上海泰亨实业有限公司是一家符合符合美国cGMP要求的制药企业,从事原料药的生产和后续制剂的开发。泰亨公司成立于1995年,至今已成功申报了10余个USDMF文件,为欧美市场以及其他国内外客户供应品质优良的产品,并在2009年3月经历了美国FDA的现场检查。多年以来,泰亨始终致力于为全球医药行业提供优秀的服务!Tai Heng Industry Co., Ltd. is a cGMP-complied pharmaceutical companyspecializing in the manufacture of API and formulation development.Founded in 1995, Tai Heng has registered over ten DMFs with the U.S. FDAand has been providing quality products and services for U.S. &European customers and domestic companies. Our API manufacturing sitewas inspected by the FDA in March 2009. For years, we have beendedicated to serving the pharmaceutical industry worldwide as a reliableAPI manufacturer and formulation developer.