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Ointments: SOP for Preventing Air Entrapment During Mixing – V 2.0

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SOP for Preventing Air Entrapment During Mixing – V 2.0

Procedure for Preventing Air Entrapment During Mixing

Department Manufacturing/Production/Quality Assurance (QA)/Quality Control (QC)/Research and Development (R&D)
SOP No. SOP/Ointment/196
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 process for preventing air entrapment during the mixing of ointments. Air entrapment can lead to product instability, batch inconsistency, and reduced efficacy of the final formulation.

2. Scope

This SOP applies to all personnel involved in the handling, mixing, and quality control of ointment formulations in the Manufacturing, Production, Quality Assurance (QA), Quality Control (QC), and Research and Development (R&D) departments.

3. Responsibilities

  • Production Supervisor: Ensures adherence to anti-air entrapment procedures.
  • Process Operator: Monitors and controls mixing conditions to minimize air incorporation.
  • QA Officer: Verifies that mixing conditions meet process control guidelines.
  • QC Analyst: Conducts visual and microscopic analysis to detect air pockets.
  • Maintenance Engineer: Ensures vacuum systems and degassing equipment are functioning properly.
See also  Ointments: SOP for Homogeneity Testing at Different Stages - V 2.0

4. Accountability

The Production Manager is accountable for ensuring that all air entrapment prevention procedures comply with GMP, FDA, ICH, WHO, and company policies.

5. Procedure

5.1 Identifying Causes of Air Entrapment

  • Common causes of air entrapment in ointment mixing:
    • High-speed mixing without controlled vacuum application.
    • Rapid ingredient addition leading
to turbulence.
  • Improper positioning of mixing blades or agitators.
  • Insufficient deaeration time before filling.
  • Document identified risks in the **Air Entrapment Risk Assessment Log (Annexure-1).**
  • 5.2 Process Optimization to Minimize Air Entrapment

    • Adjust **mixing speeds based on batch size and viscosity**:
      • Initial blending: **50-100 RPM**
      • Homogenization: **200-400 RPM under vacuum**
      • Final blending: **30-60 RPM with slow agitation**
    • Introduce ingredients slowly to prevent excessive turbulence.
    • Use **vacuum mixing (negative pressure -0.8 bar) whenever possible.**
    • Document optimized conditions in the **Process Optimization Log (Annexure-2).**

    5.3 Deaeration Techniques

    • Use vacuum degassing systems to remove trapped air after mixing.
    • Ensure the product is **held under vacuum for 5-10 minutes** before filling.
    • Minimize manual interventions that may introduce air into the batch.
    • Record all deaeration process parameters in the **Deaeration Log (Annexure-3).**

    5.4 Post-Mixing Quality Control

    • Conduct **visual inspection** for air pockets or foaming.
    • Use **microscopic analysis** to confirm uniform consistency.
    • Verify bulk density and viscosity before proceeding to filling.
    • Record all test results in the **Quality Control Testing Log (Annexure-4).**

    6. Abbreviations

    • GMP – Good Manufacturing Practices
    • QA – Quality Assurance
    • QC – Quality Control
    • ICH – International Council for Harmonisation
    • FDA – Food and Drug Administration

    7. Documents

    • Air Entrapment Risk Assessment Log (Annexure-1)
    • Process Optimization Log (Annexure-2)
    • Deaeration Log (Annexure-3)
    • Quality Control Testing Log (Annexure-4)

    8. References

    • ICH Q8 – Pharmaceutical Development Guidelines
    • FDA Guidance on Mixing and Homogenization
    • WHO Guidelines on Manufacturing Process Control

    9. SOP Version

    Version 2.0

    10. Approval Section

    Prepared By Checked By Approved By
    Signature
    Date
    Name
    Designation
    Department

    11. Annexures

    Annexure-1: Air Entrapment Risk Assessment Log

    Date Batch No. Identified Risk Preventive Action QA Approval
    03/02/2025 OINT-5001 High-speed agitation Reduced RPM Approved

    Annexure-2: Process Optimization Log

    Date Batch No. Process Adjustment Outcome QA Approval
    03/02/2025 OINT-5001 Vacuum applied Entrapment reduced Approved

    Annexure-3: Deaeration Log

    Date Batch No. Vacuum Applied (bar) Deaeration Time (min) QA Approval
    04/02/2025 OINT-6001 -0.8 10 Approved

    Annexure-4: Quality Control Testing Log

    Date Batch No. Air Pockets Detected Bulk Density (g/mL) QA Approval
    04/02/2025 OINT-6001 No 1.02 Approved

    12. Revision History

    Revision Date Revision No. Details Reason Approved By
    03/02/2025 2.0 Expanded Air Entrapment Prevention Measures Regulatory Compliance QA Head
    01/01/2024 1.0 Initial SOP New SOP Implementation QA Head
    See also  Ointments: SOP for Lubricating Moving Parts of Equipment - 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
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    NEW! Revised SOPs – V 2.0

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    • BA-BE Studies V 2.0
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