MRL)to0.15mg/kgfortheactivesubstancephenmediphaminceleriac.ThesubmittedresiduetrialsaresufficienttoderiveatentativeMRLof0.15mg/kg,pendingfurtherinvestigationofnatureofphenmediphamresiduesinrootcrops.ForthisassessmentEFSAconsideredthattheavailablesugarbeetmetabolismdatacanbeextrapolatedtoceleriaconatentativebasis.Theacceptabilityofsuchproposalshallbefurtherconsideredbyriskmanagers.Adequateanalyticalmethodsforenforcementareavailabletocontroltheresiduesofphenmediphaminceleriacatthevalidatedlimitofquantification(LOQ)of0.01mg/kg.SincethecurrentMRLapplicationwassubmittedbeforethefinalisationoftheEUpesticidespeerreviewoftherenewaloftheapprovalofphenmedipham,theconsumerexposureassessmentwasperformedaccordingtotheconclusionsonthetoxicityofphenmediphamfromthefirstapprovalunderDirective91/414/EEC.Accordingly,thelong‐termintakeofresiduesofphenmediphamresultingfromtheexistingandtheintendedusesdoesnotindicatearisktoconsumerhealth.ThepresentassessmentdoesnotconsiderthedatagapsidentifiedinthecontextoftherenewaloftheapprovalofphenmediphamunderRegulation(EC)No1107/2009whichpreventedexpertstoderivetoxicologicalreferencevalues(TRVs)forphenmedipham,toderivetheriskassessmentresiduedefinitionforrootcropsotherthansugarbeetandtoconcludeonthetoxicityofrelevantmetabolites.有一切疑惑,请联络。

    限量

    2021年3月22日,欧盟国家食品安全局(EFSA)公布信息称,拟修定敌菜宁(phenmedipham)在块根芹中的较大 残留限量。依据欧盟国家规章(EC)No396/2005第六章的要求,UPLEuropeLtd.递交了该修定申请办理。现阶段敌菜宁在块根芹中目前的较大 残留限量为0.01mg/kg,拟议的较大 残留限量为0.15mg/kg(必须进一步的风险管控考虑到)。

    根芹

    一部分全文报导以下:InaccordancewithArticle6ofRegulation(EC)No396/2005,theapplicantUPLEuropeLtd.submittedanapplicationtothecompetentnationalauthorityinGermany(evaluatingMemberState,EMS)toraisetheexistingmaximumresiduelevel(MRL)to0.15mg/kgfortheactivesubstancephenmediphaminceleriac.ThesubmittedresiduetrialsaresufficienttoderiveatentativeMRLof0.15mg/kg,pendingfurtherinvestigationofnatureofphenmediphamresiduesinrootcrops.ForthisassessmentEFSAconsideredthattheavailablesugarbeetmetabolismdatacanbeextrapolatedtoceleriaconatentativebasis.Theacceptabilityofsuchproposalshallbefurtherconsideredbyriskmanagers.Adequateanalyticalmethodsforenforcementareavailabletocontroltheresiduesofphenmediphaminceleriacatthevalidatedlimitofquantification(LOQ)of0.01mg/kg.SincethecurrentMRLapplicationwassubmittedbeforethefinalisationoftheEUpesticidespeerreviewoftherenewaloftheapprovalofphenmedipham,theconsumerexposureassessmentwasperformedaccordingtotheconclusionsonthetoxicityofphenmediphamfromthefirstapprovalunderDirective91/414/EEC.Accordingly,thelong‐termintakeofresiduesofphenmediphamresultingfromtheexistingandtheintendedusesdoesnotindicatearisktoconsumerhealth.ThepresentassessmentdoesnotconsiderthedatagapsidentifiedinthecontextoftherenewaloftheapprovalofphenmediphamunderRegulation(EC)No1107/2009whichpreventedexpertstoderivetoxicologicalreferencevalues(TRVs)forphenmedipham,toderivetheriskassessmentresiduedefinitionforrootcropsotherthansugarbeetandtoconcludeonthetoxicityofrelevantmetabolites.有一切疑惑,请联络。


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