摘要
目的:促进临床试验药物管理中记录表的规范应用。方法:按照我院临床试验药物的管理流程阐述各环节记录表的设计和应用体会。结果与结论:一套设计规范的记录表能有效减少信息遗漏,能够提高临床试验药物管理中包括储藏、温/湿度、接收、发放/回收、退还等环节的记录质量。
OBJECTIVE： To promote standard application of record list in drug management of clinical trial. METHODS： The design and experience of record list were introduced according to management process of drugs for clinical trials in our hospital. RESULTS ＆ CONCLUSIONS： A set of standard record list is beneficial to reducing loss of data, and improving the quality of records about storage, temperature, reception, dispensing, recycle and rejection in drugs management of clinical trial.
出处
《中国药房》
CAS
CSCD
北大核心
2011年第17期1572-1573,共2页
China Pharmacy
关键词
药物
临床试验
记录表
Drug
Clinical trial
Record list
