泰亨实业 Information

自2005年起，泰亨始终为全球仿制药企业提供药物垂直整合开发项目服务。从原料药研发到制剂产品市场推广，我们为客户提供全方位的药物开发解决方案。我们的服务涵盖药物开发的整个生命周期，从实验阶段的研发，工艺优化和放大，分析，到其它质量控制方法，批量生产，GMP管理，药政支持以及申报批准后的产品生命周期管理。 泰亨实业位于中国上海，自2009年以来，多次经历美国FDA的检查。凭着执着精神和坚定的质量承诺，我们达到了 最严格的药物开发标准。 我们的项目和质量管理团队拥有丰富的知识和实践经验，能够了解和满足客户的需求。为客户寻找从开发到商业化的最合理， 且最具成本效益的途径是我们团队的终极目标。 Since 2005, Tai Heng has been servicing global generic companies through vertically integrated drug development program. From API to commercial product, we offer customers a complete and integrated solution for pharmaceutical development. Our services cover entire spectrum of drug development life cycle, from benchtop development, scale up, process optimization, analytical and other quality control methods, submission batch manufacturing, GMP management, regulatory support, and post approval product life cycle management. Located in Shanghai, China, our facility has been inspected by US FDA multiple times since 2009. With dedication and steadfast quality commitment, we are able to meet the most stringent drug development standards. Our project and quality management team, each with extensive knowledge and hands-on experience, understand and appreciate our customer’s needs. Finding the most rational and cost-effective route from development to commercialization for our customer is the ultimate achievement for our project team.