从临床试验到商业化:人类疫苗的前景
Nidhi Mehrotra1, Padmavati Manchikanti2
1Rajiv Gandhi School of Intellectual Property Law, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, 721302, India.
Pharmaceutical research
|December 10, 2025
概括
印度 印度 印度
科学领域:
- 制药科学 制药科学
- 监管事务 监管事务
- 临床试验管理 临床试验管理
背景情况:
- 印度是全球主要的疫苗生产国和出口国.
- 然而,与G20国家相比,印度在推出新疗法方面经历了显著的延迟.
研究的目的:
- 评估利益相关者对2019年新药和临床试验 (NDCT) 规则的看法.
- 评估这些规则对制药公司的连贯性,清晰性和运营影响.
主要方法:
- 对利益相关者的反进行定性分析.
- 根据2019年NDCT规则,确定制药公司面临的关键挑战.
主要成果:
- 确定了三个主要挑战集群:监管,运营和系统.
- 监管问题包括漫长的审批时间和不清楚的法律框架.
- 运营和系统障碍涉及试验场地分配,容量,伦理委员会延误和不一致的指导方针.
结论:
- 2019年NDCT规则为印度的制药公司带来了重大监管,运营和系统性挑战.
- 解决这些障碍对于加速治疗推出和改善印度药物开发环境至关重要.
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