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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: pH measurement of solutions SOP

SOP for Particulate Matter Testing in Liquids

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SOP for Particulate Matter Testing in Liquids Procedure for Particulate Matter Testing in Liquids 1) Purpose The purpose of this SOP is to outline the procedure for testing particulate matter in liquid samples used in pharmaceutical manufacturing to ensure product quality and safety. 2) Scope This SOP applies to all liquid formulations produced within the…

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In-Process Control

SOP for Specific Gravity Testing of Liquids

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SOP for Specific Gravity Testing of Liquids Procedure for Specific Gravity Testing of Liquids 1) Purpose The purpose of this SOP is to outline the procedure for measuring the specific gravity of liquid samples used in pharmaceutical manufacturing to ensure accurate density determination. 2) Scope This SOP applies to all liquid formulations produced within the…

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In-Process Control

SOP for Viscosity Testing of Liquids

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SOP for Viscosity Testing of Liquids Procedure for Viscosity Testing of Liquids 1) Purpose The purpose of this SOP is to outline the procedure for measuring the viscosity of liquid samples used in pharmaceutical manufacturing to ensure consistency and quality control. 2) Scope This SOP applies to all liquid formulations produced within the manufacturing facility…

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In-Process Control

SOP for pH Measurement of Solutions

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SOP for pH Measurement of Solutions Procedure for pH Measurement of Solutions 1) Purpose The purpose of this SOP is to outline the procedure for accurately measuring the pH of solutions used in pharmaceutical manufacturing to ensure consistency and quality. 2) Scope This SOP applies to all solutions used within the manufacturing facility that require…

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In-Process Control

SOP for Uniformity of Dosage Units

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SOP for Uniformity of Dosage Units Procedure for Uniformity of Dosage Units Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the uniformity of dosage units (tablets) to ensure consistent distribution of the active pharmaceutical ingredient (API) among individual units. 2) Scope This SOP applies to all batches of…

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In-Process Control

SOP for Capsule Dissolution Testing

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SOP for Capsule Dissolution Testing Procedure for Capsule Dissolution Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the dissolution of capsules to ensure consistent release of the active pharmaceutical ingredient (API) over a specified time period. 2) Scope This SOP applies to all capsule batches produced within the…

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In-Process Control

SOP for Capsule Disintegration Testing

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SOP for Capsule Disintegration Testing Procedure for Capsule Disintegration Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the disintegration of capsules to ensure they break down into smaller particles or dissolve completely within the specified time frame for effective drug release. 2) Scope This SOP applies to all…

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In-Process Control

SOP for Capsule Content Uniformity

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SOP for Capsule Content Uniformity Procedure for Capsule Content Uniformity Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the content uniformity of capsules to ensure consistent distribution of active pharmaceutical ingredient (API) across all dosage units. 2) Scope This SOP applies to all capsule batches produced within the…

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In-Process Control

SOP for Capsule Weight Variation

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SOP for Capsule Weight Variation Procedure for Capsule Weight Variation Testing 1) Purpose The purpose of this SOP is to outline the procedure for determining the weight variation of capsules to ensure uniformity and compliance with pharmacopeial standards. 2) Scope This SOP applies to all capsule batches produced within the manufacturing facility. 3) Responsibilities Quality…

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In-Process Control

SOP for Tablet Dissolution Testing

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SOP for Tablet Dissolution Testing Procedure for Tablet Dissolution Testing 1) Purpose The purpose of this SOP is to outline the procedure for testing the dissolution of tablets to ensure consistent release of the active pharmaceutical ingredient (API) over a specified time period. 2) Scope This SOP applies to all tablet batches produced within the…

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In-Process Control

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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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