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SOP for Sifting and Sieving: Guidelines for Operating Sifters and Sieves, Including Particle Size Analysis and Documentation

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SOP for Sifting and Sieving: Guidelines for Operating Sifters and Sieves, Including Particle Size Analysis and Documentation

1) SOP for Operating Sifters and Sieves

2) Purpose

The purpose of this Standard Operating Procedure (SOP) is to provide detailed instructions for operating sifters and sieves, including guidelines for particle size analysis and documentation, to ensure consistent particle size distribution.

3) Scope

This SOP applies to all personnel involved in the operation of sifters and sieves within the pharmaceutical manufacturing area.

4) Responsibilities

  • Operators are responsible for setting up, operating, and cleaning sifters and sieves according to this SOP.
  • Supervisors are responsible for overseeing the sifting and sieving process and ensuring compliance.
  • Quality Assurance (QA) personnel are responsible for verifying that procedures are followed correctly and addressing any deviations.
See also  SOP for Raw Material Release

5) Procedure

  1. Preparation
    1. Ensure the sifting and sieving area is clean and free of contaminants.
    2. Verify the availability and quality of materials to be sifted or sieved as per the batch record.
    3. Check the cleanliness and readiness of the sifter and sieve equipment.
  2. Equipment Setup
    1. Select the appropriate sieve mesh size based on the product specifications.
    2. Assemble the sifter and sieve according to the manufacturer’s instructions.
    3. Ensure that all components are securely in place and properly aligned.
    4. Set the machine parameters (e.g., vibration intensity, duration) according to the batch record.
  3. Sifting and Sieving Process
    1. Load the materials into the sifter or sieve.
    2. Start the machine and monitor the sifting or sieving process continuously.
    3. Ensure that the particle size distribution meets the specified criteria by sampling and testing the output at regular intervals.
    4. Adjust the machine settings if necessary to maintain consistency.
    5. Document any observations and adjustments made during the sifting or sieving process.
  4. Troubleshooting
    1. If the machine malfunctions, stop the operation immediately and troubleshoot the issue.
    2. Refer to the manufacturer’s manual for troubleshooting guidelines.
    3. Document the issue and the corrective actions taken in the maintenance logbook.
    4. Resume operation once the issue is resolved and the machine is functioning properly.
  5. Cleaning and Maintenance
    1. Turn off and disassemble the sifter or sieve according to the manufacturer’s instructions.
    2. Clean all parts thoroughly to prevent cross-contamination.
    3. Document the cleaning process in the cleaning logbook.
    4. Perform regular maintenance checks and document them in the maintenance logbook.
See also  Capsule Formulation: SOP for Content Uniformity Testing

6) Abbreviations, if any

  • SOP: Standard Operating Procedure
  • QA: Quality Assurance

7) Documents, if any

  • Batch Record
  • Cleaning Logbook
  • Maintenance Logbook

8) Reference, if any

  • Current Good Manufacturing Practice (cGMP) guidelines
  • Manufacturer’s operation and maintenance manual

9) SOP Version

Version 1.0

Capsule Formulation 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

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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

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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

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