The global economic crisis and its impact on public finances in most developed countries are giving rise to cost-containment policies in health'/> The pharmaceutical industry and the sustainability of healthcare systems in developed countries and in Latin America
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The pharmaceutical industry and the sustainability of healthcare systems in developed countries and in Latin America

机译:发达国家和拉丁美洲的制药业和医疗体系的可持续性

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> face="Verdana, Arial, Helvetica, sans-serif" size="2">The global economic crisis and its impact on public finances in most developed countries are giving rise to cost-containment policies in healthcare systems. Prevailing legislation on medication requires the safety, quality, and efficacy of these products. A few countries include efficiency criteria, primarily for new medication that they wish to include in public financing. The appropriate use of generic and "biosimilar medication" is very important for maintaining the financial equilibrium of the Health Services. The problem in Latin America is that not all multisource products are bioequivalent and not all countries have the resources to conduct bioequivalence studies in vivo. The European Medicines Agency in 2005 adopted guidelines on "biosimilar medicines" and thirteen of them were subsequently approved for general release. Benchmarking of this model by other countries would be important. The influence of the pharmaceutical industry on political and administrative areas is enormous and control is necessary. The pharmaceutical companies claim that they act with corporate social responsibility, therefore, they must ensure this responsibility toward society.
机译:> face =“ Verdana,Arial,Helvetica,sans-serif” size =“ 2”>在大多数发达国家,全球经济危机及其对公共财政的影响正在引起医疗保健系统的成本控制政策。现行的药物法规要求这些产品的安全性,质量和功效。一些国家/地区包含了效率标准,主要针对希望纳入公共资金的新药物。适当使用仿制药和“生物仿制药”对于维持卫生服务的财务平衡非常重要。拉丁美洲的问题在于,并非所有的多来源产品都是生物等效的,而且并非所有国家都有资源进行体内生物等效性研究。欧洲药品管理局(European Medicines Agency)在2005年通过了有关“生物仿制药”的指南,随后批准了其中的13种药物进行一般发布。其他国家对该模型进行基准测试将很重要。制药业对政治和行政领域的影响是巨大的,必须加以控制。制药公司声称他们具有企业社会责任,因此,他们必须确保对社会承担这种责任。

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