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Ointments: SOP for Initial Heating Stage in Ointment Manufacturing – V 2.0

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SOP for Initial Heating Stage in Ointment Manufacturing – V 2.0

Procedure for Initial Heating Stage in Ointment Manufacturing

Department Production/Quality Assurance (QA)/Engineering
SOP No. SOP/Ointment/031
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 a systematic approach for the initial heating stage in ointment manufacturing. Proper heating ensures uniform melting of base materials, enhances ingredient solubility, and maintains product consistency.

2. Scope

This SOP applies to all personnel responsible for the heating of waxes, oils, emulsifiers, and other base materials in the ointment manufacturing process.

3. Responsibilities

  • Production Supervisor: Ensures adherence to heating parameters and safety protocols.
  • Machine Operator: Monitors temperature, heating duration, and mixing conditions.
  • QA Personnel: Verifies temperature accuracy and compliance with GMP requirements.
  • Engineering Technician: Ensures heating system functionality and calibration.
See also  Ointments: SOP for Incorporating Excipients in Ointment Formulations - V 2.0

4. Accountability

The Production and QA Managers are accountable for ensuring that the initial heating stage is performed as per GMP and documented correctly.

5. Procedure

5.1 Pre-Heating Preparations

  • Ensure the heating vessel is clean and dry.
  • Check the availability of required base materials as per the Batch Manufacturing Record (BMR).
  • Verify the calibration status of temperature sensors.

5.2 Loading of Base Materials

  • Weigh and transfer waxes, oils, and emulsifiers into the heating vessel.
  • Use a slow agitation setting to ensure
uniform heat distribution.
  • Ensure no contamination occurs during material transfer.
  • 5.3 Heating Process

    • Gradually increase the temperature to the specified range (e.g., 60°C–80°C).
    • Monitor heating rate to prevent thermal degradation.
    • Ensure constant stirring to maintain homogeneity.

    5.4 Monitoring During Heating

    • Check temperature at regular intervals using a calibrated thermometer.
    • Observe for uniform melting without residue formation.
    • Ensure no overheating or burning occurs.

    5.5 Completion of Heating Stage

    • Confirm complete melting of all ingredients.
    • Hold the mixture at the final heating temperature for the required duration.
    • Record final temperature and time before proceeding to emulsification.

    5.6 Documentation and Approval

    • Record heating parameters in the Heating Log.
    • QA must verify and approve the batch before further processing.
    • Label the batch as “Melted and Ready for Mixing.”

    6. Abbreviations

    • GMP – Good Manufacturing Practices
    • QA – Quality Assurance
    • QC – Quality Control
    • BMR – Batch Manufacturing Record

    7. Documents

    • Heating Log (Annexure-1)
    • Temperature Monitoring 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: Heating Log

    Date Batch Number Material Name Heating Temperature (°C) Time (Min) Verified By
    01/02/2025 SOP/Ointment/001 White Petrolatum 70°C 30 QA Officer
    02/02/2025 SOP/Ointment/002 Beeswax 75°C 40 QA Officer

    Annexure-2: Temperature Monitoring Report

    Date Batch Number Material Name Initial Temp (°C) Final Temp (°C) Approved By
    01/02/2025 SOP/Ointment/001 White Petrolatum 20°C 70°C QA Head
    02/02/2025 SOP/Ointment/002 Beeswax 22°C 75°C QA Head

    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 Conducting Swab Sampling for Residue Testing - V 2.0
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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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