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

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 HEPA Filter Integrity Testing

Posted on By

SOP for HEPA Filter Integrity Testing

Standard Operating Procedure for HEPA Filter Integrity Testing

1) Purpose

This SOP outlines the procedures for conducting HEPA filter integrity testing in cleanrooms or controlled environments.

2) Scope

This SOP applies to HEPA filter integrity testing conducted in cleanrooms or areas where high-efficiency particulate air (HEPA) filters are used for air filtration.

3) Responsibilities

The Facilities or Engineering department is responsible for performing HEPA filter integrity testing. Quality Assurance (QA) oversees the process and ensures compliance with this SOP and regulatory requirements.

4) Procedure

4.1 Preparation

  1. Review the HEPA filter integrity testing protocol and ensure all necessary materials and equipment are available (e.g., aerosol generator, photometer).
  2. Verify the calibration and functionality of the aerosol generator and photometer.
See also  SOP for Equipment Verification and Calibration

4.2 Testing Setup

  1. Prepare the cleanroom or controlled environment for testing by ensuring it is in the operational state.
  2. Isolate the area under test to prevent contamination during testing.

4.3 Testing Procedure

  1. Generate a specified aerosol challenge using the aerosol generator.
  2. Introduce the aerosol challenge upstream of the HEPA filter.
  3. Scan the downstream side of the HEPA filter with the photometer to measure aerosol penetration.
  4. Compare the photometer readings against acceptance criteria to determine filter integrity.
  5. Perform HEPA filter integrity testing in accordance with regulatory requirements and facility procedures.

4.4 Acceptance Criteria

  1. Ensure that the
HEPA filter passes the integrity test based on specified acceptance criteria for aerosol penetration.
  • Document any deviations from acceptance criteria and investigate root causes if necessary.
  • 4.5 Reporting and Documentation

    1. Document all testing activities, including results and any deviations, in the appropriate logbooks and records.
    2. Prepare a HEPA filter integrity testing report summarizing the findings for each test conducted.
    3. Review and approve the testing report to ensure accuracy and compliance with regulatory requirements.

    5) Abbreviations, if any

    SOP: Standard Operating Procedure
    HEPA: High-Efficiency Particulate Air
    QA: Quality Assurance

    6) Documents, if any

    HEPA Filter Integrity Testing Protocol, Testing Records, Testing Reports

    7) Reference, if any

    Regulatory guidelines such as ISO 14644-3:2019 Cleanrooms and associated controlled environments – Part 3: Test methods, European Pharmacopoeia (Ph. Eur.) 5.1.10 Guidance on the use of HEPA filters in clean rooms

    8) SOP Version

    Version 1.0

    See also  SOP for Annual Product Quality Review (APQR)
    Quality Assurance Tags:Batch Record Review SOP, CAPA SOP (Corrective and Preventive Actions), Change Control Management SOP, Cleaning Validation SOP, Documentation Control SOP, Equipment Qualification SOP, Finished Product Quality Assurance, Good Documentation Practices SOP, Handling Deviations SOP, In-process Quality Control SOP, Internal Quality Audits SOP, Out-of-Specification SOP, Packaging Material Quality Control, Pharmaceutical quality assurance SOP, Process Validation SOP, Product Complaint Handling SOP, Product Recall Management SOP, Quality Assurance Audits SOP, Quality Control Sample Management, Quality Risk Management SOP, Serialization and Traceability SOP, SOP for Raw Material Quality Assurance, Supplier Qualification SOP, Training and Competency Assessment SOP, Vendor Audits SOP

    Post navigation

    Previous Post: SOP for Risk Management in Procurement
    Next Post: SOP for Emergency Maintenance Procedures

    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