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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 Documentation of QC Test Results - 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.
See also  Ointments: SOP for Cleaning Heating Jacketed Vessels - V 2.0

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
See also  Ointments: SOP for Reviewing Trends in Stability Studies - V 2.0

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
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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