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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Revised SOPs for Aerosols V 2.0

Aerosol: SOP for Receiving Raw Materials for Aerosol Dosage Forms – V 2.0

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This Standard Operating Procedure (SOP) outlines the procedures for receiving raw materials used in the manufacture of aerosol dosage forms. It ensures that all materials meet the required quality standards and are received in compliance with Good Manufacturing Practices (GMP). This SOP is essential for maintaining the integrity of the materials used and ensuring that only approved, quality raw materials are used in the manufacturing process.
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Aerosols V 2.0

Aerosol: SOP for Weighing and Dispensing Raw Materials – V 2.0

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This Standard Operating Procedure (SOP) outlines the procedures for the accurate weighing and dispensing of raw materials used in the manufacture of aerosol dosage forms. It ensures that the correct quantities of raw materials are dispensed in compliance with Good Manufacturing Practices (GMP) and are suitable for use in production.
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Aerosols V 2.0

Aerosol: SOP for Handling Controlled Substances in Aerosol Manufacturing – V 2.0

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This Standard Operating Procedure (SOP) outlines the procedures for the safe and compliant handling of controlled substances in the aerosol manufacturing process. It ensures that all controlled substances are handled, stored, and disposed of according to the relevant regulatory requirements and GMP standards to prevent misuse, contamination, or unauthorized access.
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Aerosols V 2.0

Aerosol: SOP for Labeling Dispensed Materials – V 2.0

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This Standard Operating Procedure (SOP) outlines the procedures for labeling dispensed materials used in aerosol manufacturing. It ensures that all dispensed materials are correctly labeled with relevant product information, including batch numbers, expiration dates, and other necessary details, in compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
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Aerosols V 2.0

Aerosol: SOP for Storage of Dispensed Materials – V 2.0

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This Standard Operating Procedure (SOP) outlines the procedures for the proper storage of dispensed materials used in aerosol manufacturing. It ensures that materials are stored securely and under the correct conditions to maintain their quality, safety, and compliance with Good Manufacturing Practices (GMP) until they are used in production.
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Aerosols V 2.0

Aerosol: SOP for Verifying Weighed Quantities of Raw Materials – V 2.0

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This Standard Operating Procedure (SOP) outlines the process for verifying the accuracy of the quantities of raw materials weighed during the dispensing process in aerosol manufacturing. It ensures that the correct amounts of raw materials are used, maintaining the quality of the final product and compliance with Good Manufacturing Practices (GMP).
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Aerosols V 2.0

Aerosol: SOP for Handling and Disposal of Expired Raw Materials – V 2.0

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This Standard Operating Procedure (SOP) outlines the process for handling and disposing of expired raw materials used in aerosol manufacturing. It ensures that expired materials are properly segregated, documented, and disposed of in compliance with Good Manufacturing Practices (GMP) and regulatory requirements to prevent contamination or misuse.
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Aerosols V 2.0

Aerosol: SOP for Environmental Monitoring During Material Dispensing – V 2.0

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This Standard Operating Procedure (SOP) describes the process for environmental monitoring during material dispensing in aerosol manufacturing. It ensures that the dispensing area meets the required environmental conditions to maintain the integrity and quality of materials being dispensed, and complies with Good Manufacturing Practices (GMP) and regulatory requirements.
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Aerosols V 2.0

Aerosol: SOP for Cross-Contamination Prevention in Dispensing Areas – V 2.0

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This Standard Operating Procedure (SOP) outlines the procedures to prevent cross-contamination in dispensing areas during aerosol manufacturing. It ensures that raw materials are dispensed in a manner that prevents the unintended mixing or contamination of materials, which is critical to maintaining product quality, safety, and compliance with Good Manufacturing Practices (GMP).
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Aerosols V 2.0

Aerosol: SOP for Calibration of Weighing Balances in Dispensing Areas – V 2.0

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This Standard Operating Procedure (SOP) defines the procedures for the calibration of weighing balances in dispensing areas within aerosol manufacturing. It ensures that weighing equipment is properly calibrated and maintained to ensure accurate and consistent measurements of raw materials used in the production process, in compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
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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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