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SOP for Capsule Inspection

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Standard Operating Procedure for Capsule Inspection

Purpose

The purpose of this SOP is to establish procedures for the visual inspection and quality control of capsules, ensuring adherence to quality standards, and the identification of defects or deviations.

Scope

This SOP applies to all personnel involved in the capsule inspection process, including inspectors, quality control personnel, and supervisors.

Responsibilities

  • Inspectors: Responsible for visually inspecting capsules according to the established procedures.
  • Quality Control Personnel: Responsible for monitoring and ensuring compliance with the capsule inspection SOP.
  • Supervisors: Responsible for overseeing the capsule inspection process and providing necessary support to inspectors.
See also  SOP for Handling of Deviations and Incidents: Procedures for Identifying, Documenting, and Investigating Deviations, Incidents, or Non-conformances in the Manufacturing Process

Procedure

  1. Ensure that the capsule inspection area is clean, well-lit, and free from any potential contaminants.
  2. Verify that the inspection equipment, such as magnifying glasses or automated inspection machines, is calibrated and functioning correctly.
  3. Inspect the capsules visually for any defects, including but not limited to cracks, discoloration, and irregularities in size or shape.
  4. Set up any necessary magnification equipment to aid in the detailed inspection of capsules.
  5. Sort the inspected capsules into accepted and rejected categories based on the predefined acceptance criteria.
  6. If using automated inspection machines, ensure that the equipment is programmed with the correct inspection parameters.
  7. Perform periodic checks on the automated inspection machine to ensure accurate and consistent results.
  8. If defects are identified, document the type
and number of defects found, and initiate the appropriate corrective actions.
  • Record the inspection results, including the number of accepted and rejected capsules, in the inspection log or batch record.
  • Submit rejected capsules to the quality control laboratory for further analysis if required.
  • If adjustments to the inspection process are necessary, document the changes made and the reason for the adjustments.
  • Report any trends or recurring issues in capsule defects to the quality control department for investigation and resolution.
  • Complete the logbook or batch record with all pertinent information, including any adjustments made during the capsule inspection process.
  • Clean and sanitize the inspection area and equipment regularly according to the approved cleaning procedures.
  • Abbreviations

    No abbreviations are used in this SOP.

    Documents

    • Capsule Inspection Logbook
    • Quality Control Test Results
    • Deviation and Corrective Action Logs

    Reference

    USP General Chapter <797> – Pharmaceutical Compounding – Sterile Preparations

    SOP Version

    Version 1.0

    See also  SOP for Particle Size Analysis: Guidelines for Conducting Particle Size Analysis Using Particle Size Analysers and Interpreting the Results
    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
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    • Lotions
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    • Nanoparticle Formulation
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    • Pharmacovigilance
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    • 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

    New Publication: A must for All.

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