: QC systems in Pharm Asia drug monitor and maintain quality of entire operations and the processes at every stage. It is involved in group of activities concerned with specifications, documentation, release procedures, sampling, destruction, and analysis at key points in the production unit, interpretation of data and recommendations for action. Q.C. is independent from production and is responsible only to the top-level management. It is involved in microbiological activities concerned with standard testing procedure, documentation, sampling, media preparation, microbial limit test, test for pathogens, antibiotic assay, environmental monitoring etc. all test are performed in validated microbiology lab.. The unit is strongly supported by the quality division equipped with modern instruments like HPLC, stability chamber, Spectrometer, & Laminar Air Flow, Antibiotic zone reader, Digital Autoclave, Incubators other sophisticated equipments to controland ensure best quality of the product as per cGMP requirement.
