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SOP for Stability Testing of Aerosols

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SOP for Stability Testing of Aerosols

Standard Operating Procedure for Stability Testing of Aerosol Products

1) Purpose

The purpose of this SOP is to establish guidelines and procedures for conducting stability testing of aerosol products in the pharmaceutical industry. This ensures that the products maintain their quality, efficacy, and safety over their intended shelf-life.

2) Scope

This SOP applies to the Quality Control (QC) department at [Company Name], responsible for conducting stability testing on aerosol products according to regulatory requirements and company standards.

3) Responsibilities

QC Manager: Oversees stability testing procedures and ensures compliance with SOP.
Stability Analysts: Perform stability testing and monitor product stability over time.
Quality Assurance (QA) Personnel: Review stability data and ensure adherence to regulatory guidelines.

See also  SOP for Conducting Process Validation for Aerosols

4) Procedure

4.1 Stability Study Protocol:
4.1.1 Develop a stability study protocol outlining testing conditions and parameters.
4.1.2 Define sampling points and storage conditions (e.g., temperature, humidity).

4.2 Sample Preparation:
4.2.1 Collect representative samples from each batch of aerosol products.
4.2.2 Ensure samples are stored in appropriate containers and labeled with batch details.

4.3 Testing Conditions:
4.3.1 Place samples in stability chambers set to specified conditions (e.g., accelerated, long-term stability).
4.3.2 Monitor samples at defined intervals for physical, chemical, and microbial stability.

4.4 Stability Testing:
4.4.1 Conduct tests such as appearance, pH,

active ingredient content, and propellant content.
4.4.2 Perform microbiological testing to assess microbial growth over time.

See also  SOP for Visual Inspection of Aerosols

4.5 Data Analysis and Reporting:
4.5.1 Record all stability test results accurately in stability study records.
4.5.2 Analyze data to determine product stability trends and shelf-life estimation.

4.6 Deviations and OOS:
4.6.1 Document any deviations from protocol or out-of-specification (OOS) results.
4.6.2 Investigate and report deviations to ensure corrective actions are implemented.

5) Abbreviations, if any

SOP: Standard Operating Procedure
QC: Quality Control
OOS: Out of Specification

6) Documents, if any

Stability Study Protocol
Stability Study Records
Batch Manufacturing Record (BMR)

7) Reference, if any

ICH Guidelines for Stability Testing
FDA Guidance for Industry: Stability Testing of Drug Substances and Products

See also  Aerosols: SOP for Out of Specification (OOS) Handling in Aerosol Production

8) SOP Version

Version 1.0

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

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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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