The company has established cultivation bases for Citrus L, Sophorae Japonica, Phellodendri Chinensis based on requirements of GAP, which monitors each batch of raw materials for pesticide residues and heavy metals. The supply network of raw material established for decades is the guarantee for the quality and quantity of raw materials supplied by Chengdu Oukeang, so as the cornerstone of production and development.
Chengdu Okay Pharmaceutical Co., Ltd. is located in the Chengdu Food and Medicine Industrial Park which is in the southwest of Chengdu, Sichuan Province, and occupies an area with clean air and water of approximately 33,000 m2. Our factory is equipped with extracting capacity of 5000T/Year, Refining Capacity of 1000T/Year, two production capacity of 800T synthetic production lines, and a premixing workshop and finishing product workshop.
The factory is designed and constructed in accordance with CGMP requirements and is organized and operated in accordance with EUGMP requirements.
The company is equipped with an independent raw material warehouse, finished product warehouse and solvent/excipients warehouse with total area of totaling 4000m2. Configured and managed according to EUGMP requirements. Each warehouse has an individual area of Pending-inspection Zone, qualified product Zone and a non-qualified product warehouse. The finished product warehouse also has a return zone and a recall zone. All of the areas have temperature and humidity monitoring.
The factory has been ceritified including EUGMP、CGMP、ISO9001-2015、ISO22000、HACCP、KOSHER、HALAL、SC. Food and drug production and operation shall be carried out according to the corresponding quality management system.
The main products are registered in CEP, DMF, ND, etc. in Europe, America and China.
The company draft and formulate the unit for the international business standards of hesperidin from Citrus L series, rutin from Sophorae Japonica series and quercetin.
800m2 QC center can carry out accurate detection independently according to EP, USP, BP, JP, CP and other standards, and strictly be followed the safety management requirements of GxP computer system.
