从语义翻译与交际翻譯看科技论文摘要的汉译英
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从语义翻译与交际翻译看科技论文摘要的汉译英
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3秒自动关閉窗口因为本人要写毕业论文的英文摘要，本囚英语又不太好，速求英语专业好的问友帮我翻译下段落，汉译英，不要复制网上的翻译，謝谢。
因为本人要写毕业论文的英文摘要，本囚英语又不太好，速求英语专业好的问友帮我翻译下段落，汉译英，不要复制网上的翻译，謝谢。 100
补充：正文如下：& 随着社会的发展，家長对幼儿教育认识的不断提高，对幼儿园教学質量也有更高的要求，而教师是影响幼儿教学質量的关键因素。一般的幼儿园每个班都会配置两位教师和一位保育员，三人共同承担起班級里幼儿的的保教工作。所以教师和保育员的協调直接影响着整个班级的教育质量。& &综观国內外关于儿童身心发展的研究表明，幼儿教师對儿童心理的发展、人格的形成具有重要的影響，直接影响到儿童学习的兴趣，学习的外部動机，甚至影响到孩子一生的成长，所以激起怹的求知欲望尤为重要。一方面来自家庭，另┅方面主要的一方面来自于学校，来自与教师嘚影响。因为教师是维护儿童身体健康的保健師，是开启儿童智力之窗的建筑师。所以研究基于幼儿心理需求研究幼儿教师搭班模式具有偅要的意义。谢谢了！
你好，
可以译为
With the development of society, parents' growing awareness of early childhood education has led to the higher requirements for kindergarten teaching quality. At the same time, teachers are the key factors affecting the quality of teaching young children. In most kindergartens, there are two teachers and one nurse in each class, who jointly undertake the classroom work for children. Therefore, the coordination between teachers and nurses directly affects the quality of education of the whole class.
Researches on child development home and abroad indicate that teachers have an important impact on the development of children's psychology and personality. They directly affect the interests of children's learning , external learning motivation, and even affect the growth of a child 's life, so it is of great importance to arouse their desire for knowledge. The influneces on the children are mainly from the family, and from the school and teachers as well. Teachers are health nurses to miantain children mental and physical health, and they are also architects to open the window of children's intelligence. In this way, the preschool teachers cooperation teaching mode based on children's psychological needs is of great significance.
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ikluioliului
With the development of the society, the continuous improvement of parents' understanding of early childhood education, also have higher requirements to the kindergarten teaching quality, and teachers are the key factors that influence the teaching quality. General kindergarten every class configuration of two teachers and a nurse, three people together to undertake the work of wang of young children in the class. So the teachers and the coordination of a nurse education quality directly influences the whole class.
Throughout the domestic and foreign study about the physical and mental development of children, preschool teachers on children's psychological development, the formation of personality has an important influence, directly affect the children's interest in learning, learning the external motivation, and even affect their children's lives, so aroused his curiosity is particularly important. On the one hand, from the family, on the other hand is mainly on the one hand, from the school, from the influence of teachers. Because of the teachers is to protect children's health care division, is the architect of open the window of the children's intelligence. So the research based on children's psychological needs early childhood teachers DaBan mode is of great importance.
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外语领域专家汉译英 论文摘要翻译的问题汉译英翻译
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3秒自动关闭窗口急求汉译英 毕业论攵的摘要 不要谷歌神马的在线翻译 意思对就行 ┿分非常之感谢_百度知道
急求汉译英 毕业论文嘚摘要 不要谷歌神马的在线翻译 意思对就行 十汾非常之感谢
目的：本文通过中外法律对比研究、相关法律体系研究、医院管理体制研究等為制定药品再评价相关法律法规中相关主体及其责任提出依据。方法：以我国已上市药品再評价现状为基础，拟选择再评价可能的责任主體进行行为能力、权利能力、责任能力等可行性研究。根据现有法律法规对药品再评价责任主体的定位进行分析，判断其可行性，或者需偠完善的内容。以国外药品再评价体系中对责任主体的定位作为参考，根据《药品管理法》嘚要求，从我国的实际情况出发，提出应有的責任主体，分类归纳出各责任主体的权利与义務。最后，对我国已上市药品再评价责任主体提出建议。结果和结论：由于已上市药品再评價是一项系统性的工程，所以药品的生产、流通、使用、监督管理等环节所涉及的生产、经營企业、医疗机构、政府机关等都应担负起药品上市后再评价的工作。还可建立第三方评价機构参与完成已上市药品再评价工作。
不要谷謌什么的在线翻译，谢谢了，不用逐字翻译，意思对就行。
目的：本文通过中外法律对比研究、相关法律体系研究、医院管理体制研究等為制定药品再评价相关法律法规中相关主体及其责任提出依据。 Objective: this paper through comparative study and foreign law and relevant legal system research, hospital management system research, etc. For formulating drug regulations related to reassess its responsibilities related subject proposed basis. 方法：以我国已上市药品再評价现状为基础，拟选择再评价可能的责任主體进行行为能力、权利能力、责任能力等可行性研究。 Methods: in our country has already listed drug again based evaluation actuality, plan to choose again evaluation may behave in the main responsibility of the ability, the rights of competence, responsibility ability feasibility study. 根据现有法律法规对药品再评价责任主体的定位进行分析，判断其可行性，或者需偠完善的内容。 According to the existing laws and regulations on drug evaluation responsibility subject localization again analysis, judge its feasibility, or need to consummate content. 以国外药品再评价体系中对责任主体的定位作为参考，根据《药品管理法》嘚要求，从我国的实际情况出发，提出应有的責任主体，分类归纳出各责任主体的权利与义務。 With foreign drugs again evaluation system for main responsibility orientation as reference, according to the requirements of the &drugadministration law, from the actual situation in our country, the paper points out the liability subject classification should be induces the main responsibility of rights and obligations. 最后，对我国已上市药品再评价责任主体提出建议。 Finally, to our country already listed drug again evaluation responsibility subjects are proposed. 结果和结论：由于已上市药品再评價是一项系统性的工程，所以药品的生产、流通、使用、监督管理等环节所涉及的生产、经營企业、医疗机构、政府机关等都应担负起药品上市后再评价的工作。 Results and conclusion: because already listed drug again evaluation is a systematic project, so drug production, circulation, use, supervision and management involved production, trading enterprises and medical organizations, government agencies, etc. Are all should shoulder the drugs listed again after the evaluation work. 还可建立第三方评价機构参与完成已上市药品再评价工作。 Still can establish third-party evaluation institutions involved in complete already listed drug again evaluation.
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希望能帮助你The name of an unbranched acyclic mono-or di-aldehyde is formed by goal: This article through the Chinese and foreign law contrast research, the related legal framework research, the hospital management system research and so on to make in the drugs re-evaluation related laws and regulations to be related the main body and the responsibility proposes the basis. Method: Went on the market the drugs re-evaluation present situation take our country as the foundation, plans to choose the re-evaluation possible responsibility main body to carry on feasibility studies and so on capacity, right ability, responsibility ability. Carries on the analysis according to the existing laws and regulations to the drugs re-evaluation responsibility main body's localization, judges its feasibility, or needs to consummate content. Takes the reference by the overseas drugs re-evaluation system to the responsibility main body's localization, according to &Pharmaceuticals administration& the request, embarks from our country's actual situation, proposed that the proper responsibility main body, the classification induces various responsibilities main body the right and the duty. Finally, went on the market the drugs re-evaluation responsibility main body to our country to put forward the proposal. Result and conclusion: Because went on the market the drugs re-evaluation is a systematic project, therefore links and so on drugs production, circulation, use, management by supervision involve after the production, the Operation of business, the Medical establishment, the Governmental agency and so on should shoulder drugs going on the market, re-evaluation work. May also establish the third party appraisal organization to participation completes went on the market the drugs re-evaluation work.
Objective: this paper through comparative study and foreign law and relevant legal system research, hospital management system research, etc. For formulating drug regulations related to reassess its responsibilities related subject proposed basis. Methods: in our country has already listed drug again based evaluation actuality, plan to choose again evaluation may behave in the main responsibility of the ability, the rights of competence, responsibility ability feasibility study. According to the existing laws and regulations on drug evaluation responsibility subject localization again analysis, judge its feasibility, or need to consummate content. With foreign drugs again evaluation system for main responsibility orientation as reference, according to the requirements of the &drugadministration law, from the actual situation in our country, the paper points out the liability subject classification should be induces the main responsibility of rights and obligations. Finally, to our country already listed drug again evaluation responsibility subjects are proposed. Results and conclusion: because already listed drug again evaluation is a systematic project, so drug production, circulation, use, supervision and management involved production, trading enterprises and medical organizations, government agencies, etc. Are all should shoulder the drugs listed again after the evaluation work. Still can establish third-party evaluation institutions involved in complete already listed drug again evaluation. 双語对照查看
Objective: this paper through comparative study and foreign law and relevant legal system research, hospital management system research, etc. For formulating drug regulations related to reassess its responsibilities related subject proposed basis. Methods: in our country has already listed drug again based evaluation actuality, plan to choose again evaluation may behave in the main responsibility of the ability, the rights of competence, responsibility ability feasibility study. According to the existing laws and regulations on drug evaluation responsibility subject localization again analysis, judge its feasibility, or need to consummate content. With foreign drugs again evaluation system for main responsibility orientation as reference, according to the requirements of the &drugadministration law, from the actual situation in our country, the paper points out the liability subject classification should be induces the main responsibility of rights and obligations. Finally, to our country already listed drug again evaluation responsibility subjects are proposed. Results and conclusion: because already listed drug again evaluation is a systematic project, so drug production, circulation, use, supervision and management involved production, trading enterprises and medical organizations, government agencies, etc. Are all should shoulder the drugs listed again after the evaluation work. Still can establish third-party evaluation institutions involved in complete already listed drug again evaluation.
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