Since 2005, Tai Heng has been a cGMP compliance CMC development company fully in compliance with US cGMP regulations. We have more than a dozen API DMFs and formulation dossiers either approved or pending approval by US FDA, through licensing or partnership with US generic companies. In addition to our ever-expanding generic drug portfolio, we are currently offering our turn-key CMC services to later stage drug development companies where cGMP becomes mandatory, from API synthesis to Formulated Products. We also provide services for product lifecycle improvement to expand product value and stay in compliance with most stringent government regulations. Tai Heng maintains a US FDA inspected Kilolab & Formulation Development Center in Shanghai, China, and business office in Orange County, California, USA.