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

Quality Assurance: SOP for Particle Size Analysis

Posted on By

Standard Operating Procedure for Particle Size Analysis

Purpose

The purpose of this SOP is to establish procedures for the accurate and consistent analysis of particle size in pharmaceutical products, ensuring compliance with regulatory standards and product quality.

Scope

This SOP applies to all personnel involved in particle size analysis, including laboratory technicians and quality control personnel.

Responsibilities

  • Laboratory Technicians: Responsible for conducting particle size analysis following established procedures.
  • Quality Control Personnel: Responsible for reviewing and approving particle size analysis results for compliance.

Procedure

  1. Inspect the particle size analysis equipment for any visible damage or defects before each use.
  2. Ensure that the equipment is clean, calibrated, and properly set up for the specific particle size analysis method to be employed.
  3. Prepare the sample to be analyzed according to the approved sampling plan, ensuring representative and homogenous samples.
  4. Load the sample into the particle size analysis equipment, following the instrument-specific loading procedure.
  5. Run the particle size analysis according to the established method, specifying parameters such as dispersion medium and analysis time.
  6. Monitor the instrument during the analysis process, addressing any issues or deviations promptly.
  7. Record the particle size analysis results, including size distribution and any other relevant data, in the designated logbook or electronic system.
  8. If adjustments to the analysis parameters are necessary, document the changes made and the
reason for the adjustments.
  • Perform routine checks and calibrations of the particle size analysis equipment to ensure accurate and reliable results.
  • Perform validation checks if required for the specific particle size analysis method being used.
  • Review the particle size analysis results for compliance with predefined specifications and acceptance criteria.
  • Document any out-of-specification (OOS) results, initiate an investigation, and implement corrective actions as needed.
  • Archive particle size analysis records in accordance with established retention policies.
  • Regularly review and update the particle size analysis method as needed based on industry standards or process changes.
  • Abbreviations

    No abbreviations are used in this SOP.

    Documents

    • Particle Size Analysis Logbook
    • Calibration Records
    • Validation Reports
    • Deviation and Corrective Action Logs

    Reference

    USP General Chapter <429> – Design and Development of Bioanalytical Methods

    SOP Version

    Version 1.0

    See also  SOP for Laboratory Instrument Maintenance
    Quality Assurance Tags:Capsule Batch Record, Capsule Blending, Capsule Cleaning Validation, Capsule Coating, Capsule Deviation Investigation, Capsule Dosage Form, Capsule Encapsulation, Capsule Equipment Qualification, Capsule Filling, Capsule Formulation SOP, Capsule Inspection Procedure, Capsule Integrity, Capsule Manufacturing, Capsule Mixing, Capsule Polishing, Capsule Production, Capsule Quality Control, Capsule Sampling, Capsule Shell Inspection, Capsule Weight Check

    Post navigation

    Previous Post: SOP for Bulk Powder Handling
    Next Post: Capsule Formulation: SOP for Weight Variation Control

    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