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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 Temperature Control System

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The purpose of this SOP is to establish procedures for the operation, monitoring, and maintenance of the temperature control system used in the manufacturing of ocular dosage forms to ensure consistent temperature conditions that meet regulatory standards.
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Ocular (Eye) Dosage Forms

SOP for Environmental Control System

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The purpose of this SOP is to establish procedures for the operation, monitoring, and maintenance of the environmental control system used in the manufacturing of ocular dosage forms to ensure a controlled environment that meets regulatory standards.
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Ocular (Eye) Dosage Forms

SOP for Waste Disposal System

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The purpose of this SOP is to establish procedures for the proper disposal of waste generated during the manufacturing of ocular dosage forms to ensure compliance with environmental regulations and maintain a clean and safe manufacturing environment.
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Ocular (Eye) Dosage Forms

SOP for Water Purification System

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The purpose of this SOP is to establish procedures for the operation, maintenance, and monitoring of the water purification system used in the manufacturing of ocular dosage forms to ensure the production of high-quality purified water that meets regulatory standards.
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Ocular (Eye) Dosage Forms

SOP for Sanitization System for Equipment

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The purpose of this SOP is to establish procedures for the sanitization of equipment used in the manufacturing of ocular dosage forms to prevent contamination, maintain cleanliness, and ensure product quality and safety.
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Ocular (Eye) Dosage Forms

SOP for Air Filtration System

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The purpose of this SOP is to establish procedures for the operation and maintenance of the air filtration system in the manufacturing of ocular dosage forms to ensure a controlled and clean environment, free from airborne contaminants.
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Ocular (Eye) Dosage Forms

SOP for Sanitization System for Manufacturing Area

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The purpose of this SOP is to establish procedures for the sanitization of manufacturing areas used in the production of ocular dosage forms to ensure microbial control, prevent contamination, and maintain a clean and safe environment.
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Ocular (Eye) Dosage Forms

Ocular (Eye) Dosage Forms: SOP for Sanitization System for Equipment

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The purpose of this SOP is to establish procedures for the sanitization of equipment used in the manufacturing of ocular dosage forms to ensure microbial control, prevent contamination, and maintain product quality and safety.
Click to read the full article.

Ocular (Eye) Dosage Forms

SOP for Cleaning System for Equipment

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The purpose of this SOP is to define the procedures for cleaning equipment used in the manufacturing of ocular dosage forms to ensure cleanliness, prevent cross-contamination, and maintain product quality.
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Ocular (Eye) Dosage Forms

SOP for Handling System for Raw Materials

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The purpose of this SOP is to establish guidelines for the proper handling of raw materials used in the manufacturing of ocular dosage forms, ensuring safe and efficient material handling practices.
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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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