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首页> 外文期刊>EFSA Journal >Scientific opinion on an application for renewal of authorisation for continued marketing of maize?1507 and derived food and feed submitted under Articles 11 and 23 of Regulation (EC) No?1829/2003 by Pioneer Overseas Corporation and Dow AgroSciences LLC
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Scientific opinion on an application for renewal of authorisation for continued marketing of maize?1507 and derived food and feed submitted under Articles 11 and 23 of Regulation (EC) No?1829/2003 by Pioneer Overseas Corporation and Dow AgroSciences LLC

机译:Pioneer Overseas Corporation和Dow AgroSciences LLC根据第(EC)1829/2003号法规第11和23条提交的关于继续销售玉米1507和衍生食品和饲料的授权续签的科学意见

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摘要

Following the submission of application EFSA‐GMO‐RX‐001 under Regulation (EC) No 1829/2003 from Pioneer Overseas Corporation and Dow Agrosciences LLC, the Panel on Genetically Modified Organisms of the European Food Safety Authority (GMO Panel) was asked to deliver a scientific risk assessment on the data submitted in the frame of a renewal of authorisation application of the insect‐resistant and herbicide‐tolerant genetically modified (GM) maize 1507. The data package received in the frame of this renewal application contained post‐market environmental monitoring reports, a systematic search and evaluation of literature, an updated bioinformatics analysis and additional documents or studies performed by or on behalf of the applicant. The GMO Panel assessed this data package for possible new hazards, modified exposure or new scientific uncertainties identified during the authorisation period and not previously assessed in the frame of the original application. Under the assumption that the DNA sequence of the event in maize 1507 considered for renewal is identical to the corrected sequence of the originally assessed event, the GMO Panel concludes that no new hazards or modified exposure and no new scientific uncertainties were identified for the application for renewal that would change the conclusions of the original risk assessment on maize 1507 (EFSA, 2005b, 2009).
机译:根据Pioneer Overseas Corporation和Dow Agrosciences LLC根据法规(EC)1829/2003提交的EFSA-GMO-RX-001申请后,欧洲食品安全局转基因生物小组(GMO小组)被要求提供对在抗虫和耐除草剂的转基因玉米(GM)1503的授权申请书续展中提交的数据进行科学的风险评估。在此续展申请书中收到的数据包包含上市后环境监测报告,系统地搜索和评估文献,更新的生物信息学分析以及由申请人或代表申请人进行的其他文件或研究。 GMO小组评估了此数据包,以了解授权期内发现的,先前未在原始申请框架中进行过评估的可能的新危害,暴露量变化或新的科学不确定性。假设考虑更新的玉米1507中该事件的DNA序列与原先评估的事件的更正序列相同,那么GMO小组得出结论认为,该玉米的申请没有新的危害或暴露改变,也没有发现新的科学不确定性。进行更新,这将改变对玉米1507的原始风险评估的结论(欧洲食品安全局,2005b,2009)。

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