Skip to content
  • Clinical Studies
  • Schedule M
  • Stability Studies
  • Pharma GMP
  • Pharma Tips
  • Pharma Books
  • Pharma Validation
  • Pharma Regulatory

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

Revised SOPs for Aerosols V 2.0

Aerosol: SOP for Cleaning Aerosol Filling Machines – V 2.0

Posted on By

This Standard Operating Procedure (SOP) defines the procedure for cleaning aerosol filling machines to ensure product quality, machine hygiene, and compliance with regulatory standards. The objective of this SOP is to ensure the effective removal of product residue, cleaning agents, and contaminants from filling machines, which helps maintain the integrity of aerosol products and reduces the risk of cross-contamination between production batches.
Click to read the full article.

Aerosols V 2.0

Aerosol: SOP for Cleaning Crimping Machines After Use – V 2.0

Posted on By

This Standard Operating Procedure (SOP) defines the procedure for cleaning crimping machines used in aerosol manufacturing after each use. The objective of this SOP is to ensure the effective removal of product residue, contaminants, and any oils or lubricants from the crimping machine components, maintaining both machine hygiene and the quality of the aerosol products. Proper cleaning of the crimping machines prevents cross-contamination and ensures compliance with Good Manufacturing Practices (GMP).
Click to read the full article.

Aerosols V 2.0

Aerosol: SOP for Validating Cleaning Processes for Machines – V 2.0

Posted on By

This Standard Operating Procedure (SOP) defines the process for validating cleaning processes for aerosol manufacturing machines. The purpose of this SOP is to ensure that cleaning activities are effective in removing product residues, cleaning agents, and other contaminants from machine components to prevent cross-contamination between batches and ensure product safety. The validation of cleaning processes is a key part of maintaining compliance with GMP standards and ensuring the quality of aerosol products.
Click to read the full article.

Aerosols V 2.0

Aerosol: SOP for Handling and Disposal of Cleaning Agents – V 2.0

Posted on By

This Standard Operating Procedure (SOP) defines the process for the proper handling, storage, and disposal of cleaning agents used in aerosol manufacturing. The objective of this SOP is to ensure that cleaning agents are handled safely to minimize exposure risks to personnel, prevent environmental contamination, and comply with regulatory requirements. Proper disposal procedures are critical for maintaining a safe and compliant manufacturing environment.
Click to read the full article.

Aerosols V 2.0

Aerosol: SOP for Cleaning Validation Records – V 2.0

Posted on By

This Standard Operating Procedure (SOP) outlines the requirements for the documentation and maintenance of cleaning validation records in aerosol manufacturing. The objective of this SOP is to ensure that all cleaning validation activities are thoroughly documented, traceable, and compliant with regulatory standards. Proper documentation of cleaning validation records helps ensure product safety, quality, and compliance with Good Manufacturing Practices (GMP) standards.
Click to read the full article.

Aerosols V 2.0

Aerosol: SOP for Cleaning Propellant Filling Lines – V 2.0

Posted on By

This Standard Operating Procedure (SOP) outlines the process for cleaning propellant filling lines in aerosol manufacturing. The purpose of this SOP is to ensure the effective removal of product residues, propellant remnants, and contaminants from the filling lines after each production run. Proper cleaning of the propellant filling lines is essential to prevent cross-contamination between product batches and ensure compliance with Good Manufacturing Practices (GMP).
Click to read the full article.

Aerosols V 2.0

Aerosol: SOP for Cleaning Storage Tanks for Aerosol Formulations – V 2.0

Posted on By

This Standard Operating Procedure (SOP) defines the steps for cleaning storage tanks used for aerosol formulations to ensure the safe production of high-quality aerosol products. The objective of this SOP is to prevent cross-contamination between batches and ensure that tanks are free from any residues that could affect the quality, safety, and efficacy of the formulations. Effective cleaning is vital to meeting GMP standards and regulatory requirements.
Click to read the full article.

Aerosols V 2.0

Aerosol: SOP for Cleaning and Sanitizing Small Tools in Manufacturing – V 2.0

Posted on By

This Standard Operating Procedure (SOP) outlines the process for cleaning and sanitizing small tools used in aerosol manufacturing. The objective is to ensure that tools are free from contaminants, product residues, and cleaning agents, which could affect the quality and safety of aerosol products. Regular cleaning and sanitization of small tools is essential to comply with Good Manufacturing Practices (GMP) and to maintain product integrity.
Click to read the full article.

Aerosols V 2.0

Aerosol: SOP for Visual Inspection of Cleaned Machines – V 2.0

Posted on By

This Standard Operating Procedure (SOP) outlines the steps for conducting a visual inspection of cleaned machines used in aerosol manufacturing. The objective is to verify that all machines and equipment have been thoroughly cleaned, free from contaminants, residues, and cleaning agents, ensuring that they are ready for the next production run. This inspection is crucial to maintaining product quality and ensuring compliance with Good Manufacturing Practices (GMP).
Click to read the full article.

Aerosols V 2.0

Aerosol: SOP for Preventive Maintenance of Cleaning Equipment – V 2.0

Posted on By

This Standard Operating Procedure (SOP) defines the process for performing preventive maintenance on cleaning equipment used in aerosol manufacturing. The objective is to ensure that all cleaning equipment, including washers, brushes, and other cleaning systems, are functioning optimally to maintain the cleanliness of machines and equipment. Regular preventive maintenance minimizes equipment downtime, ensures consistent cleaning performance, and helps maintain compliance with Good Manufacturing Practices (GMP).
Click to read the full article.

Aerosols V 2.0

Posts pagination

Previous 1 … 5 6 7 … 15 Next

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

Read SOPs in your Language:

 - 
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

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.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme