Quality Control is one of the key departments in any Pharma company
CHECKED IN THREE DIFFERENT STAGES
Raw material 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 is as per the guidelines then 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 approves.
In Process Sample analysis
The In Process Analysis will be done while the Product (Chemical or Formulation) is being Prepared/Manufactured
Finished Product analysis
Finished Product analysis will be done after the Product/material is manufactured
AIR HANDLING UNIT IN ALL AREA OF COMPANY
- 0.5 MICRON HEPA FILTER
- TEMERATURE 25 DEGREE CELCIUS
- RELATIVE HUMIDITY NOT LESS THAN 55
- RETURN/ SUPPLY CAPASITY
SEPARATE DM PLANT
- 250 LITRE/ HOUR CAPASITY
- SS 316 EL LOOP SYSTEM WITH SAMPLING POINT
