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
  • 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 Tubing Sealer for Ointments

Posted on By

SOP for Tubing Sealer for Ointments

Standard Operating Procedure for Ointment Tubing Sealer Operation

1) Purpose

The purpose of this SOP is to provide a detailed procedure for the operation and maintenance of the Tubing Sealer for Ointments used in the manufacturing of ocular dosage forms.

2) Scope

This SOP applies to the Tubing Sealer for Ointments used in the production of sterile ocular dosage forms within the pharmaceutical manufacturing facility.

3) Responsibilities

The responsibilities include the operation, cleaning, and maintenance of the Tubing Sealer for Ointments. The machine operator is responsible for following the procedure, and the maintenance team is responsible for regular maintenance and calibration.

See also  SOP for Ointment Preparation System

4) Procedure

4.1 Preparation

  1. Ensure the tubing sealer and surrounding area are clean and sanitized.
  2. Verify that all necessary materials and equipment are available and within expiry dates.
  3. Check that the tubing sealer is connected to the appropriate power supply and is functioning properly.

4.2 Operation

  1. Turn on the tubing sealer and allow it to warm up as per the manufacturer’s instructions.
  2. Load the ointment tubes into the sealer’s feed system.
  3. Adjust the sealing parameters (temperature, pressure, time) according to the specific ointment tube being sealed.
  4. Initiate the sealing process by pressing the start button.
  5. Monitor the sealing process to ensure that the seals are uniform and free from defects.
  6. Once sealing
is complete, inspect the sealed tubes for integrity and quality.
  • Collect the sealed tubes and transfer them to the designated storage area.
  • 4.3 Post-Operation

    1. Turn off the tubing sealer and disconnect it from the power supply.
    2. Clean the sealer and surrounding area according to the cleaning procedure.
    3. Record the operation details in the equipment logbook.

    4.4 Maintenance

    1. Regularly inspect the tubing sealer for any signs of wear or damage.
    2. Lubricate moving parts as per the manufacturer’s recommendations.
    3. Perform calibration checks as per the schedule to ensure consistent sealing quality.
    4. Replace any worn-out parts promptly to maintain the efficiency of the sealer.

    5) Abbreviations, if any

    None

    6) Documents, if any

    1. Equipment logbook
    2. Maintenance record
    3. Calibration record

    7) Reference, if any

    GMP Guidelines for pharmaceutical production and equipment handling.

    8) SOP Version

    Version 1.0

    See also  SOP for Clean Room Particle Counter
    Ocular (Eye) Dosage Forms Tags:Aseptic processing, Bioavailability in ocular drugs, Blow-fill-seal technology, Cleanroom standards, Conjunctival inserts, Contact lenses drug delivery, Drug stability testing, Ethylene oxide sterilization, Eye drops SOP, Gamma sterilization, Heat sterilization, HEPA filtration, Intraocular implants, Intraocular injections, Microemulsions in ophthalmics, Mucoadhesive polymers, Multidose ophthalmic bottles, ocular dosage forms, Ocular drug delivery, Ointment preparation, Ophthalmic formulations, Ophthalmic gels, Ophthalmic suspensions, Ophthalmic viscosity, Preservative-free formulations, Solubility issues, SOP for Ocular Dosage Forms, Sterile filtration, Sterile solutions, Sterility testing, Terminal sterilization, Topical ocular drugs

    Post navigation

    Previous Post: SOP for Assay of Active Ingredient in Granules
    Next Post: SOP for Equipment Calibration and Maintenance

    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