sop on Issue of additional Raw and Packaging materials
- Objective:To lay down a procedure for issuing additional raw and packing material to the Production Department.
- Scope:This SOP is applicable for issuing additional raw and packing material to the Production Department at (Pharmaceutical Company Name).
- Responsibility:Warehouse personnel shall be responsible for issuing additional raw and packing material to the Production Department.
- Accountability: Concerned Department Head and QA Head shall be accountable for implementation of this SOP.
- Abbreviations and Definitions
QA :Quality Assurance
SOP :Standard Operating Procedure
- Procedure:
- The Additional Raw and Packing material shall be issued to production department under following circumstances:-
- On line Rejection.
- Re-Processing.
- Spillage and Wastages of Materials during transit and production.
- Production Department shall raise a requisition in the form of “Supplementary Slip in Duplicate for Raw and Packing Materials”.
- This Requisition shall be authorized by Head-QA after investigating the Requirement of additional material.
- After receiving the “Supplementary Slip for Raw and Packing Materials” from production department, material should be dispensed as per its SOP.
- While dispensing the additional material, it shall be assured that the material being issued is approved.
- The detail of the additional materials issued shall be recorded in “Supplementary Slip for Raw and packing Materials”.
- Keep the store copy for Record and hand over the production copy to production department.
- Record the issue detail in stock ledger.
- The Additional Raw and Packing material shall be issued to production department under following circumstances:-
- Forms and Records: Not Applicable.
- Distribution
- Master copy – Quality Assurance
- Controlled copies – Quality Assurance & Production
- History
Date | Revision Number | Reason for Revision |
– | – | New SOP |
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