Importance(Requirement) of Deviation in Pharmaceutical industry

Following are the reason why deviation should documented in Pharmaceutical industry:

-To document the any abnormal activity happen in plan, as it can be reference for the future.
 

-To reduce the adverse impact on the quality of the product. 

-To prevent the re occurrence of the deviation. 

-Repeated deviation can be identified, If based on the repeat deviation any requirement of change in present situation it can be identified and improved (E.g. : change in equipment of any part of the equipment).

-Route cause analysis (RCA) can be find by the proper identification and documentation of deviation. 

-Proper Corrective action and preventive action(CAPA) can be taken by finding the exact reason of the deviation. 

-To identify the risk during the manufacturing activity accordingly risk analysis can be performed 

-By proper risk analysis risk can be reduced.