Tai Heng provides the best pharmaceutical solutions for Chemical Synthesis (customized synthesis, cGMP manufacturing), Analytical Method Development, Formulation Development, and Regulatory Services. With state-of-the art development, regulatory, and portfolio management expertise, we currently has over 15 DMFs 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.