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Elixir Department: SOP for Cleaning of Utility Pipelines Used in Manufacturing – V 2.0

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Elixir Department: SOP for Cleaning of Utility Pipelines Used in Manufacturing – V 2.0

Standard Operating Procedure for Cleaning of Utility Pipelines Used in Elixir Manufacturing

Department Elixir Department
SOP No. SOP/ELX/113/2025
Supersedes SOP/ELX/113/2022
Page No. Page 1 of 8
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To establish a standard procedure for cleaning utility pipelines such as those used for Purified Water (PW), Steam, Compressed Air, and WFI lines in elixir manufacturing to ensure compliance with GMP and to prevent contamination or cross-contamination.

2. Scope

This SOP applies to all utility service pipelines connected to mixing vessels, transfer lines, and other manufacturing equipment within the Elixir Department.

3. Responsibilities

  • Maintenance Technician:
    • Perform cleaning operations and document activity.
  • Production Operator:
    • Support cleaning by ensuring lines are empty and isolated.
  • QA Officer:
    • Review cleaning records and verify cleanliness visually or via swab/rinse testing if applicable.
See also  Elixir Department: SOP for Identification of Holding Time and Conditions - V 2.0

4. Accountability

The Engineering Head is accountable for the proper execution and documentation of utility line cleaning, and ensuring their readiness for manufacturing.

5. Procedure

5.1 Identification of Pipelines

  1. Refer
to the pipeline schematic to identify relevant lines used for:
  • Purified Water (PW)
  • Water for Injection (WFI)
  • Steam (Clean/Plant)
  • Compressed Air
  • Tag lines requiring cleaning as per cleaning schedule or batch-specific instruction.
  • 5.2 Pre-Cleaning Checks

    1. Ensure isolation of the line from main utility source.
    2. Drain any residual product or utility from the pipeline.
    3. Wear appropriate PPE and display “Under Maintenance” signage in the area.

    5.3 Cleaning Methodology

    1. Purified Water/WFI Lines:
      • Flush with hot WFI or sanitizing agent (as applicable) followed by a purified water rinse.
      • Ensure final rinse has conductivity within acceptable limits.
    2. Steam Lines:
      • Flush with clean steam through all valves and condensate drain points.
      • Ensure condensate is clear and free from particulates or discoloration.
    3. Compressed Air Lines:
      • Purge using filtered compressed air.
      • Check for oil carryover and microbial load (if applicable).

    5.4 Post-Cleaning Verification

    1. Visually inspect all accessible ports, valves, and ends.
    2. Conduct rinse or swab test based on risk assessment and applicable validation protocol.
    3. Record cleaning parameters and sampling results in the Utility Cleaning Log (Annexure-1).

    5.5 Reconnection and Readiness

    1. Reconnect cleaned pipelines and test for integrity (leak check and pressure test).
    2. Label line as “CLEANED” and update status board in the production area.

    6. Abbreviations

    • SOP: Standard Operating Procedure
    • WFI: Water for Injection
    • PW: Purified Water
    • QA: Quality Assurance
    • PPE: Personal Protective Equipment

    7. Documents

    1. Utility Pipeline Cleaning Log (Annexure-1)
    2. Pipeline Layout and Identification Chart
    3. Cleaning Validation Protocol (if applicable)

    8. References

    • WHO TRS 1010 – Good Manufacturing Practices
    • ISPE Baseline Guide Vol. 6 – GEP for Utilities
    • 21 CFR Part 211.67 – Equipment and Utility Maintenance

    9. SOP Version

    Version: 2.0

    10. Approval Section

    Prepared By Checked By Approved By
    Signature
    Date
    Name
    Designation
    Department

    11. Annexures

    Annexure-1: Utility Pipeline Cleaning Log

    Date Line ID Utility Type Cleaning Method Final Rinse/Flush Result Cleaned By QA Verified
    11/04/2025 PW-07 Purified Water Hot WFI Flush Conductivity: 1.2 µS/cm Rajesh Kumar Sunita Reddy

    Revision History:

    Revision Date Revision No. Revision Details Reason for Revision Approved By
    01/01/2024 1.0 Initial SOP Release New SOP QA Head
    11/04/2025 2.0 Added cleaning verification and labeling Enhanced Compliance QA Head
    See also  Elixir Department: SOP for Transfer of Bulk Elixir to Storage Tank - V 2.0
    Elixers V 2.0 Tags:Elixir colorants, Elixir dosage form, Elixir filtration techniques, Elixir flavoring agents, Elixir formulation, Elixir GMP compliance, Elixir manufacturing process, Elixir manufacturing SOPs, Elixir packaging requirements, Elixir pharmacopoeial standards, Elixir preparation methods, Elixir preservatives, Elixir production equipment, Elixir quality control, Elixir regulatory guidelines, Elixir shelf life, Elixir stability testing, Elixir sterilization methods, Elixir storage conditions, Elixir sweetening agents, Elixir viscosity modifiers, Hydroalcoholic solutions, Medicated elixirs, Non-medicated elixirs, Pharmaceutical elixirs

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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
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    • Injectables
    • Liquid Orals
    • Liposome and Emulsion Formulations
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    • Lyophilized Products
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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

    • Aerosols V 2.0
    • Analytical Method Development V 2.0
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