关于制药制造业设计质量工具的最新选
Evren Algın Yapar1, Merve Nur Özdemir1,2
1Department of Pharmaceutical Technology, Faculty of Pharmacy, Sivas Cumhuriyet University, Sivas, Türkiye.
Combinatorial chemistry & high throughput screening
|July 23, 2025
概括
设计质量 (QbD) 通过早期整合质量,降低成本和加快市场上市时间来增强制药开发. 这种系统的,数据驱动的方法通过风险和知识管理来确保一致的产品质量.
科学领域:
- 制药科学 制药科学
- 药物开发 药物开发
- 质量保证 质量保证 质量保证
背景情况:
- 传统的制药开发是耗时的,昂贵的,具有挑战性的.
- 设计质量 (QbD) 是一种监管认可的方法,专注于从设计阶段开始将质量构建到产品中.
- QbD集成了质量风险管理和知识管理,以实现高效的制药开发.
研究的目的:
- 审查设计质量 (QbD) 对制药产品的影响.
- 检查QbD内部质量风险管理和知识管理的作用.
- 探索QbD在新药和仿制药制造中的应用.
主要方法:
- 从PubMed,ScienceDirect和Google Scholar等数据库中对同行评审文章 (2009-2025) 进行全面的文献搜索.
- 使用EPO,USPTO和谷歌专利数据库进行专利搜索.
- 分析QbD,QbD应用的剂量形式,质量风险管理和过程分析技术.
主要成果:
- 实施 QbD 会提高产品质量,降低成本,缩短上市时间.
- 质量风险管理和知识管理对于QbD成功至关重要.
- QbD适用于新药和仿制药的制造工艺.
结论:
- 设计质量为制药开发提供了一个科学,数据驱动和基于风险的战略.
- 包括风险和知识管理在内的QbD原则对于持续的药品质量至关重要.
- 该审查强调了QbD在制药行业的重大影响和未来前景.
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