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SOP for Eye Drop Preparation Tank

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SOP for Eye Drop Preparation Tank

Standard Operating Procedure for Eye Drop Preparation Tank

1) Purpose

The purpose of this SOP is to provide a detailed procedure for the operation and maintenance of the Eye Drop Preparation Tank used in the manufacturing of ocular dosage forms.

2) Scope

This SOP applies to the Eye Drop Preparation Tank 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 Eye Drop Preparation Tank. The equipment operator is responsible for following the procedure, and the maintenance team is responsible for regular maintenance and calibration.

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4) Procedure

4.1 Preparation

  1. Ensure the eye drop preparation tank and surrounding area are clean and sanitized.
  2. Verify that all necessary materials (active pharmaceutical ingredients, preservatives) and equipment are available and within expiry dates.
  3. Check that the eye drop preparation tank is properly connected to utilities (water, steam, air, etc.) if required.

4.2 Operation

  1. Turn on the eye drop preparation tank and verify that the temperature and mixing settings are appropriate for the eye drop formulation.
  2. Add the required raw materials into the tank according to the batch formulation.
  3. Start the mixing process as per the specified parameters.
  4. Monitor the temperature and mixing process to ensure the eye drop formulation
is homogenous.
  • Once the eye drop preparation is complete, stop the mixing process.
  • 4.3 Post-Operation

    1. Transfer the prepared eye drops to the designated storage container or directly to the filling machine, if applicable.
    2. Clean the eye drop preparation tank and all associated equipment thoroughly as per the cleaning procedure.
    3. Record the details of the eye drop preparation (batch number, quantity produced, any deviations) in the batch record logbook.

    4.4 Maintenance

    1. Regularly inspect the eye drop preparation tank for cleanliness and signs of wear.
    2. Perform preventive maintenance tasks such as checking seals, lubricating moving parts, and inspecting heating elements.
    3. Calibrate temperature controls periodically to maintain process accuracy.
    4. Replace any worn-out parts or components as per the maintenance schedule.

    5) Abbreviations, if any

    None

    6) Documents, if any

    1. Batch record 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

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    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

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    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

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    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.

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