Handling of Open-Damaged Containers in Warehouse
 1.0 Objective
To lay down a procedure for Handling of Open-Damaged Containers in Warehouse.
2.0 Scope
This Standard Operating Procedure is applicable for Handling of Open-Damaged Containers in
Warehouse to be followed at formulation plants of abc company.
3.0 Responsibility
3.1 Officer/Executive warehouse shall be responsible for handling of open-damaged containers in Warehouse.
3.2 Head Warehouse shall be responsible for implementation of this SOP.
3.3 Head QA or his designee shall be responsible for compliance of this SOP.
4.0 Abbreviations and Definitions
SOP : Standard Operating Procedure
QA : Quality Assurance
WH : Warehouse
HOD : Head of Department
5.0 Procedure
5.1 In case of damaged container warehouse person immediately inform to QA department in
duplicate notebook as per Annexure-1.
5.2 In case of packing materials, if boxes are in torn condition just transfer it into clean
polybag tie it and affix the proper label.
5.3 In case of Raw material in powder form, just keep it into the cleaned polybag and tie
it with cable tie and affix the proper label. In case of light resistant materials, keep it
into the black poly bag.
5.4 In case of Raw material in liquid form & Solvent items, intimate to QA department and follow
the instruction given by QA Department.
5.5 Precaution
5.5.1 Ensure that the open/damaged containers are kept separately.
6.0 Forms and Records
6.1 Intimation for Damaged Containers – Annexure-1
7.0 Distribution
7.1 Master Copy – Documentation Cell (Quality Assurance)
7.2 Controlled Copy – Warehouse Department.
8.0 History
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Revision Number Details For Change Reason for Revision00 New SOP NA - process validation protocol for methylcobalamin niacinamide and pyridoxine injection
validation protocol of sterility test sop for Analytical Method Transfer Protocol for hold time study of sterile garments sop for swab sampling for validation of clean surfaces cleaning validation maco and noel calculation formula sop for performance qualification for analyst Sop for Validation report for disinfectant efficacy Sop for Method validation report for bacterial endotoxin test Sop for method validation microbiology sterility testing sop for validation report for preservative efficacy test sop for Protocol cum report for efficacy qualification of uv light sop for validation protocol for uv light efficacy of dpb & laf sop for cleaning validation protocol tablet manufacturing equipment 
 
 
 
 sop for cleaning validation protocol ointment manufacturing equipmentconcurrent process validation for rabeprazole ec and domperidone sr capsules sop for Validation for cleaning procedure liquid injection sop for Validation for cleaning procedure dry powder injection Preparation Approval Control and Distribution of Master Formula Records calibration policy for equipment and instruments evaluation Sampling of Raw Materials questionnaire training evaluation questionnaire sop for approval of Contract Parties sop for Operation and Cleaning of Purified Water Generation System sop for Storage of Standard Weights sop for Dispensing of Raw Material Receipt of Excess RM/PM from Production sop for Dispatches of Finished Goods Cleaning of Dispensing and Sampling Area procedure for cleaning of dispensing tools 
 
- process validation protocol for methylcobalamin niacinamide and pyridoxine injection
