桥梁指导和法规:解释关于GMP制造业的人工智能的附件22草案
Mario Stassen1, Matt Schmucki2, Fransisco Barranco3
1Department of Life Sciences Innovation, Stassen Pharmaconsult BV, Aerdenhout, The Netherlands.
PDA journal of pharmaceutical science and technology
|February 16, 2026
概括
本文解释了欧洲药物局关于用于制药制造的人工智能 (AI) 的附件22草案. 它将人工智能采用与持续流程验证 (CPV) 监管合规性建议保持一致.
科学领域:
- 制药制造业 制药制造业 制药制造业
- 监管科学 监管科学
- 人工智能的人工智能
背景情况:
- 制药行业越来越多地采用人工智能 (AI).
- 持续过程验证 (CPV) 为人工智能应用提供了一个框架.
- 欧洲药品管理局 (EMA) 发布了关于AI在制药生产中的附录22草案.
研究的目的:
- 解释EMA关于AI在GMP监管的制药制造业中的附录22草案.
- 检查附件22与CPV建议之间的一致性.
- 为符合AI实施提出路线图.
主要方法:
- 文献审查和对EMA草案附件22的解释.
- 对附件22与CPV建议之间的调整分析 (Stassen等人,2025).
- 开发概念框架和工作流图案.
主要成果:
- 确定了附件22与CPV原则之间的趋同.
- 突出了人工智能实施中的运营挑战.
- 提出了一份协调人工智能治理和合规性的路线图.
结论:
- 欧洲药物管理协会 (EMA) 草案附件22提供了基于风险的AI在制药生产中的框架.
- 协调CPV原则与附件22期望对于合规至关重要.
- 积极的AI治理对于制药行业的准备工作至关重要.
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