發(fā)布時(shí)間：2018-06-19 16:27

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

【摘要】：病例報(bào)告表(CRF)是臨床試驗(yàn)收集數(shù)據(jù)的主要文件,設(shè)計(jì)良好的CRF有助于數(shù)據(jù)庫(kù)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(jì)分析。CRF設(shè)計(jì)流程應(yīng)當(dāng)規(guī)范,數(shù)據(jù)采集須符合試驗(yàn)方案要求。設(shè)計(jì)的CRF頁(yè)面應(yīng)布局清晰,字段設(shè)計(jì)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(hào)】：R969.4
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本文編號(hào)：2040484