The initial phase renovation will include two analytical labs and 8000 sq.-ft. of office space, and is scheduled to be complete by the end of September. The second phase includes additional clinical trial manufacturing (CTM) space for solid, semi-solid and sterile pharma products, packaging, labeling and distribution functions, and will be implemented at the beginning of 2015. Once the expansion is complete, the company expects to increase its CMC workforce and capacity by more than 50%.
“We’re excited that consistent growth over recent years is enabling us to expand capacity and service offerings,” said Dongmei Wang, Senior Vice President of CMC Services. “The infrastructure improvements will allow us to meet ever-thriving client demand for product development support, while adding efficiency gains to small scale CTM production and laboratory throughput.”
Frontage’s CMC service portfolio includes organic synthesis, formulation development, GMP analytical testing and GMP clinical trial material manufacturing, for all types of drug candidates ranging from novel, early phase projects to generic-equivalent and consumer care medications. Over the last ten years, Frontage developed oral solid, semi-solid, liquid and sterile dosage forms that have been evaluated in clinical research programs and commercialized in the US, EU and Asian markets by its clients.