在质量控制实验室中通过质谱测量实施多属性方法的合规性和监管考虑
Annick Gervais1, Eef H C Dirksen2, Thomas Pohl3
1Analytical Development Sciences for Biologicals, UCB, Chemin du Foriest, 1420 Braine L'Alleud, Belgium.
概括
本文为在质量控制实验室中使用片映射液体染色体质谱法实施多属性方法 (MAM) 提供了指导. 它重点关注生物制药批量释放和稳定性测试的良好制造实践 (GMP) 合规性和监管方面.
科学领域:
- 生物制药学分析分析
- 分析化学是一种分析化学.
- 质量控制 质量控制
背景情况:
- 使用质谱的多属性方法 (MAM) 对于生物制药的表征至关重要.
- 由于技术,合规性和监管方面的担忧,在批量释放和稳定性测试的质量控制 (QC) 中广泛采用良好制造实践 (GMP) 是有限的.
研究的目的:
- 为在质量控制实验室中实施MAM提供指导.
- 为了解决MAM采用的GMP合规性和监管考虑.
- 在第1部分中发表的先前的技术考量基础上建立.
主要方法:
- 基映射液体染色学-质谱学 (MAM) 是讨论的核心技术.
- 根据主要生物技术公司的行业专家共识,制定了指导方针.
- 专注于在GMP框架内的实际实施.
主要成果:
- 这篇文章详细介绍了对MAM实施至关重要的GMP合规性和监管方面.
- 它解决了挑战,并提供了将MAM集成到QC工作流程中的解决方案.
- 专家的见解有助于生物制药质量控制实验室更顺利地过渡.
结论:
- 在质量控制中成功实施MAM需要仔细考虑GMP和监管环境.
- 本指南旨在增加行业对MAM的信心和接受,以便用于例行测试.
- 行业专家之间的合作确保了全面和实际的建议.
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