Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • 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)
  • SOP – Blog Post
  • Toggle search form

Ointments: SOP for Cleaning Heating Jacketed Vessels – V 2.0

Posted on By

SOP for Cleaning Heating Jacketed Vessels – V 2.0

Procedure for Cleaning Heating Jacketed Vessels

Department Production/Engineering/Quality Assurance (QA)
SOP No. SOP/Ointment/055
Supersedes V 1.0
Page No. Page X of Y
Issue Date [Insert Issue Date]
Effective Date [Insert Effective Date]
Review Date [Insert Review Date]

1. Purpose

The purpose of this Standard Operating Procedure (SOP) is to establish a standardized method for cleaning heating jacketed vessels used in ointment manufacturing. Proper cleaning ensures the removal of residues, prevents contamination, and maintains compliance with Good Manufacturing Practices (GMP).

2. Scope

This SOP applies to all personnel involved in the cleaning and maintenance of heating jacketed vessels used in the production of ointments.

3. Responsibilities

  • Production Supervisor: Ensures cleaning activities are performed as per SOP guidelines.
  • Machine Operator: Prepares the vessel for cleaning and performs initial rinsing.
  • Cleaning Personnel: Conducts thorough cleaning and sanitization of the vessel.
  • Quality Assurance (QA) Personnel: Inspects and verifies the cleaning effectiveness.
  • Engineering Technician: Assists in troubleshooting mechanical issues related to the heating jacket.
See also  Ointments: SOP for Operating Cooling Tunnels - V 2.0

4. Accountability

The Production, Engineering, and QA Managers are accountable for ensuring that heating jacketed vessel cleaning follows GMP standards and is properly documented.

5. Procedure

5.1 Pre-Cleaning Preparations

  • Ensure the vessel is empty and disconnected from power and steam supply.
  • Depressurize the heating jacket system to avoid hazards.
  • Wear appropriate Personal Protective Equipment (PPE), including gloves, goggles, and aprons.
  • Ensure that all necessary cleaning
materials and equipment are available.

5.2 Initial Rinsing

  • Flush the interior of the vessel with purified water to remove loose residues.
  • Drain completely before proceeding to detergent cleaning.

5.3 Cleaning Process

5.3.1 Detergent Cleaning

  • Prepare a cleaning solution using an approved detergent.
  • Circulate the cleaning solution in the vessel for at least 15 minutes.
  • Use soft brushes or scrubbing pads to clean the interior surfaces, including the walls and base.
  • Ensure that the heating jacket’s external surface is also cleaned.

5.3.2 High-Pressure Rinsing

  • Use high-pressure purified water to rinse off detergent residues.
  • Ensure complete removal of any detergent traces.

5.3.3 Final Sanitization

  • Apply an approved sanitizing agent (e.g., 70% ethanol or peracetic acid solution).
  • Allow sufficient contact time (10-15 minutes) for effective disinfection.
  • Perform a final rinse with purified water.

5.4 Cleaning the Heating Jacket

  • Flush the heating jacket with an appropriate descaling agent if mineral buildup is detected.
  • Rinse with purified water to remove any descaling agent residues.
  • Ensure all drainage points are clear and free from blockages.

5.5 Drying and Post-Cleaning Inspection

  • Allow the vessel to air dry completely in a controlled environment.
  • Conduct a visual inspection to ensure no residues remain.
  • Perform swab tests to verify microbial cleanliness.
  • Record the results in the Cleaning Log.

5.6 Documentation and Approval

  • Log all cleaning activities in the Cleaning Record.
  • QA personnel must review and approve the cleaning before the next batch.
  • Store records for compliance audits.

6. Abbreviations

  • GMP – Good Manufacturing Practices
  • QA – Quality Assurance
  • QC – Quality Control
  • PPE – Personal Protective Equipment

7. Documents

  • Cleaning Log (Annexure-1)
  • Cleaning Validation Report (Annexure-2)

8. References

  • WHO GMP Guidelines for Pharmaceutical Manufacturing
  • 21 CFR Part 211 – Current Good Manufacturing Practices
  • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients

9. SOP Version

Version 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Cleaning Log

Date Vessel ID Cleaning Solution Used Sanitization Agent Verified By
01/02/2025 HJ-101 Detergent Solution 70% Ethanol QA Officer
02/02/2025 HJ-102 Alkaline Cleaner Peracetic Acid QA Officer

Annexure-2: Cleaning Validation Report

Date Vessel ID Swab Test Result Microbial Limits Final Status Approved By
01/02/2025 HJ-101 Pass Within Limit Approved QA Head
02/02/2025 HJ-102 Pass Within Limit Approved QA Head

12. Revision History:

Revision Date Revision No. Details of Revision Reason for Revision Approved By
01/01/2024 1.0 Initial Version New SOP QA Head
01/02/2025 2.0 Updated SOP Format Standardization of Document QA Head
See also  Ointments: SOP for Evaluating Sensory Attributes of Ointments - V 2.0
Ointments V 2.0 Tags:Ointment application SOP, Ointment batch record SOP, Ointment compounding SOP, Ointment dispensing SOP, Ointment filling SOP, Ointment formulation SOP, Ointment manufacturing SOP, Ointment microbiological testing SOP, Ointment pH testing SOP, Ointment production SOP, Ointment quality control SOP, Ointment stability study SOP, Pharmaceutical ointment SOP, SOP for ointment homogenization, SOP for ointment labeling, SOP for ointment mixing, SOP for ointment packaging, SOP for ointment preparation, SOP for ointment raw material testing, SOP for ointment shelf-life determination, SOP for ointment stability testing, SOP for ointment sterilization, SOP for ointment storage, SOP for ointment testing, SOP for ointment viscosity testing

Post navigation

Previous Post: Tablets: SOP for API Uniformity in Tablet Granules – V 2.0
Next Post: SOP for Screening Formulations for Injectable Delivery

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
  • 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