The global biopharma industry and the rise of Indian drug multinationals: implications for Australian generics policy.

Hans Löfgren
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引用次数: 17

Abstract

This article provides a synopsis of the new dynamics of the global biopharma industry. The emergence of global generics companies with capabilities approximating those of 'big pharma' has accelerated the blurring of boundaries between the innovator and generics sectors. Biotechnology-based products form a large and growing segment of prescription drug markets and regulatory pathways for biogenerics are imminent. Indian biopharma multinationals with large-scale efficient manufacturing plants and growing R&D capabilities are now major suppliers of Active Pharmaceutical Ingredients (APIs) and generic drugs across both developed and developing countries. In response to generic competition, innovator companies employ a range of life cycle management techniques, including the launch of 'authorised generics'. The generics segment in Australia will see high growth rates in coming years but the prospect for local manufacturing is bleak. The availability of cheap generics in international markets has put pressure on Pharmaceutical Benefits Scheme (PBS) pricing arrangements, and a new policy direction was announced in November 2006. Lower generics prices will have a negative impact on some incumbent suppliers but industrial renewal policies for the medicines industry in Australia are better focused on higher value R&D activities and niche manufacturing of sophisticated products.

全球生物制药工业和印度跨国制药公司的崛起:对澳大利亚仿制药政策的影响。
本文概述了全球生物制药行业的新动态。能力接近“大型制药公司”的全球仿制药公司的出现加速了创新者和仿制药部门之间界限的模糊。基于生物技术的产品在处方药市场中占据了一个巨大且不断增长的部分,生物仿制药的监管途径迫在眉睫。印度生物制药跨国公司拥有大规模高效的制造工厂和不断增长的研发能力,现在是发达国家和发展中国家活性药物成分(api)和仿制药的主要供应商。为了应对仿制药竞争,创新公司采用了一系列生命周期管理技术,包括推出“授权仿制药”。未来几年,澳大利亚的仿制药市场将出现高增长,但当地制造业的前景黯淡。国际市场上廉价仿制药的供应给药品福利计划(PBS)的定价安排带来压力,2006年11月宣布了一项新的政策方向。较低的仿制药价格将对一些现有供应商产生负面影响,但澳大利亚医药行业的产业更新政策更侧重于高价值的研发活动和尖端产品的利基制造。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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