Since 1995, CNSHTH has been successfully providing fine chemicals, intermediates and active pharmaceutical ingredients (API) to clients worldwide. With global regulatory experiences and effective quality management, we are able to strategically ally with both API and finished product to meet our clients requirements. Tai Heng takes pride in providing high quality services with integrated professional sourcing, custom synthesis, contract manufacturing, technical support and distribution. Tai Hengs formulation division strives to solve full range of development issues and advance clients ANDA product development through FDA approval. Our current scope of work covers CGMP/ ANDA filing consulting, fully integrated formulation R&D services for generic drugs, which include preformulation, formulation, process development, engineering batch scale up, process validation, and ICH stability studies, etc. Our GMP-complied affiliated companies produce more than 80 kinds of APIs and drug products covering all kinds of digestive, cardiovascular, respiratory, and psychiatric diseases, and many of them have been approved by SFDA. In order to satisfy the ever stringent requirements of exporting APIs and pharmaceutical products to U.S. and Europe, our agent, ZenPharm International & Company, also provides worldwide top-class pharmaceutical services at best value, in full compliance with US FDA, and major EU regulatory agencies. Tai Heng is dedicated to produce more high quality products and is determined to establish long-term strategic partnerships with domestic and oversea pharmaceutical companies.