双重用途研究和在高收入国家使用增强病原体的研究:是谁的生意?
Nir Eyal1, Melkizedeck Leshabari2, Malabika Sarker3,4
1Center for Population-Level Bioethics (IFH), HBSP (SPH), and Philosophy (SAS), Rutgers University, New Brunswick, New Jersey, USA.
mSphere
|June 13, 2024
概括
美国对双重用途研究的新规定可能会引起关注,并增强流行病原体. 该研究认为,塑造这些关键政策需要来自不同科学和国际视角的投入,而不仅仅是美国的病毒学家.
科学领域:
- 生物安全和生物安全.
- 传染病研究 传染病研究
- 公共卫生政策 公共卫生政策
背景情况:
- 美国有关双重用途的研究 (DURC) 和具有大流行潜力的增强病原体 (ePPP) 的研究的规定可能会发生变化.
- 广泛的讨论集中在这种研究的最佳监管框架上.
- 然而,程序性方面 - - 具体来说,谁应该参与制定这些法规 - - 仍未得到充分探讨.
研究的目的:
- 解决适当的利益相关者参与美国DURC和ePPP法规制定的程序问题.
- 提出一个关于生物安全和生物安全研究政策的包容性审议和决策流程的框架.
主要方法:
- 本评论分析了监管发展的程序性方面.
- 它倡导采取广泛和包容性的政策制定方法.
- 该分析基于科学治理和公众审议的原则.
主要成果:
- 评论认为,目前的监管讨论可能过于狭地集中在一小群专家身上.
- 它强调需要纳入更广泛的视角,以确保稳健有效的监管.
- 调查结果表明,一个更具包容性的过程将更好地服务于科学界和公共安全的利益.
结论:
- 建议美国病毒学家和更广泛的科学界将受益于在监管塑造中包括多元化的声音.
- 涉及外部专家和国际利益相关者对于制定全面和全球相关政策至关重要.
- 制定法规的包容性方法对于对具有重大影响的生物研究进行负责任的监督至关重要.
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