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

机译:来自CPHI全球2013年的报告,第五届年度预连接大会(2013年10月22日至24日 - 法兰克福,德国)

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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:2013年制药成分(CPHI)开始前一天全球,世界领先的药品网络活动,一些与会者聚集在一起为第五届年度核准会议,讨论业务发展,制造和监管竞技场的趋势。在会议上提供的六个模块中,人们致力于新兴市场的采购环境,特别关注印度和中国的发展。其他模块评估了新兴市场在新兴市场中创建仿制机和超级主义的趋势。此外,还有关于围绕的监管和发展障碍的问题的更新,即生物仿制和生物遗传士今天面临。两个讨论的共同主题包括用于泛型和生物仿制性的适当定价和侵蚀人口统计数据,许可情景,商业化战略以及如何保持竞争力,并在新的送货系统中找到新颖的创新,改进的配方和修改,以创造更好的优质活性药物成分。

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