一个质量管理系统,旨在确保格洛科马注册处的监管级数据质量
Shinsuke Wada1, Satoru Tsuda2, Maiko Abe2
1Division of Drug Development and Regulatory Science, Graduate School of Pharmaceutical Sciences, Keio University, Tokyo, Japan.
PloS one
|June 2, 2023
概括
一个质量管理系统被开发为日本眼患者登记,以确保监管级数据的长期结果评估. 该系统增强了患者登记册对药物评估和临床实践见解的实用性.
科学领域:
- 眼科医生 眼科 眼科
- 临床研究 临床研究
- 数据管理数据管理
背景情况:
- 患者注册表在临床试验中为药物评估提供了优势,包括长期数据修复和现实世界结果洞察力.
- 确保注册表中的数据质量对于监管决策和可靠的临床评估至关重要.
- 本研究的重点是日本青光眼患者登记,以确保长期结果评估的监管级数据质量.
研究的目的:
- 为日本一家绿眼病患者登记处建立质量管理系统.
- 确保生成监管级数据,以评估患者的长期治疗结果.
- 加强在药物的临床评估中利用患者登记册.
主要方法:
- 使用基于风险的方法建立了质量管理系统,参考ICH-E6 (R2) 建议.
- 关键组成部分包括建立治理,计算机化系统验证 (CSV) 和风险评估/控制.
- 制定和实施了标准操作程序,数据管理计划和风险控制计划.
主要成果:
- 通过学术合作建立了治理结构,并制定了15个标准操作程序.
- 电子数据捕获 (EDC) 系统得到了验证,并确定了质量关键因素.
- 实施了风险控制计划,解决了大多数监管质量建议,尽管两个没有得到满足.
结论:
- 一个质量管理系统成功地建立和配置了青光眼注册表.
- 该系统确保适合目的的数据质量,用于监管目的和未来的长期后续行动.
- 这有助于可靠地治愈长期患者的结局数据在玻璃眼.
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