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How Civil Society Organisations Changed the Regulation of Clinical Trials in India

机译:民间社会组织如何改变印度临床试验的监管

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In 2005 India changed its pharmaceutical and innovation policy that facilitated a dramatic increase in international clinical trials involving study sites in India. This policy shift was surrounded by controversies; civil society organisations (CSOs) criticised the Indian government for promoting the commercialisation of pharmaceutical research and development. Health social movements in India fought for social justice through collective action, and engaged in normative reasoning of the benefits, burdens and equality of research. They lobbied to protect trial participants from structural violence that occurred especially in the first 5-6 years of the new policy. CSOs played a major role in the introduction of new regulations in 2013, which accelerated a decline in the number of global trials carried out in India. This activism applied interpretations of global social justice as key ideas in mobilisation, eventually helping to institutionalise stricter ethical regulation on a national level. Like government and industry, activists believed in randomised controlled trials and comparison as key methods for scientific knowledge production. However, they had significant concerns about the global hierarchies of commercial pharmaceutical research, and their impact on the rights of participants and on benefits for India overall. Pointing to ethical malpractices and lobbying for stricter ethical regulations, they aimed to ensure justice for research participants, and developed effective strategies to increase controls over the business side of clinical research.
机译:2005年,印度改变了其制药和创新政策,促进了涉及印度研究遗迹的国际临床试验的戏剧性增加。这种政策转变被争议包围;民间社会组织(CSOS)批评印度政府促进药品研发的商业化。印度的健康社会运动通过集体行动为社会正义而战,从事了对研究的福​​利,负担和平等的规范性推理。他们游说保护参与者免受结构暴力,特别是在新政策的前5-6岁处发生的结构暴力。 CSO在2013年引入新规定时发挥了重要作用,这加速了印度在印度进行的全球审判数量的下降。这种行动主义将全球社会正义的解释应用于动员中的关键思想,最终有助于制度化在国家一级更严格的道德规范。与政府和行业一样,活动家相信随机对照试验,并将其与科学知识生产的关键方法进行比较。然而,他们对商业药学研究的全球等级以及对参与者权利的影响以及整体对印度的福利的影响。指向道德弊端和游说进行更严格的道德规范,他们旨在确保研究参与者的正义,并制定了对临床研究业务方面的控制权的有效策略。

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