SOP Guide for Pharma

Elixir Department: SOP for Cleaning and Sanitization of Storage Vessels – V 2.0

Elixir Department: SOP for Cleaning and Sanitization of Storage Vessels – V 2.0

Standard Operating Procedure for Cleaning and Sanitization of Storage Vessels in Elixir Manufacturing

Department Elixir Department
SOP No. SOP/ELX/082/2025
Supersedes SOP/ELX/082/2022
Page No. Page 1 of 8
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To establish a validated procedure for the cleaning and sanitization of storage vessels used in the Elixir Department to ensure removal of product residues, prevent cross-contamination, and maintain microbial control.

2. Scope

This SOP applies to all portable and fixed stainless-steel storage vessels used to hold intermediate or final bulk elixir formulations prior to filtration or packaging.

3. Responsibilities

  • Production Operator:
    • Perform cleaning and sanitization as per procedure and document all activities.
  • Production Supervisor:
    • Verify vessel cleaning status and ensure tagging is correctly updated.
  • QA Officer:
    • Review cleaning log and visually inspect vessel prior to next use.

4. Accountability

The Head of Production is accountable for ensuring that all storage vessels are cleaned and sanitized according to this SOP and that records are complete and accurate.

5. Procedure

5.1 Cleaning Frequency

  1. Clean the storage vessel:
    • Immediately after batch transfer/use
    • Before use if not used within 72 hours of last cleaning
    • After any suspected contamination event

5.2 Cleaning Procedure

  1. Ensure the vessel is disconnected from all inlet/outlet hoses and emptied completely.
  2. Rinse vessel with potable water to remove gross residues.
  3. Scrub interior surfaces using soft-bristle brush with 2% non-ionic detergent solution.
  4. Rinse thoroughly with potable water followed by purified water until rinse water is clear.
  5. Visually inspect for any remaining residue. Repeat cleaning if needed.

5.3 Sanitization Procedure

  1. Prepare 0.1% v/v sodium hypochlorite solution or any approved sanitizing agent.
  2. Circulate or spray the solution throughout the vessel for 10–15 minutes ensuring full surface contact.
  3. Drain and rinse the vessel with Water for Injection (WFI) to remove sanitizer residue.
  4. Allow vessel to air dry in a clean area or wipe with sterile lint-free cloth if required.

5.4 Post-Cleaning Activities

  1. Label the cleaned vessel with a “CLEANED” status tag (Annexure-1).
  2. Record cleaning and sanitization details in the Cleaning Logbook (Annexure-2).
  3. Ensure cleaning validation data is attached, where applicable.

5.5 Precautions

  1. Use dedicated scrubbers and accessories per vessel.
  2. Use protective gloves and goggles during chemical handling.
  3. Never mix cleaning agents or sanitizers unless validated for compatibility.

6. Abbreviations

  • SOP: Standard Operating Procedure
  • WFI: Water for Injection
  • QA: Quality Assurance

7. Documents

  1. Cleaned Vessel Tag (Annexure-1)
  2. Cleaning Logbook (Annexure-2)
  3. Cleaning Validation Report (where applicable)

8. References

  • 21 CFR Part 211.67 – Equipment Cleaning and Maintenance
  • WHO TRS 986 – GMP for Pharmaceuticals

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Cleaned Vessel Tag

Tank ID Product Last Processed Cleaned By Cleaning Date Status
ST-02 Paracetamol Elixir Rajesh Kumar 11/04/2025 CLEANED

Annexure-2: Cleaning Logbook

Date Tank ID Batch No. Cleaned By Sanitized By QA Verified Remarks
11/04/2025 ST-02 ELX-1021 Rajesh Kumar Sunita Reddy Yes Approved for reuse

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/01/2024 1.0 Initial SOP Release New SOP QA Head
11/04/2025 2.0 Added sanitization steps and validation reference GMP Compliance QA Head
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