世卫组织对类似生物治疗胰岛素的预资格的障碍
1Innovation and Emerging Technologies Department, Access to Medicines and Health Products Division, World Health Organization, 20 Avenue Appia, 1211Geneva, Switzerland.
Bulletin of the World Health Organization
|October 28, 2024
概括
类似生物治疗性人体胰岛素的制造商面临世界卫生组织 (WHO) 预资格的障碍,包括缺乏投资回报保证和复杂的要求. 解决这些问题对于更广泛地参与世卫组织计划至关重要.
科学领域:
- 制药科学 制药科学
- 生物技术是生物技术.
- 公共卫生 公共卫生
背景情况:
- 世界卫生组织 (WHO) 的预资格计划对于确保生物治疗产品 (包括人体胰岛素) 的质量至关重要.
- 类似的生物治疗人类胰岛素产品在全球糖尿病管理中发挥着至关重要的作用.
研究的目的:
- 识别和分析阻碍类似生物治疗人类胰岛素制造商寻求世卫组织预资格的障碍.
- 了解公司在满足世卫组织对胰岛素产品的预资格要求时所面临的挑战.
主要方法:
- 一份自我管理的问卷被分发给20家类似生物治疗人类胰岛素的制造商.
- 收集的数据集中在产品细节,对世卫组织要求的了解,出口状态和良好制造实践 (GMP) 合规性.
- 答案被评估并进行主题分析.
主要成果:
- 获得了55%的响应率,揭示了五个主要主题:制造商/产品,意识/参与,技术援助需求,市场/供应链问题和良好生产规范批准.
- 世卫组织预资格参与的主要障碍包括缺乏投资回报机制的保证,以及对生物类似胰岛素的要求的复杂性.
结论:
- 加强参与世卫组织预资格计划需要国际采购机构建立预购协议.
- 世卫组织的当地生产和援助部门应为胰岛素制造商提供持续的技术支持,以帮助他们开发产品并遵守良好的生产规范.
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