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

With state-of-the art development, regulatory, and portfolio management expertise, Tai Heng currently has over 15 DMFs (Drug Master Files) active with U.S. FDA and another 10 global formulation projects in various stages of regulatory approval around the world. All research and commercial manufacturing is in compliance with mandatory U.S. FDA and ICH regulations.

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