让跨部门的利益相关者参与医药质量研究工作:从STARmeds在印度尼西亚的研究中吸取教训
Amalia Hasnida1, Roland Bal2, Reise Manninda3
1Department of Health Care Governance, Erasmus School of Health Policy and Management, Erasmus University Rotterdam, Rotterdam, The Netherlands. hasnida@eshpm.eur.nl.
让多样化的利益相关者参与印尼药品质量研究是一项挑战,但至关重要. 合作建立了信任,改善了数据共享,并促进了更强大的研究和政策伙伴关系,以应对不合格的药物.
科学领域:
- 公共卫生 公共卫生
- 卫生政策 卫生政策
- 制药科学 制药科学
背景情况:
- 解决伪造和低标准药物的问题需要跨部门的合作和应用研究.
- 组织研究和让各种各样的利益相关者参与,以有效利用研究结果仍然是一个挑战.
研究的目的:
- 评估跨部门利益相关者参与印尼医学质量研究.
- 了解参与如何影响研究流程,参与者和结果的吸收.
主要方法:
- 使用绑架方法进行前性案例研究.
- 贡献映射和协作治理原则.
- 37次采访关键线人,24次会议观察和121次文件分析.
主要成果:
- 参与医药质量研究的利益相关者是可行的,但具有挑战性.
- 利益相关方,包括国家药物监管机构的更多参与,促进了共享的理解.
- 利益相关者参与提供了关键数据,影响了研究决策,并改善了研究结果的解释.
结论:
- 尽管面临挑战,跨部门利益相关者参与医学质量研究是有益的.
- 参与建立了信任,建立了网络,使监管机构接触到新的方法,并激发了新的角色.
- 该研究推进了关于制药主题的研究政策伙伴关系论坛.
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