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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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SOPs for In-Process Control

In-process testing plays a pivotal role in pharmaceutical manufacturing, ensuring the quality, safety, and efficacy of pharmaceutical products. By conducting various tests throughout the manufacturing process, manufacturers can monitor critical parameters and identify any deviations or issues early on. In-process testing allows for real-time monitoring of key quality attributes such as content uniformity, dissolution rates, and microbiological purity, among others. This proactive approach helps to prevent defects, minimize batch failures, and ensure that products consistently meet regulatory requirements and quality standards. Moreover, in-process testing enables manufacturers to implement corrective actions promptly, improving process efficiency and reducing the risk of producing substandard or unsafe products. Ultimately, the importance of in-process testing in pharmaceuticals lies in its ability to uphold product quality, safeguard patient health, and maintain the integrity of the pharmaceutical industry as a whole.

SOP for Syringeability Testing in Injectables

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SOP for Syringeability Testing in Injectables Procedure for Syringeability Testing in Injectables 1) Purpose The purpose of this SOP is to outline the procedure for evaluating the syringeability of injectable pharmaceutical products to ensure ease of administration and product quality. 2) Scope This SOP applies to all injectable pharmaceutical products manufactured within the facility that…

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In-Process Control

SOP for Sedimentation Volume Testing in Suspensions

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SOP for Sedimentation Volume Testing in Suspensions Procedure for Sedimentation Volume Testing in Suspensions 1) Purpose The purpose of this SOP is to outline the procedure for determining the sedimentation volume of pharmaceutical suspensions to assess stability and uniformity. 2) Scope This SOP applies to all pharmaceutical suspensions manufactured within the facility that require sedimentation…

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In-Process Control

SOP for Redispersibility Testing in Suspensions

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SOP for Redispersibility Testing in Suspensions Procedure for Redispersibility Testing in Suspensions 1) Purpose The purpose of this SOP is to outline the procedure for evaluating the redispersibility of pharmaceutical suspensions after storage to ensure uniformity and quality. 2) Scope This SOP applies to all pharmaceutical suspensions manufactured within the facility that require redispersibility testing…

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In-Process Control

SOP for Particle Size Distribution in Suspensions

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SOP for Particle Size Distribution in Suspensions Procedure for Particle Size Distribution in Suspensions 1) Purpose The purpose of this SOP is to outline the procedure for determining the particle size distribution in pharmaceutical suspensions to ensure product quality and consistency. 2) Scope This SOP applies to all pharmaceutical suspensions manufactured within the facility that…

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In-Process Control

SOP for Viscosity Testing in Semisolids

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SOP for Viscosity Testing in Semisolids Procedure for Viscosity Testing in Semisolids 1) Purpose The purpose of this SOP is to outline the procedure for measuring the viscosity of semisolid pharmaceutical formulations to ensure consistency and quality. 2) Scope This SOP applies to all semisolid formulations (e.g., creams, ointments, gels) manufactured within the facility that…

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In-Process Control

SOP for Spreadability Testing in Semisolids

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SOP for Spreadability Testing in Semisolids Procedure for Spreadability Testing in Semisolids 1) Purpose The purpose of this SOP is to outline the procedure for testing the spreadability of semisolid pharmaceutical formulations to assess their ease of application and consistency. 2) Scope This SOP applies to all semisolid formulations (e.g., creams, ointments, gels) manufactured within…

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In-Process Control

SOP for Homogeneity Testing in Creams and Ointments

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SOP for Homogeneity Testing in Creams and Ointments Procedure for Homogeneity Testing in Creams and Ointments 1) Purpose The purpose of this SOP is to outline the procedure for testing the homogeneity of creams and ointments to ensure uniform distribution of active pharmaceutical ingredients (APIs) and excipients. 2) Scope This SOP applies to all creams…

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In-Process Control

SOP for pH Determination in Semisolids

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SOP for pH Determination in Semisolids Procedure for pH Determination in Semisolids 1) Purpose The purpose of this SOP is to outline the procedure for determining the pH of semisolid pharmaceutical formulations to ensure their quality and consistency. 2) Scope This SOP applies to all semisolid formulations (e.g., creams, ointments, gels) manufactured within the facility…

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In-Process Control

In-Process Control: SOP for Visual Inspection of Injectable Products

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SOP for Visual Inspection of Injectable Products Procedure for Visual Inspection of Injectable Products 1) Purpose The purpose of this SOP is to outline the procedure for visually inspecting injectable products to ensure they meet quality standards and are free from visible defects. 2) Scope This SOP applies to all injectable products manufactured within the…

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In-Process Control

In-Process Control: SOP for Leak Testing of Sealed Containers

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SOP for Leak Testing of Sealed Containers Procedure for Leak Testing of Sealed Containers 1) Purpose The purpose of this SOP is to outline the procedure for conducting leak testing on sealed containers to ensure their integrity and prevent leakage of pharmaceutical products. 2) Scope This SOP applies to all types of sealed containers (e.g.,…

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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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