Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOP for Maintenance of Cleanroom Facilities

Posted on By




SOP for Maintenance of Cleanroom Facilities



Standard Operating Procedure for Maintenance of Cleanroom Facilities

1) Purpose

This SOP outlines the procedures for maintaining cleanroom facilities used in the production of nasal formulations. Cleanroom maintenance is critical for controlling contamination and maintaining air quality within the facility.

2) Scope

This SOP applies to all personnel responsible for maintaining the cleanliness, safety, and operational standards of cleanroom facilities at [Company Name].

3) Responsibilities

  • Cleanroom Operators: Responsible for cleaning and maintaining the cleanroom, including floors, walls, and equipment surfaces.
  • Quality Assurance (QA): Ensures that cleanroom environmental conditions, including air quality and surface cleanliness, meet the required specifications.
  • Maintenance Team: Responsible for maintaining HVAC systems, cleanroom integrity, and cleanliness monitoring systems.

4) Procedure

4.1 Daily Cleanroom Maintenance

4.1.1 Surface Cleaning

  • At the start of each shift, clean all surfaces, including floors, walls, and equipment surfaces, using an approved disinfectant solution. Follow a systematic cleaning pattern from the cleanest areas to the dirtiest.
  • Ensure that no dust, debris, or spilled liquids remain on any surface. Record the cleaning activities in the cleanroom cleaning log.
See also  SOP for Operating Lyophilizers for Nasal Powders

4.1.2 Equipment Cleaning

  • Disassemble any removable equipment parts, such as filters and
seals, and clean them with an approved cleaning agent. Rinse with sterile water and dry using lint-free wipes.
  • Inspect all cleaned equipment to ensure it is free from contamination and ready for use. Document the cleaning process in the equipment cleaning log.
  • 4.2 Weekly Cleanroom Maintenance

    4.2.1 Airflow and Pressure Testing

    • Test the air pressure differentials between the cleanroom and adjacent areas weekly. Verify that the airflow is laminar and that the cleanroom maintains the required positive pressure differential.
    • Record the results of airflow and pressure tests in the cleanroom environmental monitoring log. Notify the maintenance team if any deviations are detected.

    4.2.2 HEPA Filter Inspection

    • Inspect the HEPA filters in the HVAC system weekly for any blockages or signs of wear. Replace filters if the pressure differential exceeds acceptable limits or if filters appear damaged.
    • Document the filter inspection in the maintenance log and submit for QA review.

    4.3 Monthly Cleanroom Maintenance

    4.3.1 Deep Cleaning of Surfaces

    • Conduct a deep cleaning of all surfaces in the cleanroom at least once per month, using stronger disinfectant solutions. Pay special attention to hard-to-reach areas and clean beneath and behind equipment.
    • Ensure that all cleanroom fixtures, such as lighting and HVAC ducts, are cleaned thoroughly during deep cleaning. Record the deep cleaning in the cleanroom cleaning log.

    4.3.2 Monitoring Particle Counts

    • Measure particle counts in the cleanroom monthly using an approved particle counter. Compare the results with the specified limits for the cleanroom classification (e.g., ISO Class 5).
    • Document the particle count results in the environmental monitoring log and submit for QA approval.

    4.4 Annual Cleanroom Certification

    4.4.1 Full HVAC System Maintenance

    • Once per year, perform full maintenance on the cleanroom HVAC system, including duct cleaning, HEPA filter replacement, and recalibration of pressure control systems.
    • Document the HVAC system maintenance and submit the report for QA review.

    4.4.2 Cleanroom Recertification

    • Contract a certified cleanroom validation company annually to perform recertification of the cleanroom according to regulatory guidelines (e.g., ISO standards). Ensure that the cleanroom passes particle count, airflow, and microbial contamination tests.
    • Submit the cleanroom recertification report to QA for approval and archiving.

    5) Abbreviations, if any

    • HVAC: Heating, Ventilation, and Air Conditioning
    • QA: Quality Assurance

    6) Documents, if any

    • Cleanroom Cleaning Log
    • Equipment Cleaning Log
    • Environmental Monitoring Log
    • Maintenance Log

    7) References, if any

    • ISO 14644-1: Cleanrooms and associated controlled environments
    • Internal SOP for HVAC system maintenance

    8) SOP Version

    Version 1.0

    Annexure

    1. Cleanroom Cleaning Log Template

    Date Room ID Surface Cleaned Disinfectant Used Operator Initials QA Approval
    DD/MM/YYYY Room Identifier Surface Cleaned Disinfectant Name Operator Name QA Name
               


    See also  SOP for Formulating Nasal Sprays with Hydrophobic APIs
    Nasal Spray Formulations Tags:Cleaning SOP for nasal spray equipment, Environmental control in nasal spray production, Equipment maintenance for nasal sprays, Formulating isotonic nasal sprays, Microbial stability in nasal formulations, Mixing SOP for nasal formulations, Nasal spray API formulation, Nasal spray batch manufacturing SOP, Nasal spray filling machine operation, Nasal spray formulation process, Nasal spray GMP guidelines, Nasal spray homogenization techniques, Nasal spray manufacturing process, Nasal spray packaging SOP, Nasal spray preservative-free formulation, Nasal spray production SOP, Nasal spray stability studies, Nasal spray sterilization process, Nasal spray viscosity monitoring, Particle size control in nasal sprays, pH adjustment in nasal formulations, Quality control in nasal spray production, Solvent selection for nasal sprays, SOP for nasal spray manufacturing, SOP for nasal spray testing

    Post navigation

    Previous Post: SOP for Preparation of Emulsions for Oral Delivery
    Next Post: SOP for Preparation of Magnetic Nanoparticles for Biomedical Applications

    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

    Read SOPs in your Language:

     - 
    Bengali
     - 
    bn
    English
     - 
    en
    Gujarati
     - 
    gu
    Hindi
     - 
    hi
    Malayalam
     - 
    ml
    Marathi
     - 
    mr
    Punjabi
     - 
    pa
    Tamil
     - 
    ta
    Telugu
     - 
    te

    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.

    Copyright © 2025 SOP Guide for Pharma.

    Powered by PressBook WordPress theme

    Go to mobile version