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非临床
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  non-clinical
    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
    Non-clinical Laboratory Safety Studies of Pirfenidone
    吡非尼酮的非临床安全性评价
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    Viewpoint on Non-clinical Pharmacokinetic Evaluation of Traditional Chinese Medicine and Natural Medicine
    中药与天然药物非临床药代动力学评价的思考
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。
短句来源
    This paper analyzed and expressed the relationship and difference between non-clinical trial and ADR monitoring, lead a comprehensive understanding of drug safety evaluation.
    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。
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  “非临床”译为未确定词的双语例句
    Nonclinical safety evaluation of pediatric drug products in juvenile animals
    儿童用药物非临床安全性评价
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    Nonclinical safety evaluation of drug combinations(FDA)
    美国食品药品监督管理局复方制剂非临床安全性评价指导原则介绍
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    Safety evaluation for topical imiquimod cream in animals
    咪喹莫特乳膏的非临床安全性评价
短句来源
    In view of the diversity and complexity of drugs and many other factors involved, the authors suggest that the primary starting-point in the consideration of non-clinic test on the pharmacokinetics of quick-and slow-release dosages is to ensure the safety of patients and the effects of drugs and to elaborate the scheme of the test and assess it scientically and rationally in accordance with the characteristics of different kinds of drugs.
    由于药物的多样性和复杂性以及其所涉及的诸多因素,作者建议研制者在考虑进行速释、缓释等制剂的非临床药代动力学试验时,应主要考虑的出发点是基于保证临床病人的安全、有效,并针对不同药物的特点,科学、合理地进行试验设计和评价。
短句来源
    Finally the GLP to be carried out may improve medicine quality in non-security evaluation study,reduce man-made error,obtain experiment data of high reliability and ensure medicine security.
    实施GLP可以提高药品非临床安全性评价研究的质量 ,减少人为误差 ,得到可信性高的实验数据 ,以保障人民用药安全。
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  non-clinical
The instrument is especially suited for outcome assessment in various clinical and non-clinical populations and takes an average of about 30-45 min to complete.
      
A non-clinical cohort that had been assessed from 1978 to 1993 at 5 yearly intervals and that had a high prevalence rate of lifetime depression took part in the study.
      
A non-clinical cohort of 156 subjects was assessed on four occasions over 15 years, with 35% having had a major depression and 22% a minor depression at the most recent assessment.
      
The questionnaire was administered to psychiatric (n= 116), medical (n= 114) and non-clinical samples (n = 110).
      
In a sample of 30 non-clinical subjects the temporal stability of the FAD was investigated.
      
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In view of the diversity and complexity of drugs and many other factors involved, the authors suggest that the primary starting-point in the consideration of non-clinic test on the pharmacokinetics of quick-and slow-release dosages is to ensure the safety of patients and the effects of drugs and to elaborate the scheme of the test and assess it scientically and rationally in accordance with the characteristics of different kinds of drugs.

由于药物的多样性和复杂性以及其所涉及的诸多因素,作者建议研制者在考虑进行速释、缓释等制剂的非临床药代动力学试验时,应主要考虑的出发点是基于保证临床病人的安全、有效,并针对不同药物的特点,科学、合理地进行试验设计和评价。

GLP is a current international standard for non-clinic al laboratory study. During the implementation, based on qualified hardware, we sh ould strengthen organization system, set up awareness and stress quality managem ent.

GLP是国际通行的药品非临床试验质量管理规范 ,实施过程中 ,在整备合格的硬件设施前提下 ,应该加强GLP组织体制、GLP意识、重要环节的质量管理等软件建设

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。

 
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