本文選題：病例報告表 + 臨床試驗��； 參考：《藥學(xué)學(xué)報》2015年11期

【摘要】：病例報告表(CRF)是臨床試驗收集數(shù)據(jù)的主要文件,設(shè)計良好的CRF有助于數(shù)據(jù)庫的構(gòu)建,提高收集數(shù)據(jù)的準(zhǔn)確性,減少數(shù)據(jù)質(zhì)疑,方便研究者填寫且易于統(tǒng)計分析。CRF設(shè)計流程應(yīng)當(dāng)規(guī)范,數(shù)據(jù)采集須符合試驗方案要求。設(shè)計的CRF頁面應(yīng)布局清晰,字段設(shè)計及編碼應(yīng)規(guī)范。
[Abstract]:Case report form (CRF) is the main document of data collection in clinical trials. A well-designed CRF helps to build a database, improve the accuracy of data collection, and reduce data query. The design flow of CRF should be standardized and the data collection should meet the requirements of the test scheme. Designed CRF pages should be clearly laid out, and field design and coding should be standardized.
【作者單位】： 上海凱銳斯生物科技有限公司;
【分類號】：R969.4
，

本文編號：2040484