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In order to provide our customer with high purity and consistent reliable qualified intermediates and APIs,Chengdu Kaijie Bio-pharmaceutical Co.,Ltd has established an appropriate corporate organization.
We manufactures all our products on production lines compliant with these GMP requirements, and validation is implemented to establish the accuracy of the procedures and the control measures in all production processes. The existence of a drug substance production process makes it possible to achieve integrated quality control, from the GMP of drug substances to the packaging in the final process.
IPQC is carried out strictly for each product.In addition to strict quality control in each manufacturing process, the Quality Control (QC) Division in the QC Lab implements supervisory control. The Division monitors materials and products constantly on state-of-the-art analysis equipments as well as providing operational support to each department.
We also set up the Quality Assurance (QA) Division independently which separates from the Quality Control Division belonging to the Corporate Production Division. The QA Division provides additional supervision over the quality of all products, thereby guaranteeing the quality of our products. | 
