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Elixir Department: SOP for Cleaning of Inline Filters and Screens – V 2.0

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Elixir Department: SOP for Cleaning of Inline Filters and Screens – V 2.0

Standard Operating Procedure for Cleaning of Inline Filters and Screens in Elixir Manufacturing

Department Elixir Department
SOP No. SOP/ELX/163/2025
Supersedes SOP/ELX/163/2022
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 standard procedure for disassembly, cleaning, inspection, and reassembly of inline filters and mesh screens used in elixir manufacturing processes to ensure product quality and compliance with cGMP standards.

2. Scope

This SOP applies to all inline filters, strainers, and mesh screens connected to pipelines, filling lines, holding tanks, and transfer units in the Elixir Department.

3. Responsibilities

  • Production Operator:
    • Disassemble, clean, and inspect inline filters/screens post-batch.
    • Document the activity in the cleaning logbook.
  • Engineering Department:
    • Support complex filter housing disassembly and maintenance of seals and clamps.
  • QA Officer:
    • Verify cleaning effectiveness and authorize reuse or storage of filters/screens.
See also  Elixir Department: SOP for Digital Weighing Balance Usage - V 2.0

4. Accountability

The Production Head is accountable for timely cleaning post each batch. The Engineering Head ensures system operability and integrity. QA Head ensures compliance and approval before reuse.

5. Procedure

5.1 Disassembly

  1. Ensure product transfer is complete and line is emptied.
  2. Switch off equipment and label as “Under Maintenance.”
  3. Wear PPE including gloves, face mask, apron, and safety goggles.
  4. Loosen clamp bolts or screw fittings to open the filter housing.
  5. Remove mesh screen or cartridge filter carefully without bending or damaging.

5.2 Cleaning

  1. Rinse filters/screens under running purified water to remove loose particles.
  2. Immerse in 1% non-ionic detergent solution and brush gently with a nylon brush.
  3. Pay special attention to mesh corners, crevices, and filter surface.
  4. Rinse thoroughly with purified water until no foam or residue remains.
  5. If applicable, perform final rinse using hot purified water (60–80°C).
See also  Elixir Department: SOP for Use of Water for Injection (WFI) in Elixir Production - V 2.0

5.3 Drying and Inspection

  1. Dry the filter/screen using compressed air filtered through 0.22 µm filter or place in drying cabinet.
  2. Inspect visually for:
    • Clogging
    • Tears or mesh distortion
    • Corrosion or rust marks
  3. If any damage is observed, report to Engineering and replace the filter.

5.4 Reassembly

  1. Reassemble the filter into the housing using proper orientation.
  2. Ensure gaskets or O-rings are intact and properly seated.
  3. Tighten clamps or screws using torque wrench if specified.

5.5 Documentation and Release

  1. Record the cleaning activity in the Inline Filter Cleaning Logbook (Annexure-1).
  2. QA to verify filter condition and cleanliness.
  3. Label as “CLEANED” and approve for next use.

6. Abbreviations

  • SOP: Standard Operating Procedure
  • QA: Quality Assurance
  • PPE: Personal Protective Equipment
  • CIP: Clean-In-Place

See also  Elixir Department: SOP for Use of Material Transfer Hatches - V 2.0

7. Documents

  1. Inline Filter Cleaning Logbook (Annexure-1)
  2. Filter Inspection Checklist
  3. Swab/Rinse Test Reports (if applicable)

8. References

  • 21 CFR Part 211.67 – Cleaning of Equipment
  • WHO TRS 986 Annex 2 – Good Manufacturing Practices
  • ICH Q9 – Quality Risk Management

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Inline Filter Cleaning Logbook

Date Filter ID Equipment Name Cleaned By QA Verified Remarks
11/04/2025 FILT-ELX-03 Filling Line 2 Rajesh Kumar Sunita Reddy No damage, Cleaned

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/01/2024 1.0 Initial SOP Release New Procedure Documentation QA Head
11/04/2025 2.0 Added hot water rinse and filter damage inspection Enhanced Compliance QA Head
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
  • Tablet Manufacturing V2.0

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