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
  • SOP Guidelines
    • SOP Development
    • SOP Training
    • SOP Compliance Monitoring
    • SOP Revision Processes
    • Pharmaceutical SOP templates
    • GMP documentation SOP
    • Data integrity SOP pharma
    • Manufacturing SOP pharmaceutical
    • FDA SOP guidance
    • eQMS SOP workflows
  • 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)
  • GMP Audit Findings
    • Non-Compliance
      • SOP Absence
      • Revision Control
      • Non-Adherence
      • Poor Writing
      • Training Failure
      • Data Integrity Gaps
      • Mismatch Between SOPs and Practice
      • Critical Operations
      • Regulatory Change
      • Emergency Changes
      • Third-Party SOPs
      • Inspection Readiness
      • Deviation Handling
      • CAPA Integration
      • Validation Alignment
      • System Integration
      • Uncontrolled Distribution
      • SOP Implementation Gaps
      • SOP Alignment with Validation
      • Change Control Linkage
  • Toggle search form

Elixir Department: SOP for Weekly Preventive Cleaning – V 2.0

Posted on By

Elixir Department: SOP for Weekly Preventive Cleaning – V 2.0

Standard Operating Procedure for Weekly Preventive Cleaning in Elixir Manufacturing

Department Elixir Department
SOP No. SOP/ELX/181/2025
Supersedes SOP/ELX/181/2022
Page No. Page 1 of 9
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To establish a standard procedure for performing weekly preventive cleaning of manufacturing equipment, accessories, and working areas in the Elixir Department to prevent accumulation of residues and ensure a state of readiness.

2. Scope

This SOP applies to all product-contact and non-contact equipment surfaces, external areas of processing tanks, floors, walls, utilities, and fixtures in the Elixir manufacturing area that require preventive cleaning at weekly intervals.

3. Responsibilities

  • Production Operator:
    • Perform cleaning activities as per schedule.
    • Ensure proper documentation of cleaning activity.
  • Production Supervisor:
    • Verify the completion of preventive cleaning and sign off the checklist.
  • QA Officer:
    • Perform random verification and review cleaning records weekly.
See also  Elixir Department: SOP for Sampling of Final Product for QC - V 2.0

4. Accountability

The Production Head is accountable for ensuring compliance with the preventive cleaning schedule. QA is responsible for reviewing records and ensuring the cleaning effectiveness.

5. Procedure

5.1

Schedule and Planning
  1. Prepare a weekly cleaning calendar for each processing area, listing equipment, location, and responsible personnel.
  2. Display the calendar in the production area and update with completion status every week.

5.2 Materials Required

  • Approved cleaning detergent (1–2% solution)
  • Lint-free cloths and scrubbers
  • Sanitizer (e.g., 70% IPA)
  • Approved brushes and mops
  • Buckets labeled for detergent and rinse water

5.3 Cleaning Steps

  1. Switch off equipment and disconnect from utilities before cleaning.
  2. Perform the following cleaning tasks:
    • Wipe down external surfaces of tanks, vessels, and pipelines.
    • Clean handles, clamps, and equipment support stands.
    • Sweep and mop floors with detergent followed by water rinse.
    • Wipe wall panels, light fixtures, and glass view panels.
    • Sanitize contact surfaces using 70% IPA after drying.
  3. Inspect cleaned areas and note any issues (e.g., corrosion, residue).
  4. Escalate observations requiring maintenance or deep cleaning.

5.4 Frequency and Exceptions

  1. Perform preventive cleaning once every 7 days.
  2. If production schedule does not allow cleaning on the 7th day, extend up to 9th day with QA approval and justification.
  3. Document reasons for delay in the cleaning calendar and get countersigned by Production Head and QA.

5.5 Documentation

  1. Record each weekly cleaning activity in the Preventive Cleaning Logbook (Annexure-1).
  2. Supervisor to verify and sign upon completion.
  3. QA to review weekly and maintain cleaning compliance summary.

6. Abbreviations

  • SOP: Standard Operating Procedure
  • QA: Quality Assurance
  • IPA: Isopropyl Alcohol

7. Documents

  1. Preventive Cleaning Logbook (Annexure-1)
  2. Weekly Cleaning Calendar

8. References

  • 21 CFR Part 211.67 – Cleaning and Maintenance
  • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
  • WHO TRS 986 Annex 4 – Pharmaceutical Cleaning Guidelines

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Preventive Cleaning Logbook

Date Equipment/Area Cleaning Agent Cleaned By Verified By Remarks
11/04/2025 Tank Exterior – MXR-ELX-07 1% Neutraclean Rajesh Kumar Sunita Reddy Completed – No Observations

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 weekly calendar and delay protocol Audit Recommendation 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

Post navigation

Previous Post: Biosimilars: SOP for Precipitation and Clarification Steps – V 2.0
Next Post: Manufacturing: SOP for Ensuring Compliance with Critical Process Parameters – V 2.0

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
  • Gels V 2.0
  • Injectables 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