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临床试验数据管理之数据记录的常见问题

2012-12-13 MedSci MedSci原创

做临床试验的数据管理,那肯定需要对数据记录进行核查的,虽然有程序核查来完成大部分数据库核查工作,不过毕竟机器不是万能,还是有一些东西需要经验老道的数据管理员来完成的。所以特此将数据记录检查时的常见问题进行了归纳汇总: 1、违规与不规范 2、造假与不严谨 3、未做与不完整 4、组织与个人行为造假 可以详细分为以下几类: GCP规范操作核查存在主要数据问题 1.无原始病历或原始病历中无记录(缺

做临床试验的数据管理,那肯定需要对数据记录进行核查的,虽然有程序核查来完成大部分数据库核查工作,不过毕竟机器不是万能,还是有一些东西需要经验老道的数据管理员来完成的。所以特此将数据记录检查时的常见问题进行了归纳汇总: 1、违规与不规范 2、造假与不严谨 3、未做与不完整 4、组织与个人行为造假 可以详细分为以下几类: GCP规范操作核查存在主要数据问题 1.无原始病历或原始病历中无记录(缺或不全)        2.检验结果不能溯源(检验数据、心电图、X光片…)        3.无统计计划书和统计报告或数据管理无序        4.知情同意书缺失或签署存在问题 知情同意书检查时的常见问题 1.知情同意书丢失或不完整,且无合理解释        2.未签署知情同意书就进行研究,或先纳入、后签署     &n

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    2023-07-17 ms3000001527664206 来自吉林省
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临床试验数据管理之数据记录

一.数据记录的作用     记录是安全性、有效性的评价和报告依据,也是遵循GCP的证据, 只有存在记录: 1.才能证明相关行为发生过;        2.才能在发生任何问题时追根溯源;        3.才能证明试验是严格按照GCP、

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