投资4.5亿元建设原料药大平台，现拥有大小生产设备200余台套；上千万元的检测设备，红外、液质、ICP-MS、液相、气相一应俱全；现有员工400余名，技术人员从事研发、生产十余年，经验丰富；地处省级化工园区，建有污水处理设施，日处理能力150余方。现向社会招商，MAH委托加工、CMO代工、OEM加工任你选，欢迎各界朋友洽谈。

山东诚汇双达药业有限公司成立于2014年，位于德州市平原县经济开发区，总投资4.5亿元，占地178亩，总建筑面积8.26万平方米。公司注册资本1.1亿元，由山东诚创医药技术开发有限公司所属济南诚汇双达化工有限公司投资兴建，是山东诚创医药技术开发有限公司实施科技成果转化、产业化的重要基地。 Shandong Chenghui Shuangda Pharmaceutical Co., Ltd. was founded in 2014, which is located in economic development zone of Pingyuan County in Dezhou. The total investment is 450 million yuan and the registered capital is 110 million yuan, which is invested by Jinan Chenghui Shuangda   Chemical Co., Ltd. subordinated by Shandong Chengchuang Pharmaceutical R&D Co., Ltd.. It covers an area of 178 acres and the total construction area is 826,00 square meters. It is the important base of Shandong Chengchuang Pharmaceutical R&D Co., Ltd. for the transformation and industrialization of scientific and technological achievements. 山东诚汇双达药业有限公司是以原料药为主、制剂、食品、饲料添加剂为辅，满足国际认证及注册标准的高端综合产业基地。主要品种有局麻类用药、心脑血管系统用药、营养类用药、激素类用药、食品添加剂类五大系列，部分品种位居全球2-3位主供应商。公司具有世界先进水平的一流生产线，满足GMP、FDA等相关认证要求，建设有符合GMP生产的六个车间八条生产线，配备符合CGMP要求的研发转化实验平台、质量分析控制中心。 Shandong Chenghui Shuangda Pharmaceutical Co., Ltd. is a high-end comprehensive industrial base that meets international certification and registration standards, which produces APIs mainly and the auxiliary products are preparation, food and feed additives. The main varieties of the company are series of local anesthesia, cardiocerebral vascular, nutrition, hormone and food additive, some of which are the major suppliers in the world. The company has the world advanced level production line that meets the requirements of GMP, FDA and so on. There are eight production lines in six workshops satisfying GMP. The R&D transformation experiment platform and quality analysis and control center meet the requirement of CGMP. 生产能力Production capacity 公司现已完成两个车间4条GMP生产线建设，正在建设三、四、五三个车间3条GMP生产线，从而满足多功能、多产品的生产要求。 目前拥有反应设备200余套，拥有孕激素等特殊生产车间，能够处理氢化、高压及低温(-60℃）反应，可承接各种不同反应需求的品种生产。 The company has constructed four GMP production lines in two workshop and is building three GMP production lines in three workshop so that it can meet the multifunctional and multi-product  production demands. So far, there are more than 200 sets of reaction equipment and special production workshops with progesterone, which are able to handle hydrogenation, high pressure and low temperature (-60 ℃) reaction and can undertake various kinds of production with different demand. 环保能力Environmental protection ability 公司地处省级化工园区，环保、安全资质齐全，依托园区和自身能力，污水处理能力COD450万/天，保障了产品的绿色生产。 The company is situated in the provincial chemical industrial park, and has complete environmental protection and safety qualification. Relying on the park and its own capacity, the sewage treatment capacity is COD450 million per day, ensuring the green production. 质量控制Quality Control 公司拥有符合国内外要求质量控制体系，配备有液质联用、红外、液相及气相等共计300余种近1000万元分析质控仪器，并拥有一支10多年经验的质量控制团队，为产品的申报及未来的质量控制保驾护航。 The company has quality control system in accordance with domestic and international requirements and is equipped with  more than 300 kinds of quality control equipment of liquid chromatography-mass spectroscopy, infrared, liquid phase and gas phase. It has a quality control team with more than 10 years’ experience, which can guarantee the product declaration and quality control. 研发能力R & D capability 公司拥有一只拥有多名博士、硕士组成的研发团队，配备化学合成、生化技术等各方面人才，可完成路线开发、工艺对接及成果转化等工作，满足不同的合作需求。 The company has a R&D team with doctor and master's degree. It is equipped with chemical synthesis, biochemical technology and other talents who can complete route development, process docking and achievement transformation, satisfying  different cooperation needs. 合作模式Cooperation modes 为加速实现公司产业化、规范化、国际化发展，创造更大的社会效益，公司整合现有的技术、生产资源，引入战略合作者。我们愿意与您： In order to accelerate the realization of industrialization, standardization and internationalization, and create greater social benefits, the company integrates existing technology and production resources and introduces strategic partners. We would like to be with you. 1、公司作为原料药生产商，愿与制剂企业联合申报新药、仿制药批准文号； As an APIs manufacturer, the company is willing to jointly declare the approval number of new drugs and generic drugs with the pharmaceutical enterprises. 2、药品批文的转移或者转让； Transfer or transfer of pharmaceutical approval. 3、新产品验证批的生产； The production of new product verification batch. 4、相关产品及中间体的代工生产； The production of the related products and intermediates. 5、其他合作模式。 Other modes of cooperation.