《药物安全性评价》是2006年化学工业出版社出版的图书，作者是谢恩 C.加德。
GLP实验室软件建设及发展趋势 - 中国新药杂志 关键词： GLP；药物安全性评价；软件建设 [gap=706]Key words： good laboratory practice; drug safety evaluation; software construction
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临床前药物安全性评价 drug safety evaluation ; DSE
康龙化成今天宣布任命汪巨峰博士为公司高级副总裁并担任其药物安全性评价机构负责人。
Pharmaron today announced the appointment of Dr. Jufeng Wang, as Senior Vice President and Test Facility Manager (TFM) of its safety assessment facility in Beijing.
目的分析药物不良反应(adr)发生规律及特点，为临床合理用药及药物安全性评价提供依据。
Objectives Supply the evidence to clinic drug administrate and estimation of medicine safety dy analyzing the rule and characters of medicine adverse reaction.
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。
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).
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