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Creams: SOP for Cleaning Homogenizers Post-Production – V 2.0

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Creams: SOP for Cleaning Homogenizers Post-Production – V 2.0

Standard Operating Procedure for Cleaning Homogenizers Post-Production

Department Creams
SOP No. SOP/CRM/086/2025
Supersedes SOP/CRM/086/2022
Page No. Page 1 of 5
Issue Date 21/01/2026
Effective Date 26/01/2026
Review Date 21/01/2027

1. Purpose

This SOP outlines the procedure for cleaning homogenizers post-production to ensure that they are free from residues and contaminants. The objective is to maintain hygienic conditions and prevent cross-contamination between batches.

2. Scope

This SOP applies to all homogenizers used in the Creams Department. It covers the cleaning process for homogenizers after each production run to ensure they are adequately sanitized before the next batch.

3. Responsibilities

  • Production Team: Responsible for following the SOP to clean the homogenizer after each production run, ensuring that all areas are cleaned thoroughly.
  • Maintenance Team: Ensures that the homogenizer is checked for wear and tear and performs any necessary repairs during the cleaning process.
  • Quality Control (QC): Ensures that the cleaning process meets the required standards and that there is no contamination of materials between batches.

4. Accountability

The Head of Production is accountable for ensuring that homogenizers are cleaned properly after each use. The QA Manager is responsible for verifying that the cleaning process complies with GMP standards and that the homogenizer is ready for use in the next production batch.

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5. Procedure

5.1 Pre-Cleaning Checks

  1. Ensure that the homogenizer has been turned off and disconnected from the power source before cleaning.
  2. Verify that all materials from the previous batch have been removed from the homogenizer, including any cream or emulsions.
  3. Ensure that all components to be cleaned (e.g., valves, nozzles, and hoses) are accessible and ready for cleaning.

5.2 Cleaning Process

  1. Rinse the homogenizer with warm water to remove any leftover product. Use a low-pressure flow to avoid splashing.
  2. Prepare a cleaning solution, usually a detergent solution compatible with food-grade or cosmetic production equipment. Follow the manufacturer’s recommendations for detergent concentration.
  3. Apply the cleaning solution to all parts of the homogenizer, including internal and external surfaces, seals, and nozzles. Use a clean, soft brush to scrub areas that may have accumulated product residue.
  4. Rinse the homogenizer thoroughly with warm water to remove all detergent residues.
  5. Sanitize the homogenizer with an appropriate sanitizing agent (e.g., alcohol-based sanitizer or other approved sanitizers). Follow the recommended contact time for the sanitizer to ensure effective disinfection.
  6. Rinse the homogenizer again with water to remove any residual sanitizer. Ensure that no cleaning or sanitizing agents remain in the system.

5.3 Post-Cleaning Inspection

  1. Inspect all components of the homogenizer, including the nozzles, hoses, and seals, to ensure they are thoroughly cleaned and free of residue.
  2. Ensure that there is no visible dirt or product residue on any part of the homogenizer.
  3. Check for any damage to the equipment that may have occurred during cleaning (e.g., broken seals or worn-out components). Document any repairs or replacements required in the Equipment Maintenance Log (Annexure-1).
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5.4 Drying the Homogenizer

  1. After cleaning and sanitizing, allow the homogenizer to air dry completely or use clean, dry compressed air to remove any remaining water from the internal components.
  2. Ensure that all components are completely dry before reassembling the homogenizer to prevent microbial growth or rusting.

5.5 Post-Cleaning Documentation

  1. Document the cleaning procedure in the Equipment Cleaning Log (Annexure-2), including the date, time, and operator details.
  2. Record any deviations from the standard cleaning procedure, including the reason for the deviation and any corrective actions taken.
  3. Document any maintenance performed during the cleaning process in the Equipment Maintenance Log (Annexure-1).

5.6 Reassembly and Readiness Check

  1. Reassemble the homogenizer and perform a readiness check to ensure that all components are securely attached and the machine is functioning correctly.
  2. Test the homogenizer with water or a non-product material to ensure it is operating properly before starting production with a new batch.

5.7 Final Approval

  1. The QA team must review the cleaning records to ensure that the homogenizer was cleaned in compliance with the SOP.
  2. Once approved, the homogenizer can be used for the next production run. If there are any issues or concerns, the batch production may be delayed until corrective actions are taken.
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6. Abbreviations

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

7. Documents

  1. Annexure-1: Equipment Maintenance Log
  2. Annexure-2: Equipment Cleaning Log

8. References

  • Good Manufacturing Practices (GMP) Guidelines – 21 CFR Part 211
  • International Conference on Harmonisation (ICH) Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
  • FDA Guidelines for Cosmetics Manufacturing

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

Equipment ID Maintenance Date Maintenance Type Operator Comments
HM-001 21/01/2026 Inspection, lubrication Jane Smith Successfully completed

Annexure-2: Equipment Cleaning Log

Equipment Cleaning Date Cleaning Method Operator Comments
Homogenizer 21/01/2026 Rinsed with warm water, detergent solution John Doe Cleaned after every batch

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/03/2024 1.0 Initial Version New SOP Creation QA Head
01/03/2025 2.0 Format Revision and Updates Standardization of Document QA Head
Creams V 2.0 Tags:Batch record documentation for creams, Change control procedures for cream manufacturing, Cleaning and sanitization SOPs in creams production, Complaint handling SOPs in creams production, Continuous improvement SOPs for cream manufacturing, Cream manufacturing process guidelines, Creams production documentation practices, Deviation handling SOPs in creams production, Employee training SOPs in creams manufacturing, Environmental monitoring SOPs in creams manufacturing, Equipment calibration SOPs for cream manufacturing, GMP compliance in creams production, Internal audit procedures in creams production, Packaging and labeling SOPs for creams, Pharmaceutical SOPs, Product quality review procedures for creams, Product release criteria SOPs for creams, Quality control SOPs for creams, ream manufacturing SOP, Regulatory requirements for cream production SOPs, Risk management SOPs in creams manufacturing, Stability testing SOPs for cream products, Standard operating procedures for skincare products, Supplier qualification SOPs for cream ingredients, Validation protocols for cream production processes

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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
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  • 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
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • 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
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  • Creams V 2.0
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