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Elixir Department: SOP for Visual Inspection Post Cleaning – V 2.0

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Elixir Department: SOP for Visual Inspection Post Cleaning – V 2.0

Standard Operating Procedure for Visual Inspection Post Cleaning in Elixir Manufacturing

Department Elixir Department
SOP No. SOP/ELX/171/2025
Supersedes SOP/ELX/171/2022
Page No. Page 1 of 10
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To define the procedure for conducting visual inspection of equipment, utensils, and product-contact surfaces after cleaning, ensuring removal of visible residues and suitability for next use in elixir manufacturing.

2. Scope

This SOP applies to all cleaned and rinsed equipment, tanks, pipelines, filling machines, accessories, and utensils within the Elixir Department that require visual verification before use or further testing.

3. Responsibilities

  • Production Operator:
    • Perform preliminary visual inspection and report any non-conformities.
  • QA Officer:
    • Carry out formal visual inspection under suitable lighting conditions.
    • Approve or reject equipment for further processing.
See also  Elixir Department: SOP for Detergent Solution Preparation for Cleaning - V 2.0

4. Accountability

The Production Head is accountable for ensuring that visual inspection is conducted post-cleaning. The QA Head ensures documented verification and compliance with acceptance criteria.

5. Procedure

5.1 Preparation for Inspection

  1. Ensure that the cleaning process has been completed
and documented.
  • Verify that rinse water meets pH, conductivity, and TOC requirements (if applicable).
  • Ensure adequate lighting is available for internal and external surface examination (minimum 540 lux for open areas and 1080 lux for interior inspection).
  • 5.2 Visual Inspection Process

    1. Inspect all product-contact surfaces for the presence of:
      • Residues (powder, liquids, color stains, sticky mass)
      • Fibers or lint from cleaning cloths
      • Water droplets or standing water
      • Corrosion, cracks, dents, or discoloration
    2. Inspect critical areas such as:
      • Bottom valves, nozzles, manways
      • Gasket grooves and crevices
      • Joints and connections
    3. Use inspection mirrors and flashlights where required for internal surfaces.
    4. If any residue is observed, inform the Production Head and initiate re-cleaning before reinspection.

    5.3 Documentation

    1. Record inspection findings in the Visual Inspection Logbook (Annexure-1).
    2. Include details such as date, equipment ID, type of inspection, performed by, observations, and QA decision.
    3. Label equipment as “VISUALLY CLEANED – APPROVED” or “REJECTED – TO BE RE-CLEANED.”

    6. Abbreviations

    • SOP: Standard Operating Procedure
    • QA: Quality Assurance
    • TOC: Total Organic Carbon

    7. Documents

    1. Visual Inspection Logbook (Annexure-1)
    2. Cleaning Record Sheet
    3. QA Verification Checklist

    8. References

    • 21 CFR Part 211.67 – Equipment Cleaning and Maintenance
    • ICH Q7 – GMP Guidelines for APIs
    • WHO TRS 986 Annex 4 – Cleaning Validation

    9. SOP Version

    Version: 2.0

    10. Approval Section

    Prepared By Checked By Approved By
    Signature
    Date
    Name
    Designation
    Department

    11. Annexures

    Annexure-1: Visual Inspection Logbook

    Date Equipment ID Type of Inspection Inspected By QA Verified Status Remarks
    11/04/2025 MXR-ELX-12 Post-Cleaning Rajesh Kumar Sunita Reddy Approved Visually Clean

    Revision History:

    Revision Date Revision No. Revision Details Reason for Revision Approved By
    01/01/2024 1.0 Initial Release New SOP QA Head
    11/04/2025 2.0 Included lux requirement and critical point checklist Audit Enhancement QA Head
    See also  Elixir Department: SOP for Sampling from Storage Tank - V 2.0
    Elixers V 2.0 Tags:Elixir colorants, Elixir dosage form, Elixir filtration techniques, Elixir flavoring agents, Elixir formulation, Elixir GMP compliance, Elixir manufacturing process, Elixir manufacturing SOPs, Elixir packaging requirements, Elixir pharmacopoeial standards, Elixir preparation methods, Elixir preservatives, Elixir production equipment, Elixir quality control, Elixir regulatory guidelines, Elixir shelf life, Elixir stability testing, Elixir sterilization methods, Elixir storage conditions, Elixir sweetening agents, Elixir viscosity modifiers, Hydroalcoholic solutions, Medicated elixirs, Non-medicated elixirs, Pharmaceutical elixirs

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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
    • Gels V 2.0
    • Injectables V 2.0
    • Ointments V 2.0
    • Raw Material Warehouse V 2.0
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