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Ointments: SOP for Barcoding and Serialization in Packaging – V 2.0

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SOP for Barcoding and Serialization in Packaging – V 2.0

Procedure for Barcoding and Serialization in Packaging

Department Packaging/Quality Assurance (QA)/Production
SOP No. SOP/Ointment/097
Supersedes V 1.0
Page No. Page X of Y
Issue Date [Insert Issue Date]
Effective Date [Insert Effective Date]
Review Date [Insert Review Date]

1. Purpose

The purpose of this Standard Operating Procedure (SOP) is to define the procedure for barcoding and serialization in the packaging of ointments. This ensures compliance with Good Manufacturing Practices (GMP), regulatory traceability, and product authenticity.

2. Scope

This SOP applies to all personnel in the Packaging, Quality Assurance (QA), and Production departments responsible for generating, printing, verifying, and recording barcodes and serial numbers during packaging operations.

3. Responsibilities

  • Packaging Operator: Prints and applies barcodes and serial numbers as per batch packaging record (BPR).
  • Packaging Supervisor: Monitors barcode and serialization processes and ensures data accuracy.
  • Quality Assurance (QA) Officer: Verifies barcode readability and serialization records.
  • IT/Data Management Team: Maintains barcode and serialization database.
  • QA Manager: Approves barcoded and serialized batches before distribution.
See also  Ointments: SOP for Conducting Preventive Maintenance on Validated Equipment - V 2.0

4. Accountability

The QA and Packaging Managers are accountable for ensuring barcoding and serialization processes meet GMP and regulatory requirements.

5. Procedure

5.1 Pre-Serialization and Barcode Setup

  • Ensure that the barcode printing system is calibrated and functioning correctly.
  • Verify the barcode format and serialization sequence according to regulatory requirements.
  • Ensure that the correct batch number, expiry date, and manufacturing date are
set in the system.

5.2 Barcode and Serial Number Printing

  • Print barcodes and serial numbers on each unit, carton, and shipping case as per batch specifications.
  • Ensure correct label alignment to prevent scanning issues.
  • Use machine-readable codes (e.g., GS1 DataMatrix, QR codes) as per regulatory guidelines.

5.3 Verification of Barcodes and Serial Numbers

  • Perform random sampling of printed barcodes to check legibility and accuracy.
  • Use barcode scanners to verify that all barcodes are readable.
  • Confirm that serialization follows a unique, non-repetitive sequence.

5.4 Data Recording and Traceability

  • Record all generated serial numbers in the Serialization Log.
  • Ensure batch-specific barcode data is stored in the serialization database.
  • Verify that serialization data is linked to the batch packaging record (BPR).

5.5 Handling of Barcode and Serialization Errors

  • Identify and segregate packaging units with unreadable or incorrect barcodes.
  • Reprint or reapply barcodes for defective units.
  • Document all errors and corrective actions taken.

5.6 Final QA Approval

  • QA must perform a final inspection of barcode integrity and serialization compliance.
  • Ensure that serialized data is reconciled before batch release.
  • Approve the final packaged batch for shipment.

6. Abbreviations

  • GMP – Good Manufacturing Practices
  • QA – Quality Assurance
  • QC – Quality Control
  • BPR – Batch Packaging Record
  • GS1 – Global Standards for Serialization

7. Documents

  • Serialization Log (Annexure-1)
  • Barcode Verification Report (Annexure-2)

8. References

  • WHO GMP Guidelines for Pharmaceutical Manufacturing
  • ICH Q10 – Pharmaceutical Quality System
  • GS1 Guidelines for Serialization

9. SOP Version

Version 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Serialization Log

Date Batch Number Serialization Format Starting Serial Number Ending Serial Number Verified By
01/02/2025 OINT-101 GS1 DataMatrix 1000001 1000500 QA Officer
01/02/2025 OINT-102 QR Code 2000001 2000500 QA Officer

Annexure-2: Barcode Verification Report

Date Batch Number Barcode Type Scanned (Yes/No) Defective Units Corrective Action Verified By
01/02/2025 OINT-101 GS1 DataMatrix Yes 2 Reprinted QA Officer
02/02/2025 OINT-102 QR Code Yes 1 Reprinted QA Officer

12. Revision History:

Revision Date Revision No. Details of Revision Reason for Revision Approved By
01/01/2024 1.0 Initial Version New SOP QA Head
01/02/2025 2.0 Updated SOP Format Standardization of Document QA Head
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Ointments V 2.0 Tags:Ointment application SOP, Ointment batch record SOP, Ointment compounding SOP, Ointment dispensing SOP, Ointment filling SOP, Ointment formulation SOP, Ointment manufacturing SOP, Ointment microbiological testing SOP, Ointment pH testing SOP, Ointment production SOP, Ointment quality control SOP, Ointment stability study SOP, Pharmaceutical ointment SOP, SOP for ointment homogenization, SOP for ointment labeling, SOP for ointment mixing, SOP for ointment packaging, SOP for ointment preparation, SOP for ointment raw material testing, SOP for ointment shelf-life determination, SOP for ointment stability testing, SOP for ointment sterilization, SOP for ointment storage, SOP for ointment testing, SOP for ointment viscosity testing

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Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

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NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

New Publication: A must for All.

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