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Revised SOPs for Aerosols V 2.0

Aerosol: SOP for Monitoring Fill Weights During Manufacturing – V 2.0

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This Standard Operating Procedure (SOP) defines the process for monitoring fill weights during the aerosol product manufacturing process. The objective is to ensure that each aerosol container is filled with the correct amount of product to meet regulatory and quality standards. Monitoring fill weights helps to maintain product consistency, minimize overfilling or underfilling, and ensure compliance with product labeling claims.
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Aerosols V 2.0

Aerosol: SOP for Valve Placement and Crimp Testing – V 2.0

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This Standard Operating Procedure (SOP) outlines the process for valve placement and crimp testing of aerosol products. The objective is to ensure that the valve is correctly positioned and securely crimped onto the aerosol can, preventing leakage and ensuring the product functions as intended. Valve placement and crimp testing are critical to product safety and performance, as they ensure proper dispensing and the integrity of the product packaging.
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Aerosols V 2.0

Aerosol: SOP for Conducting Propellant-Filling Checks – V 2.0

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This Standard Operating Procedure (SOP) outlines the process for conducting propellant-filling checks during the aerosol manufacturing process. The objective is to verify that the correct amount of propellant is filled into each aerosol can, ensuring consistent product performance, safety, and compliance with regulatory standards. Proper propellant filling is crucial for the can’s pressurization and dispensing efficiency.
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Aerosols V 2.0

Aerosol: SOP for Visual Inspection of Aerosol Containers – V 2.0

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This Standard Operating Procedure (SOP) defines the process for conducting visual inspection of aerosol containers to ensure that they meet the required quality and safety standards. The objective is to identify any defects, such as dents, scratches, corrosion, improper sealing, or mislabeling, before the containers proceed to the next stage of packaging and distribution. Visual inspection ensures that only conforming products are released for sale, maintaining product quality and compliance with regulatory requirements.
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Aerosols V 2.0

Aerosol: SOP for Checking Crimp Diameter During Manufacturing – V 2.0

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This Standard Operating Procedure (SOP) defines the process for checking the crimp diameter of aerosol cans during the manufacturing process. The objective is to ensure that the crimp on the aerosol container is properly applied, ensuring the integrity and safety of the product. A proper crimp diameter ensures that the valve is securely attached and prevents leakage or other product failures. The test also helps maintain uniformity and product quality throughout production.
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Aerosols V 2.0

Aerosol: SOP for In-Line Monitoring of Spray Performance – V 2.0

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This Standard Operating Procedure (SOP) outlines the process for in-line monitoring of spray performance during aerosol manufacturing. The objective is to continuously monitor the spray characteristics of aerosol products to ensure that they meet the required specifications for performance, consistency, and quality. Spray performance monitoring ensures that the aerosol product delivers the desired spray pattern, flow rate, and droplet size for effective use.
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Aerosols V 2.0

Aerosol: SOP for Collecting In-Process Samples for Analysis – V 2.0

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This Standard Operating Procedure (SOP) defines the process for collecting in-process samples during aerosol manufacturing. The objective is to ensure that samples are collected at defined stages of the manufacturing process for quality control analysis. In-process sampling is critical for identifying any issues early in the production process and ensuring that the final product meets the required specifications.
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Aerosols V 2.0

Aerosol: SOP for Reconciliation of In-Process Components – V 2.0

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This Standard Operating Procedure (SOP) outlines the process for the reconciliation of in-process components during aerosol manufacturing. The objective is to ensure that all components, such as raw materials, propellants, and aerosol containers, are accounted for during production. Proper reconciliation ensures that the correct quantities of materials are used, minimizing waste, preventing shortages, and maintaining compliance with regulatory requirements.
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Aerosols V 2.0

Aerosol: SOP for Monitoring Batch Yield During Production – V 2.0

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This Standard Operating Procedure (SOP) describes the process for monitoring batch yield during aerosol production. The objective is to ensure that the amount of product produced aligns with the expected yield for the batch, minimizing waste, identifying inefficiencies, and ensuring that the production process is operating within specified parameters. Monitoring batch yield ensures that the production process meets efficiency goals and regulatory standards.
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Aerosols V 2.0

Aerosol: SOP for Documenting In-Process Control Activities – V 2.0

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This Standard Operating Procedure (SOP) provides guidelines for documenting in-process control activities during aerosol manufacturing. The purpose is to ensure that all control activities, including inspections, testing, and process monitoring, are accurately documented to verify compliance with quality standards and regulatory requirements. Proper documentation helps in traceability, auditing, and process improvements.
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Aerosols 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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