Identification of deviation
Issuance
of the deviation control form from
QA department (with unique deviation number)
Fill up
the deviation control form with proper
justification by the concern department
Comments
of other department
(If any impact on their system due to deviation)
Review
and investigation of the deviation
by QA designee
(Categorize the deviation)
Evaluation of deviation by Head QA
Approval or rejection of the deviation
Proper
corrective and preventive action(CAPA) based
on the investigation
and route cause analysis
Implementation of Corrective and preventive action(CAPA) if required
Closing
of deviation
|
Flow chart for Deviation control Procedure in Pharmaceutical Industry
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment