SOP for Additional Packing Materials Request using format and ERP

👤 Written by: Naresh Bhakar
Founder | Pharmaceutical Professional

Reviewed by: Pankaj Sharma - Quality Control Specialist
Reviewed for Quality Control accuracy, laboratory practices, and technical relevance

📅 Last Updated: June 7, 2026
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1.0 OBJECTIVE: To define a procedure for requesting additional packing material in packaging department in pharmaceuticals

2.0 SCOPE: This SOP is applicable to the Production Department for raising additional packing material requests.

3.0 RESPONSIBILITY

Officer / Executive – Responsible for following this SOP.
Head Production: to ensure compliance with this procedure.
Head Quality Assurance: Ensure compliance and authorization of additional material requests.

4.0 DEFINITION(S)
NA

5.0 PROCEDURE for Additional Packing Materials Request:
5.1 On shortage of material from standard issue quantity, production operator/officer raises the additional packing material requisition using the standard format provided in the Batch Packing Record (BPR) or using the ERP.

5.2 Fill in the product details along with required quantity to get approval from production and QA department before making entry in ERP.

Follow the steps below to raise the request in ERP:

5.2.1 Open the ERP system using your credentials.

Pharma ERP work order deviated issue request module displaying additional packing material request process, manufacturing transaction management, inventory control, and production workflow in pharmaceutical manufacturing

5.2.2 Open the “WORK ORDER DEVIATED ISSUE REQUEST” module using the ERP system.

5.2.3 Now, click on the “ADD NEW” option displayed on the module screen.

5.2.4 On the new screen, enter the product details “WORK ORDER“, then navigate to the WORK ORDER DETAILS column as shown on the screen.

Pharma ERP work order deviated issue request screen showing additional packing material request entry form with work order details, item code, batch information, department code, production data, and approval fields in a pharmaceutical manufacturing ERP system

5.2.5 After entering the Work Order, a new screen with Work Order Details will open.

5.2.6 Fill in the following fields using the available popup options:

ERP screen showing the procedure for additional packing materials request in a pharmaceutical manufacturing system, including work order deviated issue request form, item code entry, quantity details, QC requirement selection, and approval workflow for GMP-compliant batch packing operations
  • Item
  • Depratment
  • Dept code
  • Remark
  • Item code
  • Quantity

Note: Make sure approved quantity is available for use.

If more than one material item needs to be requested, use the “ADD NEW” option to add additional line items. Once all entries are complete, save the request.

5.3 Thoroughly recheck all entries and send additional packing material requests to the Stores Department.

5.4 On receiving the material, Check issued quantity against the requisition slip.

5.5 Transfer the received additional packing material to the designated Primary Packing Area or Secondary Packing Area, as applicable.

6.0 ABBREVIATIONS

AbbreviationFull Form
BPRBatch Packing Record
QAQuality Assurance
SOPStandard Operating Procedure
ERPEnterprise Resource Planning

7.0 REFERENCES
NA

8.0 ANNEXURES
Nil (Format included)

Additional Material Request Form format used in pharmaceutical manufacturing for GMP-controlled material issuance, batch reconciliation, production verification, and QA approval.

9.0 DISTRIBUTION

Copy TypeDepartment
Master CopyQuality Assurance
Controlled CopyProduction Department, Quality Assurance
Reference Copy Production Department (2 copies)

Questionnaire for Indenting of additional packing material

Questionnaire for Indenting of extra packing material

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