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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
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SOPs for Ocular (Eye) Dosage Forms

SOP for Cryogenic Storage Equipment

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The purpose of this SOP is to provide guidelines for the proper use and maintenance of cryogenic storage equipment to ensure the safe and effective storage of temperature-sensitive ocular dosage forms.
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Ocular (Eye) Dosage Forms

SOP for Semi-Solid Dosage Form Production

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The purpose of this SOP is to provide guidelines for the production of semi-solid dosage forms, such as ointments, gels, and creams, to ensure consistent quality and compliance with regulatory standards.
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Ocular (Eye) Dosage Forms

SOP for Controlled Release Insert Manufacturing

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The purpose of this SOP is to provide guidelines for the manufacturing of controlled release inserts used in ocular dosage forms, ensuring consistent quality and efficacy.
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Ocular (Eye) Dosage Forms

SOP for Gel Tube Sealing

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The purpose of this SOP is to provide guidelines for the proper sealing of gel tubes to ensure the sterility and integrity of the ocular dosage forms during and after the sealing process.
Click to read the full article.

Ocular (Eye) Dosage Forms

SOP for Ointment Tube Sealing

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The purpose of this SOP is to provide guidelines for the proper sealing of ointment tubes to ensure the sterility and integrity of the ocular dosage forms during and after the sealing process.
Click to read the full article.

Ocular (Eye) Dosage Forms

SOP for Eye Drop Bottle Sealing

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The purpose of this SOP is to provide guidelines for the proper sealing of eye drop bottles to ensure the sterility and integrity of the ocular dosage forms during and after the sealing process.
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Ocular (Eye) Dosage Forms

SOP for Filter Integrity Testing

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The purpose of this SOP is to outline the procedure for performing filter integrity testing to ensure that the sterile filters used in the production of ocular dosage forms are functioning correctly and effectively retaining microorganisms.
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Ocular (Eye) Dosage Forms

SOP for Sterile Filtration

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The purpose of this SOP is to provide guidelines for the sterile filtration process used in the production of ocular dosage forms, ensuring the removal of microorganisms and particulates from the product solutions.
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Ocular (Eye) Dosage Forms

SOP for Cold Room for Raw Material Storage

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The purpose of this SOP is to provide guidelines for the operation, monitoring, and maintenance of the cold room used for the storage of raw materials, particularly those used in the manufacturing of ocular dosage forms, in the pharmaceutical manufacturing facility.
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Ocular (Eye) Dosage Forms

SOP for Refrigerator for Drug Storage

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The purpose of this SOP is to provide guidelines for the operation, monitoring, and maintenance of refrigerators used for the storage of drugs, particularly ocular dosage forms, in the pharmaceutical manufacturing facility.
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Ocular (Eye) Dosage Forms

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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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