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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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SOPs for Creams V 2.0

Creams: SOP for Accelerated Stability Testing of Cream Formulations – V 2.0

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The purpose of this SOP is to outline the procedure for conducting accelerated stability testing of cream formulations. Accelerated stability testing helps predict the shelf life and stability of cream products by subjecting them to controlled conditions of temperature and humidity. This process is essential for ensuring product efficacy and safety throughout its intended shelf life.

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Creams V 2.0

Creams: SOP for Testing Active Ingredient Content in Creams – V 2.0

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The purpose of this SOP is to define the procedure for testing the active ingredient content in cream formulations. Ensuring the correct amount of active ingredients is critical for the efficacy of the product. This SOP outlines the methods to ensure that the active ingredient content meets the specified levels as per formulation requirements.

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Creams V 2.0

Creams: SOP for Packaging Integrity Testing of Cream Products – V 2.0

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The purpose of this SOP is to define the procedure for packaging integrity testing of cream products. Packaging integrity is crucial to ensuring the product’s quality, safety, and efficacy during storage and transportation. This SOP provides guidelines for testing packaging components, including seals, closures, and containers, to verify their ability to protect the product from contamination and preserve its shelf life.

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Creams V 2.0

Creams: SOP for Water Activity Measurement in Cream Formulations – V 2.0

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The purpose of this SOP is to define the procedure for measuring the water activity (aw) of cream formulations. Water activity is an important parameter in determining the stability, microbial growth potential, and shelf life of cream products. This SOP ensures that the water activity of cream formulations is measured accurately to meet product quality and safety standards.

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Creams V 2.0

Creams: SOP for Preservative Efficacy Testing of Creams – V 2.0

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The purpose of this SOP is to establish a standard procedure for conducting preservative efficacy testing (PET) of cream formulations. The effectiveness of preservatives in a cream formulation is critical for preventing microbial contamination during its shelf life. This test ensures that the preservatives used in the formulation are effective in inhibiting the growth of microorganisms.

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Creams V 2.0

Creams: SOP for Conducting FTIR Analysis of Cream Ingredients – V 2.0

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The purpose of this SOP is to define the procedure for conducting Fourier Transform Infrared (FTIR) analysis of cream ingredients. FTIR analysis is used to identify the chemical composition of active ingredients and excipients in cream formulations. This test ensures the quality and integrity of the ingredients, confirming their authenticity and purity.

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Creams V 2.0

Creams: SOP for Testing Antioxidant Stability in Creams – V 2.0

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The purpose of this SOP is to define the procedure for testing antioxidant stability in cream formulations. Antioxidants are added to cream products to prevent oxidative degradation of active ingredients, which can reduce product efficacy and shelf life. This SOP ensures that the antioxidant content remains stable and effective over time.

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Creams V 2.0

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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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