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A report from CPhI worldwide 2013, Fifth Annual Pre-Connect Conference (October 22-24, 2013 - Frankfurt, Germany)

机译:CPhI 2013年全球报告,第五届年度连接前会议(2013年10月22日至24日,德国法兰克福)

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摘要

A day before the start of the 2013 Conference on Pharmaceutical Ingredients (CPhI) Worldwide, the world's leading pharmaceutical networking event, a number of attendees gathered for the Fifth Annual Pre-Connect Conference to discuss trends in business development, manufacturing and regulatory arenas. Of the six modules presented at the meeting, one was dedicated to the sourcing environment in emerging markets, with special attention paid to developments in India and China. Other modules evaluated the current trends in the creation of generics and supergenerics in emerging markets. Additionally, there were updates on issues surrounding the regulatory and development hurdles that biosimilars and biobetters are facing today. Common themes for both discussions include appropriate pricing and erosion demographics for generics and biosimilars, licensing scenarios, commercialization strategies, and how to stay competitive and find novel innovations within new delivery systems, improved formulations and modifications to create better quality active pharmaceutical ingredients.
机译:在全球领先的医药网络盛会2013全球医药成分会议(CPhI)召开的前一天,许多与会者聚集在第五届年度预连接会议上,讨论了业务发展,制造和监管领域的趋势。在会议上介绍的六个模块中,一个模块专门针对新兴市场的采购环境,并特别关注印度和中国的发展。其他模块评估了新兴市场中仿制药和超仿制药的当前趋势。此外,有关生物仿制药和生物仿制药今天面临的监管和发展障碍的问题也有最新动态。两次讨论的共同主题包括:仿制药和生物仿制药的适当定价和侵蚀人口统计数据,许可方案,商业化策略,以及如何在新的输送系统中保持竞争力并找到新颖的创新,改进的制剂和改进方法以生产质量更好的活性药物成分。

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