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SOP for Establishing Shelf Life Using Stability Data

Procedure for Determining Shelf Life of Pharmaceuticals Using Stability Data

1) Purpose

The purpose of this SOP is to provide guidelines for establishing the shelf life of pharmaceutical products using data obtained from stability studies.

2) Scope

This SOP applies to all stability studies conducted to determine the shelf life of pharmaceutical products. It is relevant for personnel in the quality control, research and development, and regulatory affairs departments.

3) Responsibilities

The responsibilities for establishing shelf life using stability data are as follows:

Quality Control Team: To provide stability data for analysis and shelf life determination.
R&D Team: To

analyze data and determine the appropriate shelf life.

Regulatory Affairs Team: To ensure compliance with regulatory guidelines for shelf life determination.

Stability Study Coordinator: To oversee the data collection, analysis, and reporting process.

4) Procedure

The detailed stepwise procedure for establishing shelf life

using stability data is outlined below:

Data Collection and Review:

4.1 Collect all stability data obtained from long-term, accelerated, and intermediate studies.
4.2 Review data for completeness and accuracy.
4.3 Identify critical quality attributes (CQAs) that may affect the shelf life.

Data Analysis:

4.4 Analyze the data to identify trends and calculate degradation rates.
4.5 Use statistical tools to determine the shelf life based on the degradation rate and predefined criteria.
4.6 Compare the data against regulatory requirements to ensure compliance.

Determination of Shelf Life:

4.7 Establish the shelf life based on the stability data and analysis results.
4.8 Confirm the shelf life by considering any additional factors such as packaging and storage conditions.

Documentation and Reporting:

4.9 Document the shelf life determination process and results in a comprehensive report.
4.10 Review and approve the report by relevant stakeholders.
4.11 Submit the report to regulatory authorities as required.

Review and Update:

4.12 Regularly review the shelf life based on new data or regulatory updates.
4.13 Update the shelf life information as needed.

5) Abbreviations, if any

CQA: Critical Quality Attribute
ICH: International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use

6) Documents, if any

Shelf Life Determination Report
Stability Data Sheets
Regulatory Compliance Checklists

7) Reference, if any

ICH Q1E: Evaluation for Stability Data

8) SOP Version

Version 1.0