In the Quality Control laboratory, the physical, chemical and microbiological analyses for all starting materials, finished products and stability samples and the controls of the manufacturing areas are carried out will the state-of-the-art analytical equipments under the supervision of the relevant departments and according to the cGMP rules.
The chemical and microbiological analyses of raw materials, packaging materials and finished products are carried out rigorously according to current pharmacopy methods. The methods used in the analysis of finished products are developed by the R&D department, and the validated analytical methods are put into application after method transfer is made to the Quality Control department. The ongoing stability program enables stability studies for different zones.
The equipment maintenance, calibration and qualification periods, the stability studies and all the analysis results for the Quality Control department are tracked via the ERP system.
