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

SOP for Sterilization Tunnel

Posted on By

SOP for Sterilization Tunnel

Standard Operating Procedure for Using Sterilization Tunnel

1) Purpose

The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the sterilization tunnel used in the manufacturing of otic dosage forms to ensure effective sterilization of containers and closures.

2) Scope

This SOP applies to all personnel involved in the operation and maintenance of the sterilization tunnel in the pharmaceutical manufacturing facility.

3) Responsibilities

Operators: Responsible for correctly operating the sterilization tunnel as per this SOP.
Quality Control (QC) Personnel: Responsible for monitoring the sterilization process and verifying results.
Maintenance Personnel: Responsible for maintaining the sterilization tunnel in proper working condition.

See also  SOP for Manufacturing Process Control

4) Procedure

4.1 Operation
4.1.1 Preparation
4.1.1.1 Ensure the sterilization tunnel is on a stable, level surface.
4.1.1.2 Check that the tunnel is clean and free of any debris.
4.1.1.3 Verify that the tunnel is properly calibrated and functioning.

4.1.2 Loading the Tunnel
4.1.2.1 Arrange the containers and closures to be sterilized on the conveyor belt, ensuring there is space between them for air circulation.
4.1.2.2 Start the conveyor belt and feed the items into

the tunnel.

4.1.3 Sterilization Process
4.1.3.1 Select the appropriate temperature and time settings for the sterilization process.
4.1.3.2 Start the tunnel and monitor the process.
4.1.3.3 Allow the sterilization cycle to complete and ensure the tunnel reaches the required conditions for sterilization.
4.1.3.4 After the cycle is complete, allow the items to exit the tunnel and cool down.

See also  SOP for Product Recalls

4.1.4 Unloading the Tunnel
4.1.4.1 Carefully remove the sterilized items from the conveyor belt.
4.1.4.2 Inspect the items to ensure they are free from contamination and damage.

4.2 Calibration
4.2.1 Daily Check
4.2.1.1 Perform a daily check of the tunnel’s temperature settings and indicators.
4.2.1.2 Record the results in the equipment log.

4.2.2 Monthly Calibration
4.2.2.1 Conduct a full calibration of the sterilization tunnel monthly using standard test methods.
4.2.2.2 Document the calibration results and any adjustments made.

4.3 Maintenance
4.3.1 Routine Maintenance
4.3.1.1 Clean the tunnel and all parts regularly to prevent contamination.
4.3.1.2 Inspect the tunnel for any signs of wear or damage and replace parts as necessary.

See also  SOP for Cleanroom Monitoring System

4.3.2 Troubleshooting
4.3.2.1 If the tunnel displays error messages or fails to reach the required conditions, refer to the manufacturer’s manual for troubleshooting steps.
4.3.2.2 Contact maintenance personnel if the issue cannot be resolved.

5) Abbreviations, if any

QC: Quality Control
SOP: Standard Operating Procedure

6) Documents, if any

Sterilization log
Maintenance log

7) Reference, if any

Manufacturer’s manual for the sterilization tunnel
Regulatory guidelines for equipment calibration and maintenance

8) SOP Version

Version 1.0

Otic (Ear) Dosage Forms Tags:Cleaning validation in otic manufacturing, Ear Drops dosage form SOP, Ear Drops SOP, EarDrops SOP, Environmental monitoring in otic manufacturing, GMP for Ear Drops, GMP for otic products, Otic dosage form calibration SOP, Otic dosage form equipment cleaning SOP, Otic dosage form quality assurance, Otic dosage form SOP, Otic drug complaint handling SOP, Otic drug documentation control SOP, Otic drug in-process control SOP, Otic drug stability testing SOP, Otic manufacturing process SOP, Otic product batch record SOP, Otic product deviation handling SOP, Otic product raw material handling SOP, Otic product self-inspection SOP, Otic product vendor qualification SOP, Otic solution SOP, Otic suspension SOP, Quality control for otic dosage forms, SOP for Ear Drops manufacturing, SOP for otic dosage form returned goods, SOP for otic dosage form training, SOP for otic drug manufacturing, SOP for otic formulation development, SOP for otic product labeling, SOP for otic product packaging, SOP for otic product recalls, SOP for otic product release, SOP for otic product sampling

Post navigation

Previous Post: SOP for Sealing Line for Ointments
Next Post: SOP for Calibration of Measuring Instruments

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