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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 inspection for the facility of Hydrochlorothiazide and Doxycycline Hyclate in Oct.2005.
Received CEP certificate for Hydrochlorothiazide in Nov.2006.
Approved by EU GMP for Doxycycline Tablets,Doxycycline Capsule and Folic Acid Tablets in 2007.
Passed FDA's latest inspection for the facility of Hydrochlorothiazide and Doxycycline Hyclate in Jun.2009.
Approved by European GMP for APIs in 2010.
Approved by EU GMP for Doxycycline Tablets, Doxycycline Capsule and Folic Acid Tablets in 2010.