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Ointments: SOP for Water Content Analysis in Ointments – V 2.0

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SOP for Water Content Analysis in Ointments – V 2.0

Procedure for Water Content Analysis in Ointments

Department Quality Control (QC)/Quality Assurance (QA)/Analytical Development
SOP No. SOP/Ointment/067
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 method for determining the water content in ointments. Water content is a critical parameter that affects product stability, texture, microbial growth, and compliance with product specifications.

2. Scope

This SOP applies to all personnel in the Quality Control (QC), Quality Assurance (QA), and Analytical Development departments responsible for conducting water content analysis in ointments during formulation development, in-process control, and final batch release.

3. Responsibilities

  • Quality Control Analyst: Conducts water content analysis and records results.
  • Quality Assurance Personnel: Reviews and approves test results.
  • Production Supervisor: Ensures that ointment batches conform to water content specifications.
  • R&D and Analytical Development Team: Evaluates formulation modifications based on water content test results.
See also  Ointments: SOP for Ensuring Batch Uniformity in Ointments - V 2.0

4. Accountability

The QC, Analytical Development, and QA Managers are accountable for ensuring that water content analysis is conducted accurately and documented as per regulatory and GMP standards.

5. Procedure

5.1 Equipment and Materials

  • Karl Fischer Titrator
  • Oven (for Loss on Drying Method, if applicable)
  • Weighing balance (calibrated)
  • Titrant solution (Karl Fischer reagent)
  • Solvent (e.g., methanol, formamide)
  • Disposable pipettes
  • Glassware (volumetric flasks,
beakers)
  • Data recording sheets
  • 5.2 Sample Preparation

    • Weigh an appropriate quantity of the ointment sample (e.g., 0.5 g – 1 g).
    • Transfer into a suitable solvent to dissolve the sample.
    • Ensure complete homogenization before analysis.

    5.3 Water Content Determination Methods

    5.3.1 Karl Fischer Titration Method

    • Ensure the Karl Fischer Titrator is calibrated and filled with reagent.
    • Prepare the sample solution in an appropriate solvent.
    • Inject the sample into the Karl Fischer Titrator.
    • Allow titration until the endpoint is reached.
    • Record the water content percentage displayed by the instrument.

    5.3.2 Loss on Drying (LOD) Method (If Applicable)

    • Weigh the sample in a pre-weighed moisture dish.
    • Place the dish in an oven at 105°C for 2 hours.
    • Remove and allow to cool in a desiccator.
    • Weigh again and calculate the water content using:
    • Water Content (%) = [(Initial Weight – Final Weight) / Initial Weight] × 100

    5.4 Acceptance Criteria

    • Water content should be within the specified range (e.g., 1% – 5% depending on the formulation).
    • Deviations from specifications require investigation and possible batch reprocessing.

    5.5 Documentation

    • Record all water content analysis results in the Water Content Test Log.
    • Document instrument calibration details and method parameters.
    • QA personnel must review and approve results before batch release.

    6. Abbreviations

    • GMP – Good Manufacturing Practices
    • QA – Quality Assurance
    • QC – Quality Control
    • LOD – Loss on Drying
    • KF – Karl Fischer Titration

    7. Documents

    • Water Content Test Log (Annexure-1)
    • Ointment Batch Water Content Report (Annexure-2)

    8. References

    • WHO GMP Guidelines for Pharmaceutical Manufacturing
    • USP <921> – Water Determination
    • ICH Q2 (R1) – Validation of Analytical Procedures

    9. SOP Version

    Version 2.0

    10. Approval Section

    Prepared By Checked By Approved By
    Signature
    Date
    Name
    Designation
    Department

    11. Annexures

    Annexure-1: Water Content Test Log

    Date Batch Number Sample Weight (g) Water Content (%) Result Verified By
    01/02/2025 OINT-101 0.5 2.5% Pass QA Officer
    02/02/2025 OINT-102 0.5 3.1% Pass QA Officer

    Annexure-2: Ointment Batch Water Content Report

    Date Batch Number Test Method Acceptance Criteria Result Final Status Approved By
    01/02/2025 OINT-101 Karl Fischer 1% – 5% 2.5% Approved QA Head
    02/02/2025 OINT-102 Loss on Drying 1% – 5% 3.1% Approved 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
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    • Microbiology Testing
    • Nanoparticle Formulation
    • Nasal Spray Formulations
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    • Ointments
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    • 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

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    • 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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