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Ointments: SOP for Maintaining Scraper Blade Mixers – V 2.0

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SOP for Maintaining Scraper Blade Mixers – V 2.0

Procedure for Maintaining Scraper Blade Mixers

Department Production/Engineering/Quality Assurance (QA)
SOP No. SOP/Ointment/044
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 establish a systematic approach for maintaining scraper blade mixers used in ointment production. Proper maintenance ensures efficient mixing, prevents contamination, and extends equipment lifespan.

2. Scope

This SOP applies to all personnel responsible for the operation, cleaning, and maintenance of scraper blade mixers in the manufacturing facility.

3. Responsibilities

  • Production Supervisor: Ensures scraper blade mixers are maintained as per schedule.
  • Machine Operator: Performs routine checks and identifies maintenance needs.
  • Quality Assurance (QA) Personnel: Verifies cleanliness and operational efficiency.
  • Engineering Technician: Conducts preventive and corrective maintenance.
See also  Ointments: SOP for Conducting QA Audits in Ointment Manufacturing - V 2.0

4. Accountability

The Production and QA Managers are accountable for ensuring that scraper blade mixer maintenance follows GMP standards and is properly documented.

5. Procedure

5.1 Pre-Use Inspection

  • Check that the scraper blade mixer is clean and free of residue.
  • Ensure that the blade is securely attached and shows no signs of wear.
  • Verify that the mixing vessel is properly aligned with the scraper blade.

5.2 Routine Maintenance

  • Lubricate moving parts to prevent friction-related wear.
  • Inspect and tighten fasteners to secure the blade.
  • Ensure the scraper blade does not have cracks or
sharp edges that may contaminate the batch.
  • Monitor motor function and check for unusual noises during operation.
  • 5.3 Cleaning After Each Batch

    • Disassemble scraper blade components following manufacturer guidelines.
    • Wash the blade, mixing vessel, and surrounding areas with an approved cleaning agent.
    • Rinse thoroughly with purified water to remove any residues.
    • Sanitize all parts and reassemble before the next use.

    5.4 Preventive Maintenance Schedule

    • Perform deep cleaning and sanitization weekly.
    • Conduct blade wear analysis monthly.
    • Replace worn-out scraper blades as per the manufacturer’s recommendation.
    • Calibrate the scraper blade mixer every six months.

    5.5 Handling Equipment Failures

    • Stop production immediately if any mechanical issue is detected.
    • Document the fault and notify the Engineering department.
    • Ensure necessary repairs or replacements are conducted before resuming operation.

    5.6 Documentation and Approval

    • Record all maintenance activities in the Equipment Maintenance Log.
    • QA must review and approve maintenance records.
    • Retain maintenance records for audits and inspections.

    6. Abbreviations

    • GMP – Good Manufacturing Practices
    • QA – Quality Assurance
    • QC – Quality Control
    • BMR – Batch Manufacturing Record
    • RPM – Revolutions Per Minute

    7. Documents

    • Equipment Maintenance Log (Annexure-1)
    • Cleaning and Sanitization Log (Annexure-2)

    8. References

    • WHO GMP Guidelines for Pharmaceutical Manufacturing
    • 21 CFR Part 211 – Current Good Manufacturing Practices
    • Equipment Manufacturer Guidelines

    9. SOP Version

    Version 2.0

    10. Approval Section

    Prepared By Checked By Approved By
    Signature
    Date
    Name
    Designation
    Department

    11. Annexures

    Annexure-1: Equipment Maintenance Log

    Date Machine ID Maintenance Type Action Taken Verified By
    01/02/2025 SM-101 Routine Inspection Lubricated bearings QA Officer
    02/02/2025 SM-102 Blade Replacement Installed new scraper QA Officer

    Annexure-2: Cleaning and Sanitization Log

    Date Machine ID Cleaning Agent Used Sanitization Method Verified By
    01/02/2025 SM-101 Sodium Hypochlorite Rinsed and Dried QA Head
    02/02/2025 SM-102 Ethyl Alcohol Wiped and Flushed 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 Handling Interruptions During Ointment Manufacturing - 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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