Tai Heng Industry Co., Ltd. is one of the fastest growing private pharmaceutical companies in China. We established in 1995, and engaged in the Active Pharmaceutical Ingredients (APIs), Formulation Dossier Developments and Contract Analysis Services for customers worldwide.

With our excellent development, regulatory and portfolio management expertise, Tai Heng currently has more than 15 DMFs (Drug Master Files) active with US FDA and over 10 formulation projects in various stage of regulatory approval across the global. All of our research and commercial manufacturing is in compliance with the most stringent US FDA and ICH regulations.

Tai Heng provides the best pharmaceutical solution on Chemical Synthesis (customized synthesis, cGMP manufacturing), Analytical Method Development, Formulation Development and Regulatory Services.