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SOP Guide for Pharma

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SOPs for Creams V 2.0

Creams: SOP for In-Line Filtration of Creams before Packing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for in-line filtration of creams before packing. In-line filtration ensures that the cream is free from any particulate matter, undissolved ingredients, or contaminants that may have been introduced during the manufacturing process. This step is crucial to maintain the quality, consistency, and safety of the final product before it is packed and distributed.

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Creams V 2.0

Creams: SOP for Batch Coding and Tracking during Cream Manufacturing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to establish the process for batch coding and tracking during the manufacturing of cream products. Batch coding is a critical part of traceability in the manufacturing process, enabling the identification of each batch of product for quality control, inventory management, and regulatory compliance. This SOP ensures that all batch codes are correctly assigned, tracked, and documented during the production process.

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Creams V 2.0

Creams: SOP for Manufacturing Aqueous Cream Bases – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to outline the process for manufacturing aqueous cream bases. Aqueous cream bases are essential in cream formulations, serving as the primary vehicle for active ingredients and ensuring the desired texture and stability. This SOP defines the procedures for preparing the aqueous cream base to ensure that the final product meets all quality standards, including consistency, viscosity, and stability.

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Creams V 2.0

Creams: SOP for Adding Heat-Sensitive Ingredients in Cream Formulations – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for adding heat-sensitive ingredients to cream formulations during production. Heat-sensitive ingredients, such as vitamins, essential oils, and certain active ingredients, may degrade or lose efficacy if exposed to high temperatures. This SOP ensures that such ingredients are added at the correct stage of production, maintaining the integrity and effectiveness of the final cream product.

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Creams V 2.0

Creams: SOP for Using Antioxidants in Cream Manufacturing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for using antioxidants in cream manufacturing. Antioxidants are commonly added to cream formulations to prevent oxidation and prolong the shelf life of the product. This SOP ensures that antioxidants are added at the correct stage of production to maintain the stability, appearance, and effectiveness of the final cream product.

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Creams V 2.0

Creams: SOP for Environmental Monitoring in Manufacturing Areas – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to establish the guidelines for environmental monitoring in manufacturing areas of the Creams Department. This monitoring ensures that the manufacturing environment is maintained within the required standards for cleanliness, temperature, humidity, and air quality, which are crucial to product quality, safety, and compliance with GMP (Good Manufacturing Practices).

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Creams V 2.0

Creams: SOP for Bulk Transfer of Creams to Filling Machines – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to outline the procedure for the bulk transfer of creams to filling machines. Proper bulk transfer is essential to ensure that cream products are transferred in a hygienic, safe, and controlled manner to the filling machines without contamination or loss of product quality. This SOP ensures that the bulk cream is handled in compliance with GMP standards and the required quality specifications.

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Creams V 2.0

Creams: SOP for Handling Deviations during Manufacturing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the steps for handling deviations that may occur during the manufacturing process in the Creams Department. Deviations can arise due to unexpected changes in equipment, materials, or process conditions. This SOP ensures that all deviations are identified, assessed, documented, and resolved in a timely and systematic manner to prevent any negative impact on product quality, safety, and compliance with regulatory standards.

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Creams V 2.0

Creams: SOP for Preventing Cross-Contamination in Cream Manufacturing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to establish guidelines and procedures to prevent cross-contamination during cream manufacturing. Cross-contamination can occur when materials, equipment, or surfaces come into contact with contaminants, leading to the presence of unwanted substances in the product. This SOP ensures that all necessary steps are followed to minimize risks, maintain product integrity, and comply with Good Manufacturing Practices (GMP).

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Creams V 2.0

Creams: SOP for Cleaning Manufacturing Tanks for Creams – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for cleaning manufacturing tanks used in the production of creams. Cleaning of manufacturing tanks is critical to prevent cross-contamination, ensure product quality, and comply with Good Manufacturing Practices (GMP). This SOP outlines the cleaning procedures to ensure that tanks are sanitized and ready for the next production run.

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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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