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 Handling and Maintenance of Friability Testing Equipment

Posted on By

Standard Operating Procedure for Handling and Maintenance of Friability Testing Equipment

Purpose

The purpose of this SOP is to provide comprehensive guidelines for the proper handling and maintenance of friability testing equipment in pharmaceutical manufacturing. Proper handling and regular maintenance of the equipment are essential to ensure accurate and reliable friability test results, contributing to the assessment of tablet quality and compliance with regulatory standards. By following this SOP, we can ensure the equipment’s longevity and optimal performance, ultimately leading to superior product quality.

Scope

This SOP applies to all personnel involved in the handling and maintenance of friability testing equipment within the pharmaceutical company.

See also  SOP for Tablet Dedusting Process

Responsibilities

  • The Quality Assurance (QA) department is responsible for implementing and maintaining this SOP.
  • The Production department is responsible for the proper handling and maintenance of friability testing equipment.

Procedure

Handling of Friability Testing Equipment

  • Handle friability testing equipment with care and avoid any rough or careless handling that may cause damage.
  • Use the equipment only for its intended purpose, which is conducting friability tests on tablets or other solid dosage forms.
  • Always wear appropriate personal protective equipment (PPE), such as gloves and safety glasses, when operating the equipment.
  • Ensure that the working area is clean and free from any dust or contaminants that may affect
the accuracy of the friability tests.
  • Follow the manufacturer’s instructions and guidelines for the proper use of the friability testing equipment.
  • Maintenance of Friability Testing Equipment

    • Perform regular maintenance checks on the friability testing equipment as per the manufacturer’s recommendations and schedule.
    • Inspect the equipment for any signs of wear, damage, or malfunction, and take immediate corrective action if necessary.
    • Clean the equipment regularly, both externally and internally, using appropriate cleaning agents and tools.
    • Keep the testing area clean and organized, and store the equipment properly when not in use.
    • Keep a record of all maintenance activities, including dates, maintenance performed, and any parts replaced.

    Calibration of Friability Testing Equipment

    • Calibrate the friability testing equipment as per the manufacturer’s instructions and recommended frequency.
    • Use certified calibration standards and reference materials for accurate calibration.
    • Record all calibration details, including dates, calibration standards used, and results obtained.
    • Take corrective actions if any deviations are observed during the calibration process.

    Abbreviations

    • QA: Quality Assurance
    • SOP: Standard Operating Procedure
    • PPE: Personal Protective Equipment

    Documents

    • Friability Testing Equipment Maintenance Log
    • Friability Testing Equipment Calibration Log

    References

    No specific references are applicable for this SOP.

    SOP Version

    This is version 1.0 of the SOP for Handling and Maintenance of Friability Testing Equipment.

     

    See also  SOP for Operation of Hot Water Bath
    Quality Control, Tablet Manufacturing Tags:Tablet batch record review, Tablet blending SOP, Tablet cleaning and maintenance, Tablet coating procedure, Tablet compression SOP, Tablet disintegration test procedure, Tablet dissolution procedure, Tablet formulation SOP, Tablet friability testing SOP, Tablet labeling and packaging SOP, Tablet manufacturing equipment SOP, Tablet manufacturing SOP, Tablet packaging SOP, Tablet production procedure, Tablet quality control SOP, Tablet sampling and in-process testing SOP, Tablet stability testing SOP, Tablet storage and handling procedure, Tablet uniformity testing procedure, Tablet weight variation SOP

    Post navigation

    Previous Post: SOP for Calibration and Verification of Friability Tester
    Next Post: SOP for Operation of Tablet Disintegration Tester

    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