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非临床研究
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  non-clinical study
     A Preliminary Discussion on Non-Clinical Study and ADR Monitoring
     浅谈非临床研究与ADR监测
短句来源
  “非临床研究”译为未确定词的双语例句
     Hubei center for safety evaluation of drugs passed the inspection of authentication of GLP, which organized by the National Food and Drug Supervision Administration in December, 2004 and became the first authenticated GLP research institute of the province.
     湖北省药物安全性评价中心于2004年12月一次性通过了国家食品药品监督管理局组织的“药物非临床研究质量管理规范”(GLP)认证检查,成为GLP研究机构,为湖北省首家通过GLP认证的单位。
短句来源
     The Good Laboratory Practices for non-clinical laboratory studies (the GLP regulations) is a quality system concerned with the organizational process and the conditions under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, archived and reported.
     非临床研究质量管理规范(GLP)是一种与非临床健康和环境安全性研究的计划、实施、监督、记录、报告和建档有关的,涉及组织过程与条件的质量体系。
短句来源
     Obsessive-compulsive symptoms are highly-occurred mental problems among undergraduates. At present, most researches of obsessive-compulsive symptoms are mainly focused on the clinical community.
     强迫症状是大学心理问题中发生率较高的一种,现有研究大多集中在临床领域,专门针对大学生强迫症状的非临床研究并不多见。
短句来源
     The safety evaluation of drugs refers to drugs non-clinical safety evaluation, or drugs non-clinical research, whose quality management practices are called Good Laboratory Practice (GLP).
     药物安全性评价是指药物非临床安全评价即药物非临床研究,药物非临床研究质量管理规范即GLP。
短句来源
     The former stage includes non-clinical trial and clinical trial study while the latter is ADR monitoring stage.
     药品上市前的安全性评价即非临床研究各项毒性实验以及新药临床试验 (Ⅰ ,Ⅱ ,Ⅲ期 ) ,而上市后的安全性评价则属于ADR监测范畴。
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  相似匹配句对
     Design Nonrandomized clinical trial.
     设计随机化临床试验。
短句来源
     AN ANALYSIS OF CLINICAL INFECTION OF NON-FERMENTING BACTERIA
     发酵菌临床感染分析
短句来源
     Clinical Application of Aspheric Intraocular Lenses
     球面人工晶状体的临床应用研究
短句来源
     Sorafenib: pharmacology and clinical studies
     索拉尼的药理及临床研究
短句来源
     A Clinical Study of Unrelated Hematopoietic Stem Cell Transplantation
     血缘造血干细胞移植的临床研究
短句来源
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  non-clinical study
A second non-clinical study showed that androgens seem to have no effect.
      


To be safety is the elementary requirement for drugs. The evaluation of drug safety should be made from both pre-marketing stage and post-marketing stage. The former stage includes non-clinical trial and clinical trial study while the latter is ADR monitoring stage. This paper analyzed and expressed the relationship and difference between non-clinical trial and ADR monitoring, lead a comprehensive understanding of drug safety evaluation.

“安全性”是药品基本要求之一 ,对药品安全性的评价则应从药品上市前、后两个阶段进行。药品上市前的安全性评价即非临床研究各项毒性实验以及新药临床试验 (Ⅰ ,Ⅱ ,Ⅲ期 ) ,而上市后的安全性评价则属于ADR监测范畴。本文旨在通过对药品非临床研究与ADR监测区别与联系的分析 ,阐明二者之间的联系 ,使人们对药品安全性评价加以全面的认识。

Safety pharmacology is an integrated discipline that has evolved from the distinct fields of pharmacology, physiology and toxicology. Safety pharmacology studies identify, monitor and characterize potentially undesirable pharmacodynamic activities in non-or pre-clinical studies. In this paper the actuality of safety pharmacology is analyzed, the basic request of experiment design is discussed, and the standardization of design for the experiment of central nervous system, cardiovascullar system and respiratory...

Safety pharmacology is an integrated discipline that has evolved from the distinct fields of pharmacology, physiology and toxicology. Safety pharmacology studies identify, monitor and characterize potentially undesirable pharmacodynamic activities in non-or pre-clinical studies. In this paper the actuality of safety pharmacology is analyzed, the basic request of experiment design is discussed, and the standardization of design for the experiment of central nervous system, cardiovascullar system and respiratory system is discussed.

安全药理学是从药理学、生理学和毒理学发展而来的一门独立的综合性药理学学科。安全药理学研究之目的是识别、监控并确定非临床研究中出现潜在的不期望的药效活性。本文分析安全药理学的现状,讨论实验设计的基本要求,对中枢神经系统、心血管系统和呼吸系统实验设计的规范化提出了建议。

The aim of this paper is arousing the people to understand the importance and the purpose of the drugs reevaluation.Combining the present condition of domestic and international drugs reevaluation,it sets forth the necessity and urgency of drug reevaluation on the reference value of both the no-clinical study and the limited clinics study.

本文以保障人民用药安全有效为出发点,旨在唤起人们对药品再评价重要性的认识以及再评价所要达到的目的。结合国内、外药品再评价的现状,从非临床研究的参考价值和临床研究的局限性阐述了药品再评价的必要性与紧迫性。

 
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