超越国界的信任:欧洲对药品获取的外部监管影响
Pramiti Parwani1,2,3, Katrina Perehudoff1,2,3, Anniek de Ruijter1,2
1https://ror.org/04dkp9463University of Amsterdam, Amsterdam Law School, Law for Health and Life, Netherlands.
概括
欧洲机构,如欧洲药品管理局 (EMA) 和欧洲专利局 (EPO),通过援助和合作,与低收入和中等收入国家 (LMICs) 建立"技术信任",扩大其监管影响力.
科学领域:
- 全球卫生治理全球卫生治理
- 制药法规 制药法规 制药法规
- 国际关系 国际关系
背景情况:
- 欧洲机构在全球范围内发挥着重要的监管影响.
- 了解这种外部监管影响的机制对于全球健康至关重要.
研究的目的:
- 调查欧洲外部监管对低收入和中等收入国家 (LMICs) 制药治理的影响背后的制度动态.
- 分析欧洲药品管理局 (EMA) 和欧洲专利局 (EPO) 在这一过程中的作用.
主要方法:
- 机构动态的定性分析.
- 专注于技术人员外展和欧洲监管机构与LMIC监管机构之间的合作.
主要成果:
- "技术专家的信任"是一个关键的动态,其特点是单方面关系,其中LMIC监管机构信任欧洲机构.
- 影响力通过技术援助,协作和分工来扩大.
- 国际框架加强了EMA和EPO的可信度.
结论:
- 欧洲的监管权力通过建立信任机制来扩大,这可能会影响小规模中小企业的监管自主权.
- 这项研究强调了全球卫生治理中对制药市场和LMICs在全球卫生治理中的准入的影响.
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