In Quality Control laboratories; state-of-the-art analytic equipment are used for physical, chemical and microbiological analyses of all the starting materials, finished products and stability samples, environmental controls of production areas are carried out in accordance with cGMP regulations.

Chemical and microbiological analyses of raw materials, packaging materials and finished products are conducted meticulously in compliance with current pharmacopeia methods. Methods used in finished product analyses are developed by the R&D department; validated analytical methods are put into effect after being transferred to the Quality Control department. Stability studies for different zones are performed within the ongoing stability programme.

Equipment maintenance, calibration and qualification periods, stability studies and all of the analysis results of the quality control department are tracked through the ERP system.