基于ICH Q14原则的分析程序开发和生命周期管理的现代框架
Max Eberle1, Jamie T Wasylenko2, Drazen Kostelac1
1AbbVie Deutschland GmbH & Co. KG, 67061 Ludwigshafen am Rhein, Germany.
Analytical chemistry
|December 20, 2024
概括
本研究提出了一项采用新制药分析方法指南 (ICH Q14/Q2(R2),USP 1220) 的策略. 该方法使用设计时分析质量 (AQbD) 来简化分析方法的开发和生命周期管理.
科学领域:
- 制药科学 制药科学
- 分析化学 分析化学
- 监管科学 监管科学
背景情况:
- 目前的分析方法验证依赖于ICH Q2 (R1) (2005) 准则.
- 药品提交越来越多地采用整体的,基于风险的控制策略.
研究的目的:
- 提出实施最新分析方法指南 (ICH Q14/Q2(R2),USP 1220) 的战略.
- 将ICH Q14的关键元素集成到一个分析质量设计 (AQbD) 框架中.
主要方法:
- 探索当前的验证实践.
- 讨论ICH Q14元素:分析目标配置文件 (ATP),知识管理,风险评估,绩效监测.
- 将其整合到开发和生命周期管理的AQbD框架中.
主要成果:
- 拟议的战略与生命周期方法和基于风险的控制策略保持一致.
- 实施需要平衡批准后的灵活性效益与资源投资.
- 该战略旨在简化分析开发和简化方法生命周期管理.
结论:
- 采用ICH Q14/Q2 ((R2) 和USP 1220需要一个生命周期和AQbD方法.
- 基于风险的策略增强了方法的理解,并简化了管理.
- 这种转变有望在制药行业带来更高效,更强大的分析程序.
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