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 Operation of Sieving Machine

Posted on By

Standard Operating Procedure (SOP) for Operation of Sieving Machine

1. Purpose

The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the safe and efficient operation of the sieving machine in order to maintain the quality and integrity of pharmaceutical products.

2. Scope

This SOP applies to all personnel involved in operating the sieving machine within the pharmaceutical company.

3. Responsibilities

  • The Quality Assurance (QA) department is responsible for implementing and maintaining this SOP.
  • The Production department is responsible for operating the sieving machine.

4. Procedure

The following steps outline the procedure for the operation of the sieving machine:

See also  Tablet Manufacturing: SOP for Tablet Hardness Testing

4.1. Pre-Operation

  1. Inspect the sieving machine for any visible damage or malfunction.
  2. Ensure that all safety guards are in place and properly secured.
  3. Check the electrical connections and ensure they are properly grounded.
  4. Verify that the machine is clean and free from any residue or foreign particles.
  5. Check that the sieves are clean, in good condition, and properly installed in the machine.

4.2. Operation

  1. Switch on the power supply and ensure that the machine is properly connected.
  2. Set the desired sieving parameters (such as vibration intensity and duration) according to the product specifications.
  3. Ensure that the material to be sieved is prepared and placed in the feed hopper of the machine.
  4. Start the sieving process by
activating the machine.
  • Monitor the sieving operation to ensure smooth and consistent flow of material through the sieves.
  • Inspect the sieved material for any abnormalities or deviations from the required specifications.
  • If any issues or deviations are observed, immediately stop the machine and report them to the appropriate department for further investigation.
  • Once the sieving process is complete, switch off the machine and disconnect the power supply.
  • Clean the sieving machine thoroughly, including the sieves, to remove any residual material.
  • Properly store the sieving machine in its designated location.
  • 5. Abbreviations Used

    • QA: Quality Assurance
    • SOP: Standard Operating Procedure

    6. Documents

    • Sieving Machine Maintenance Log

    7. References

    No specific references are applicable for this SOP.

    8. SOP Version

    This is version 1.0 of the SOP for Operation of Sieving Machine.

     

    See also  SOP for Tablet Dedusting Process
    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: Microbiology Testing: SOP for Bioburden Testing
    Next Post: Quality Assurance: SOP for Water Testing

    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