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Ointments: SOP for Cleaning Utensils Used in Ointment Manufacturing – V 2.0

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SOP for Cleaning Utensils Used in Ointment Manufacturing – V 2.0

Procedure for Cleaning Utensils Used in Ointment Manufacturing

Department Production/Quality Assurance (QA)/Engineering
SOP No. SOP/Ointment/059
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 standardized method for cleaning utensils used in ointment manufacturing. Proper cleaning ensures removal of residues, prevents cross-contamination, and maintains compliance with Good Manufacturing Practices (GMP).

2. Scope

This SOP applies to all personnel involved in cleaning and maintaining utensils such as spatulas, mixing spoons, scrapers, beakers, and other tools used in ointment production.

3. Responsibilities

  • Production Supervisor: Ensures that cleaning is performed as per this SOP.
  • Machine Operator: Collects utensils and prepares them for cleaning.
  • Cleaning Personnel: Performs cleaning, sanitization, and drying of utensils.
  • Quality Assurance (QA) Personnel: Inspects and verifies cleaning effectiveness.
See also  Ointments: SOP for Evaluating Sensory Attributes of Ointments - V 2.0

4. Accountability

The Production and QA Managers are accountable for ensuring that utensil cleaning follows GMP standards and is properly documented.

5. Procedure

5.1 Pre-Cleaning Preparations

  • Ensure that all utensils used in the batch are collected for cleaning.
  • Wear appropriate Personal Protective Equipment (PPE), including gloves, masks, and aprons.
  • Ensure that all cleaning materials, including detergents and sanitizers, are available.
  • Inspect utensils for visible residues before starting the cleaning process.

5.2 Cleaning Process

5.2.1 Initial Rinsing

  • Rinse utensils
thoroughly with warm purified water to remove loose residues.
  • For heavily coated utensils, soak in warm water for 10-15 minutes.
  • 5.2.2 Detergent Cleaning

    • Prepare a cleaning solution using an approved detergent.
    • Use soft brushes or sponges to scrub utensils, ensuring all surfaces are cleaned.
    • Ensure cleaning reaches all crevices and edges of utensils.
    • Rinse with purified water to remove detergent residues.

    5.2.3 High-Pressure Rinsing

    • Use high-pressure purified water to rinse off any remaining detergent traces.
    • Repeat the rinsing process until all detergent residues are eliminated.

    5.2.4 Final Sanitization

    • Prepare a sanitizing solution (e.g., 70% ethanol or peracetic acid solution).
    • Immerse utensils in the sanitizing solution for at least 10 minutes.
    • Ensure complete coverage of all surfaces.
    • Remove utensils and drain excess sanitizer.

    5.3 Drying and Storage

    • Allow utensils to air dry in a controlled environment.
    • Store cleaned utensils in a designated clean storage area.
    • Ensure utensils are covered to prevent dust accumulation.

    5.4 Post-Cleaning Inspection

    • Conduct a visual inspection to ensure no residues remain.
    • Perform swab tests for microbial verification.
    • Record the results in the Cleaning Log.

    5.5 Documentation and Approval

    • Log all cleaning activities in the Cleaning Record.
    • QA personnel must review and approve the cleaned utensils before reuse.
    • Retain cleaning records for audits and compliance verification.

    6. Abbreviations

    • GMP – Good Manufacturing Practices
    • QA – Quality Assurance
    • QC – Quality Control
    • PPE – Personal Protective Equipment

    7. Documents

    • Cleaning Log (Annexure-1)
    • Cleaning Validation Report (Annexure-2)

    8. References

    • WHO GMP Guidelines for Pharmaceutical Manufacturing
    • 21 CFR Part 211 – Current Good Manufacturing Practices
    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients

    9. SOP Version

    Version 2.0

    10. Approval Section

    Prepared By Checked By Approved By
    Signature
    Date
    Name
    Designation
    Department

    11. Annexures

    Annexure-1: Cleaning Log

    Date Utensil Type Cleaning Solution Used Sanitization Agent Verified By
    01/02/2025 Spatula Detergent Solution 70% Ethanol QA Officer
    02/02/2025 Mixing Spoon Alkaline Cleaner Peracetic Acid QA Officer

    Annexure-2: Cleaning Validation Report

    Date Utensil Type Swab Test Result Microbial Limits Final Status Approved By
    01/02/2025 Spatula Pass Within Limit Approved QA Head
    02/02/2025 Mixing Spoon Pass Within Limit 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
    See also  Ointments: SOP for Validation of Homogenization - 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
    • 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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