Challenges and prospects in Chinese pharmaceutical regulatory environment

Swagatika Tripathy, P. Murthy, BP Patra, P. Mehra, H. Dureja
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引用次数: 3

Abstract

Background China’s pharmaceutical market is growing at a healthy pace. This is due to potential rising per capita income, an increasing elderly population, urbanisation demographics and more access to health care. Methodology The methodology used is a comparative study on the basis of original empirical research. More specifically, the part of examination facts and regulation has been written by conducting empirical research on current international and national resource concerning the subject from books, various guidelines, rules and regulation, articles, published reports and internet. Results Generally the regulatory environment in China has been considered as an very challenging one. From regulatory perspective, CFDA regulations have not been stringent enough nor has it been robust enough to create a quality supply of medications, with (1) concerns in the subject matter, quality comparison between international regulatory standard and usually accepted local products and manufactures set standards; (2) a timeline for regulatory assessment and authorization of new drugs which is much longer in comparison to most countries; (3) less number of regulatory reviewer which has led to a backlog of earlier application. The journey to reshape China from ‘made-in-China’ to ‘discovered-in-China’ is highly challenging. (4) Complications with local protection, corruption and a lack of transparency. The directives from Government has recognized the need for significant system-level transformations for streamlining the pharmaceutical regulatory environment. Conclusion Continuing on the route of reform is promising that all Chinese citizens is eventually having access to safe, effective and high-quality medications in affordable price. These reformations are encouraging and promising not only for China’s health care system, but also for global Pharmaceutical industry and that’s the reason, now many big Pharma companies are considering China as a prime focus. The companies need to make use of the new opportunities, accessible to experience the benefit of faster time-to-market, and cause rewarding growth prospect for both domestic/ multinational companies.
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中国药品监管环境的挑战与展望
中国医药市场正以健康的速度增长。这是由于人均收入可能增加、老年人口增加、城市化人口结构以及获得医疗保健的机会增加。本文采用的研究方法是在原有实证研究的基础上进行的比较研究。更具体地说,考试事实和规则部分是通过对当前国际和国内有关该主题的资源进行实证研究而编写的,这些资源包括书籍、各种指南、规章制度、文章、发表的报告和互联网。结果总体而言,中国的监管环境被认为是一个非常具有挑战性的环境。从监管的角度来看,CFDA的监管不够严格,也不够健全,无法创造高质量的药品供应,存在以下问题:(1)对主题的关注,国际监管标准与通常接受的当地产品和制造商设定标准之间的质量比较;(2)与大多数国家相比,新药监管评估和授权的时间表要长得多;(3)监管审查人员较少,导致前期申请积压。重塑中国从“中国制造”到“中国发现”的过程极具挑战性。(4)地方保护、腐败和缺乏透明度等问题。政府的指示已认识到需要在系统一级进行重大改革,以简化药品管理环境。结论继续改革的道路是有希望的,所有中国公民最终都能以可承受的价格获得安全、有效、高质量的药物。这些改革不仅对中国的医疗保健系统,而且对全球制药行业都是令人鼓舞和充满希望的,这就是为什么现在许多大型制药公司都将中国视为主要焦点。公司需要利用新的机会,可以体验更快的上市时间的好处,并为国内/跨国公司带来有益的增长前景。
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