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

SOP for Storage Conditions of Aerosols

Posted on By

SOP for Storage Conditions of Aerosols

Standard Operating Procedure for Storage Conditions of Aerosol Products

1) Purpose

The purpose of this SOP is to establish guidelines for the proper storage of aerosol products in the pharmaceutical industry. This ensures product stability, integrity, and compliance with regulatory requirements during storage.

2) Scope

This SOP applies to the warehouse and storage areas at [Company Name], responsible for storing aerosol products according to specified conditions and guidelines.

3) Responsibilities

Warehouse Manager: Oversees storage operations and ensures adherence to SOP.
Quality Assurance (QA) Personnel: Monitor storage conditions and conduct periodic checks.
Production Personnel: Ensure proper labeling and segregation of products.

See also  SOP for Cleaning Validation in Aerosol Production

4) Procedure

4.1 Storage Conditions:
4.1.1 Store aerosol products in designated storage areas with controlled temperature and humidity.
4.1.2 Ensure storage areas are clean, dry, and free from contaminants.

4.2 Labeling and Identification:
4.2.1 Label each stored batch with product details, batch number, and expiry date.
4.2.2 Maintain clear identification and segregation of different products.

4.3 Handling Procedures:
4.3.1 Handle aerosol products with care to prevent damage or leakage.
4.3.2 Follow procedures for handling hazardous materials if applicable.

4.4 Storage Monitoring:
4.4.1 Monitor storage conditions regularly using calibrated equipment (e.g., temperature loggers).
4.4.2 Record temperature and humidity data as per defined frequencies.

See also  SOP for Regulatory Submission for Aerosols

4.5 Security and Access Control:

/> 4.5.1 Implement security measures to prevent unauthorized access to storage areas.
4.5.2 Restrict access to authorized personnel only.

4.6 Documentation:
4.6.1 Maintain records of storage conditions, including monitoring logs and temperature excursions.
4.6.2 Document any deviations from specified storage conditions and corrective actions taken.

5) Abbreviations, if any

SOP: Standard Operating Procedure
QA: Quality Assurance

6) Documents, if any

Storage Monitoring Logs
Temperature and Humidity Records
Batch Manufacturing Record (BMR)

7) Reference, if any

ICH Q1A: Stability Testing Guidelines
FDA Guidelines on Good Storage Practices

8) SOP Version

Version 1.0

See also  SOP for Evaluation of Propellant Leakage in Aerosols
Aerosols Tags:Aerosol batch manufacturing, Aerosol change control procedures, Aerosol cleaning validation, Aerosol contamination prevention, Aerosol documentation requirements, Aerosol equipment calibration, Aerosol equipment cleaning, Aerosol final product inspection, Aerosol formulation development, Aerosol in-process testing, Aerosol manufacturing process, Aerosol method development, Aerosol microbial testing, Aerosol packaging guidelines, Aerosol particle size analysis, Aerosol personnel training, Aerosol process validation, Aerosol production SOP, Aerosol quality control, Aerosol raw material inspection, Aerosol stability testing, Aerosol stability testing methods, Aerosol sterility maintenance, Aerosol storage conditions, Aerosol waste disposal procedures

Post navigation

Previous Post: SOP for Quality Control Testing of IV Injections
Next Post: SOP for Waste Management and Disposal

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

Go to mobile version