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Ointments: SOP for Transferring Ointments to Filling Machines – V 2.0

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SOP for Transferring Ointments to Filling Machines – V 2.0

Procedure for Transferring Ointments to Filling Machines

Department Production/Quality Assurance (QA)/Engineering
SOP No. SOP/Ointment/027
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 establish a standardized process for transferring ointments from the manufacturing vessel to the filling machine. Proper transfer ensures product integrity, prevents contamination, and maintains consistency in filling operations.

2. Scope

This SOP applies to all personnel involved in the transfer of ointments from storage tanks or processing vessels to automatic or semi-automatic filling machines in the production area.

3. Responsibilities

  • Production Supervisor: Oversees the transfer process and ensures compliance with SOP guidelines.
  • Machine Operator: Operates and monitors the transfer equipment.
  • Quality Assurance (QA) Personnel: Verifies product integrity and ensures compliance with GMP standards.
  • Engineering Technician: Maintains and troubleshoots the transfer system.
See also  Ointments: SOP for Preventing Contamination at Each Stage - V 2.0

4. Accountability

The Production and QA Managers are accountable for ensuring that the ointment transfer process is conducted as per GMP standards and properly documented.

5. Procedure

5.1 Pre-Transfer Preparations

  • Ensure that the filling machine, transfer hoses, and storage tanks are clean and sanitized.
  • Verify that the ointment batch has been approved for filling by the QA department.
  • Check the temperature of the ointment to ensure it is within the
specified range for transfer.
  • Ensure that all valves, pumps, and transfer lines are correctly assembled.
  • 5.2 Selection of Transfer Method

    • Gravity Transfer: Used for small-scale manual filling.
    • Pneumatic Transfer: Utilizes compressed air to push the product through transfer lines.
    • Positive Displacement Pump Transfer: Ensures uniform flow to the filling machine.

    5.3 Transferring the Ointment

    • Connect the transfer hoses securely to prevent leaks.
    • Activate the transfer system and monitor the flow rate.
    • Ensure there are no air bubbles or interruptions in the transfer process.
    • Maintain constant agitation (if required) to prevent phase separation.

    5.4 Monitoring During Transfer

    • Observe the transfer for any signs of clogging or foaming.
    • Ensure that all connections remain sealed to avoid contamination.
    • Check that the transfer rate is consistent with the filling machine’s capacity.

    5.5 Completion of Transfer

    • Shut off the transfer system once the required volume has been transferred.
    • Disconnect and flush the transfer lines with an approved cleaning solution.
    • Perform a final weight verification of the transferred batch.

    5.6 Documentation and Approval

    • Record all process parameters in the Ointment Transfer Log.
    • QA must verify and approve the transferred batch before filling begins.
    • Label the filled machine hopper as “Ready for Filling.”

    6. Abbreviations

    • GMP – Good Manufacturing Practices
    • QA – Quality Assurance
    • R&D – Research and Development
    • BMR – Batch Manufacturing Record

    7. Documents

    • Ointment Transfer Log (Annexure-1)
    • In-Process Quality Control Report (Annexure-2)

    8. References

    • WHO GMP Guidelines for Pharmaceutical Manufacturing
    • 21 CFR Part 211 – Current Good Manufacturing Practices
    • Equipment Manufacturer Guidelines

    9. SOP Version

    Version 2.0

    10. Approval Section

    Prepared By Checked By Approved By
    Signature
    Date
    Name
    Designation
    Department

    11. Annexures

    Annexure-1: Ointment Transfer Log

    Date Batch Number Transfer Method Temperature (°C) Transfer Time (Min) Verified By
    01/02/2025 SOP/Ointment/001 Pneumatic 55°C 20 QA Officer
    02/02/2025 SOP/Ointment/002 Gravity 50°C 15 QA Officer

    Annexure-2: In-Process Quality Control Report

    Date Batch Number Test Parameter Specification Result Final Status
    01/02/2025 SOP/Ointment/001 Temperature 50-60°C 55°C Pass
    02/02/2025 SOP/Ointment/002 Transfer Efficiency ≥98% 99% Pass

    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
    See also  Ointments: SOP for Cleaning and Re-Starting Manufacturing Lines - V 2.0
    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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