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Changzhou Pharmaceutical Factory (CPF) is a leading pharmaceutical manufacturer of API's , finished formulations in China. Located in Changzhou, Jiangsu province and has a history of more than half a century. It covers an area of 110,000m2 and employs 1000 staffs, including more than 300 technicians with different specialties.Specialized in producing cardiovascular pharmaceuticals and medicines, every year the output of 30 kind of API's is more than 3000 tons and that of 120 kind of finished formulations is more than 8,000 million tablets.
　 The factory carries out management and production as per GMP requirements. It imported production equipments and test instruments from America, Europe, Japan etc. The products are exported to over 50 countries. With “Credit, Contract-Observed, Quality First and Customer Priority” as its motto, CPF is willing to cooperate with friends in the whole world.

CPF is established in Changzhou city in the year of 1949.
Moved from the Center of Changzhou city to the present address in 1958.
As a basement of APIs' production, CPF was administered by the central government directly in 1964.
Our API, Hydrochlorothiazide was approved by U.S.FDA in 1984.
Awarded as State Class II Enterprise by the government in 1988.
Our API, Doxycycline Hyclate was approved by U. S.FDA in 1992.
Awarded as High Technology Enterprise by the government in 1994, 1997 and 2004 respectively.
Reformed as company limited from state-owned enterprise in 2001.
Approved by Chinese GMP for finished dosages in 2002.
Approved by Chinese GMP for APIs in 2004.
Passed FDA's latest inspection for the facility of Hydrochlorothiazide and Doxycycline Hyclate in Oct.,2005