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

Capsule Formulation: SOP for Weight Variation Control

Posted on By

Standard Operating Procedure for Weight Variation Control

Purpose

The purpose of this SOP is to establish procedures for controlling and monitoring weight variation in pharmaceutical products, ensuring compliance with regulatory standards and maintaining product quality.

Scope

This SOP applies to all personnel involved in the manufacturing and quality control of pharmaceutical products, specifically those responsible for weighing and dispensing operations.

Responsibilities

  • Operators: Responsible for accurately weighing and dispensing materials according to established procedures.
  • Quality Control Personnel: Responsible for monitoring and verifying weight variations in finished products.

Procedure

  1. Inspect weighing equipment for any visible damage or defects before each use.
  2. Ensure that weighing equipment is clean, calibrated, and meets the specifications for the intended use.
  3. Verify the accuracy of reference weights used in the calibration process.
  4. Calibrate weighing equipment regularly as per the approved calibration schedule.
  5. Perform linearity checks to ensure the accuracy of weighing equipment across the specified range.
  6. Use calibrated weighing equipment to dispense materials according to the approved batch record or formulation.
  7. Record the actual weights of materials dispensed and compare them with the target weights specified in the batch record.
  8. Calculate and document the percentage deviation from the target weight for each dispensed material.
  9. Ensure that the weight variation is within the acceptable limits defined in the relevant standard operating procedures or regulatory guidelines.
  10. Document any
out-of-specification (OOS) results and report them to the quality control department for investigation.
  • Implement corrective actions for identified deviations and prevent reoccurrence of weight variations.
  • Maintain accurate records of weight variation for each batch in the designated logbook or electronic system.
  • Review weight variation data periodically to identify trends or patterns that may require process adjustments.
  • Train personnel involved in weighing operations on proper procedures, equipment usage, and the importance of weight variation control.
  • Archive weight variation records in accordance with established retention policies.
  • Abbreviations

    No abbreviations are used in this SOP.

    Documents

    • Calibration Records
    • Weight Variation Logbook
    • Deviation and Corrective Action Logs

    Reference

    USP General Chapter <41> – Balances

    SOP Version

    Version 1.0

    See also  SOP for Raw Material Release
    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

    Post navigation

    Previous Post: Quality Assurance: SOP for Particle Size Analysis
    Next Post: Capsule Formulation, Quality Control: SOP for Content Uniformity 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