Quality Control is one of the key departments in any Pharma company. The Quality will be checked in three different stages: Raw material analysis, In Process Sample analysis, Finished Product analysis. Once the raw material enters the factory premises and before going to the Stores department the Quality of the material will be checked by QC department. If the quality meets the guidelines, the QC department approves the raw material. This is called Raw material analysis. The concerned QC chemist will perform the basic duties, and the Group leader or Manager will approve. The in-Process Analysis will be conducted while the Product (Chemical or Formulation) is being prepared and manufactured. Finished Product analysis will be done after the Product is manufactured.