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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: CAPA SOP (Corrective and Preventive Actions)

SOP for Specific Gravity Testing

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SOP for Specific Gravity Testing Standard Operating Procedure for Specific Gravity Testing 1) Purpose This SOP outlines the procedures for determining the specific gravity of pharmaceutical liquids or solids. 2) Scope This SOP applies to specific gravity testing of raw materials, intermediate products, and finished pharmaceutical products in the manufacturing facility. 3) Responsibilities The Quality…

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Quality Assurance

Quality Assurance: SOP for Viscosity Testing

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SOP for Viscosity Testing Standard Operating Procedure for Viscosity Testing 1) Purpose This SOP outlines the procedures for determining the viscosity of pharmaceutical liquids or semi-solids. 2) Scope This SOP applies to viscosity testing of raw materials, intermediate products, and finished pharmaceutical products in the manufacturing facility. 3) Responsibilities The Quality Control (QC) department is…

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Quality Assurance

SOP for pH Determination

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SOP for pH Determination Standard Operating Procedure for pH Determination 1) Purpose This SOP outlines the procedures for determining the pH of pharmaceutical raw materials and products. 2) Scope This SOP applies to pH determination 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 Moisture Content Determination

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SOP for Moisture Content Determination Standard Operating Procedure for Moisture Content Determination 1) Purpose This SOP outlines the procedures for determining the moisture content of pharmaceutical raw materials and products. 2) Scope This SOP applies to moisture content determination of raw materials, intermediate products, and finished pharmaceutical products in the manufacturing facility. 3) Responsibilities The…

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Quality Assurance

SOP for Friability Testing of Tablets

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SOP for Friability Testing of Tablets Standard Operating Procedure for Friability Testing of Tablets 1) Purpose This SOP outlines the procedures for conducting friability testing on pharmaceutical tablets to assess their resistance to abrasion and impact. 2) Scope This SOP applies to friability testing of tablets manufactured in the pharmaceutical facility. 3) Responsibilities The Quality…

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Quality Assurance

SOP for Hardness Testing of Tablets

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SOP for Hardness Testing of Tablets Standard Operating Procedure for Hardness Testing of Tablets 1) Purpose This SOP outlines the procedures for conducting hardness testing on pharmaceutical tablets to ensure mechanical strength and quality. 2) Scope This SOP applies to hardness testing of tablets manufactured in the pharmaceutical facility. 3) Responsibilities The Quality Control (QC)…

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Quality Assurance

SOP for Disintegration Testing

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SOP for Disintegration Testing Standard Operating Procedure for Disintegration Testing 1) Purpose This SOP outlines the procedures for conducting disintegration testing on pharmaceutical solid oral dosage forms to assess their disintegration characteristics. 2) Scope This SOP applies to disintegration testing of tablets and capsules manufactured in the pharmaceutical facility. 3) Responsibilities The Quality Control (QC)…

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Quality Assurance

SOP for Dissolution Testing

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SOP for Dissolution Testing Standard Operating Procedure for Dissolution Testing 1) Purpose This SOP outlines the procedures for conducting dissolution testing on pharmaceutical products to assess drug release characteristics. 2) Scope This SOP applies to dissolution testing of solid oral dosage forms, including tablets and capsules, manufactured in the pharmaceutical facility. 3) Responsibilities The Quality…

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Quality Assurance

SOP for Content Uniformity Testing

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SOP for Content Uniformity Testing Standard Operating Procedure for Content Uniformity Testing 1) Purpose This SOP outlines the procedures for conducting content uniformity testing on pharmaceutical products to ensure consistency and compliance with dosage specifications. 2) Scope This SOP applies to content uniformity testing of solid oral dosage forms, including tablets and capsules, manufactured in…

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Quality Assurance

SOP for Weight Variation Testing

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SOP for Weight Variation Testing Standard Operating Procedure for Weight Variation Testing 1) Purpose This SOP outlines the procedures for conducting weight variation testing on solid oral dosage forms to ensure uniformity and compliance with dosage specifications. 2) Scope This SOP applies to weight variation testing of solid oral dosage forms such as tablets and…

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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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