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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: Content Uniformity Testing

SOP for Density Testing

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Standard Operating Procedure for Density Testing   Purpose The purpose of this SOP is to outline the procedures for conducting density testing during the liquid oral manufacturing process to ensure the proper formulation and quality of the product. Scope This SOP applies to all personnel involved in liquid oral manufacturing, specifically those responsible for density…

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In-Process Control

In-Process Control: SOP for Tablet Hardness Testing 

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Standard Operating Procedure for Hardness Testing   Purpose The purpose of this SOP is to define the procedures for conducting hardness testing during the tablet manufacturing process to ensure the mechanical strength and integrity of capsules. Scope This SOP applies to all personnel involved in tablet manufacturing, specifically those responsible for conducting hardness testing. Responsibilities…

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In-Process Control

SOP for Granule Size Distribution

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Standard Operating Procedure for Granule Size Distribution Purpose The purpose of this SOP is to define the procedures for determining granule size distribution during the tablet/ capsule manufacturing process to ensure product quality and consistency. Scope This SOP applies to all personnel involved in the tablet/ capsule manufacturing process, specifically those responsible for assessing granule…

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In-Process Control

In-Process Control: SOP for Blend Uniformity Testing

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Standard Operating Procedure for Blend Uniformity Testing   Purpose The purpose of this SOP is to outline the procedures for conducting blend uniformity testing during the tablet/ capsule manufacturing process to ensure homogeneity and consistency of the blend. Scope This SOP applies to all personnel involved in the tablet/ capsule manufacturing process, specifically those responsible for…

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In-Process Control

In-Process Control: SOP for pH Testing 

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Standard Operating Procedure for pH Testing   Purpose The purpose of this SOP is to outline the procedures for conducting pH testing during the tablet/ capsule manufacturing process to ensure the acidity or alkalinity of the tablets / capsule. Scope This SOP applies to all personnel involved in tablet manufacturing, specifically those responsible for pH…

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In-Process Control

In-Process Control: SOP for Dissolution Testing 

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Standard Operating Procedure for Dissolution Testing   Purpose The purpose of this SOP is to outline the procedures for conducting dissolution testing during the Capsule/ tablet manufacturing process to ensure proper release of the active pharmaceutical ingredient (API). Scope This SOP applies to all personnel involved in capsule/ tablet manufacturing, specifically those responsible for dissolution…

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In-Process Control

SOP for Disintegration Testing of Tablets

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Standard Operating Procedure for Tablet Disintegration Testing   Purpose The purpose of this SOP is to outline the procedures for conducting disintegration testing during the tablet manufacturing process to ensure proper breakdown and dissolution of tablets. Scope This SOP applies to all personnel involved in tablet manufacturing, specifically those responsible for disintegration testing. Responsibilities Quality…

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In-Process Control

SOP for in-process Weight Variation

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Standard Operating Procedure for in-process Weight Variation Testing   Purpose The purpose of this SOP is to outline the procedures for conducting weight variation testing during the tablet/ capsule manufacturing process to ensure uniformity and consistency of capsule/ tablet weight. Scope This SOP applies to all personnel involved in capsule/ tablet manufacturing, specifically those responsible…

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In-Process Control

SOP for In-Process Friability Testing

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Standard Operating Procedure for in-process Friability Testing Purpose The purpose of this SOP is to outline the procedures for conducting friability testing during the tablet manufacturing process to assess the durability and quality of tablets. Scope This SOP applies to all personnel involved in tablet manufacturing, specifically those responsible for friability testing. Responsibilities Quality Control…

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In-Process Control

SOP for Determination of Moisture Content

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Standard Operating Procedure for Moisture Content Determination in Manufacturing   Purpose The purpose of this SOP is to outline the procedures for determining moisture content during the tablet manufacturing process to ensure product quality, stability, and compliance with regulatory requirements. Scope This SOP applies to all personnel involved in the tablet manufacturing process, particularly those…

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In-Process Control

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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