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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: Documentation Control SOP

SOP for Compressed Air Monitoring

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SOP for Compressed Air Monitoring Standard Operating Procedure for Compressed Air Monitoring 1) Purpose This SOP outlines the procedures for monitoring the quality of compressed air used in pharmaceutical manufacturing processes. 2) Scope This SOP applies to the monitoring of compressed air systems throughout the pharmaceutical manufacturing facility to ensure compliance with quality standards and…

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Quality Assurance

SOP for Water System Monitoring

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SOP for Water System Monitoring Standard Operating Procedure for Water System Monitoring 1) Purpose This SOP outlines the procedures for monitoring the pharmaceutical water system to ensure quality and compliance with regulatory standards. 2) Scope This SOP applies to the monitoring of pharmaceutical water systems including purified water (PW), water for injection (WFI), and other…

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Quality Assurance

SOP for HVAC System Monitoring

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SOP for HVAC System Monitoring Standard Operating Procedure for HVAC System Monitoring 1) Purpose This SOP outlines the procedures for monitoring Heating, Ventilation, and Air Conditioning (HVAC) systems in pharmaceutical manufacturing facilities. 2) Scope This SOP applies to the monitoring of HVAC systems throughout the pharmaceutical manufacturing facility to ensure compliance with environmental control requirements….

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Quality Assurance

SOP for HEPA Filter Integrity Testing

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SOP for HEPA Filter Integrity Testing Standard Operating Procedure for HEPA Filter Integrity Testing 1) Purpose This SOP outlines the procedures for conducting HEPA filter integrity testing in cleanrooms or controlled environments. 2) Scope This SOP applies to HEPA filter integrity testing conducted in cleanrooms or areas where high-efficiency particulate air (HEPA) filters are used…

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Quality Assurance

SOP for Microbial Enumeration Testing

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SOP for Microbial Enumeration Testing Standard Operating Procedure for Microbial Enumeration Testing 1) Purpose This SOP outlines the procedures for conducting microbial enumeration testing on pharmaceutical raw materials and products. 2) Scope This SOP applies to microbial enumeration testing of raw materials, intermediate products, and finished pharmaceutical products in the manufacturing facility. 3) Responsibilities The…

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Quality Assurance

SOP for Elemental Impurity Testing

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SOP for Elemental Impurity Testing Standard Operating Procedure for Elemental Impurity Testing 1) Purpose This SOP outlines the procedures for conducting elemental impurity testing on pharmaceutical raw materials and products. 2) Scope This SOP applies to elemental impurity testing of raw materials, intermediate products, and finished pharmaceutical products in the manufacturing facility. 3) Responsibilities The…

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Quality Assurance

SOP for Residual Solvent Testing

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SOP for Residual Solvent Testing Standard Operating Procedure for Residual Solvent Testing 1) Purpose This SOP outlines the procedures for conducting residual solvent testing on pharmaceutical raw materials and products. 2) Scope This SOP applies to residual solvent testing of raw materials, intermediate products, and finished pharmaceutical products in the manufacturing facility. 3) Responsibilities The…

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Quality Assurance

SOP for Impurity Testing

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SOP for Impurity Testing Standard Operating Procedure for Impurity Testing 1) Purpose This SOP outlines the procedures for conducting impurity testing on pharmaceutical raw materials and products. 2) Scope This SOP applies to impurity testing of raw materials, intermediate products, and finished pharmaceutical products in the manufacturing facility. 3) Responsibilities The Quality Control (QC) department…

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Quality Assurance

SOP for Assay Testing

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SOP for Assay Testing Standard Operating Procedure for Assay Testing 1) Purpose This SOP outlines the procedures for conducting assay testing on pharmaceutical raw materials and products. 2) Scope This SOP applies to assay testing of raw materials, intermediate products, and finished pharmaceutical products in the manufacturing facility. 3) Responsibilities The Quality Control (QC) department…

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Quality Assurance

SOP for Identification Tests

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SOP for Identification Tests Standard Operating Procedure for Identification Tests 1) Purpose This SOP outlines the procedures for conducting identification tests on pharmaceutical raw materials and products. 2) Scope This SOP applies to identification testing of raw materials, intermediate products, and finished pharmaceutical products in the manufacturing facility. 3) Responsibilities The Quality Control (QC) department…

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Quality Assurance

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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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