Procedure for Strip Pack Integrity Testing
1) Purpose
The purpose of this SOP is to outline the procedure for testing the integrity of strip packs used for packaging pharmaceutical products to ensure they meet quality and safety standards.
2) Scope
This SOP applies to all strip packs used for packaging pharmaceutical products, requiring testing to comply with regulatory requirements and internal specifications regarding packaging integrity.
3) Responsibilities
Quality Control (QC) Department: Responsible for performing strip pack integrity testing.
Quality Assurance (QA) Department: Responsible for review and approval of testing procedures and results.
Manufacturing Department: Responsible for providing strip packs and support during testing.
4) Procedure
4.1 Sample Selection:
4.1.1 Select representative strip packs from current production batches.
4.1.2 Ensure samples include different pack sizes and configurations.
4.2 Visual Inspection:
4.2.1 Inspect each strip pack visually for defects such as punctures, tears, or incomplete seals.
4.2.2 Document observations and categorize defects according to predefined criteria.
4.3 Seal Integrity Testing:
4.3.1 Perform seal integrity testing using appropriate methods (e.g., dye penetration, burst strength, vacuum decay).
4.3.2 Conduct testing under controlled conditions and record test parameters and results accurately.
4.4 Peelability Testing: 4.5 Compatibility Testing: 4.6 Data Analysis: 4.7 Reporting: QC: Quality Control Strip Pack Integrity Testing Report USP Chapter 1216 – Pharmaceutical Dosage Forms: Tablet and Capsule Dissolution Testing Version 1.0
4.4.1 Evaluate the ease and consistency of strip pack opening to ensure product protection and user convenience.
4.5.1 Verify compatibility of strip pack materials with pharmaceutical products to prevent interaction or degradation.
4.5.2 Perform testing under simulated storage conditions (e.g., temperature, humidity).
4.6.1 Compile and analyze test data, including visual inspection results, seal integrity tests, peelability testing, and compatibility assessments.
4.6.2 Review data against acceptance criteria and regulatory standards.
4.7.1 Prepare a Strip Pack Integrity Testing Report summarizing test procedures, results, and conclusions.
4.7.2 Include recommendations for improvements or corrective actions based on test findings.
4.7.3 Submit the report to QA for review and approval and maintain records as per facility procedures.5) Abbreviations, if any
QA: Quality Assurance6) Documents, if any
Visual Inspection Records
Seal Integrity Testing Data
Peelability Testing Results7) Reference, if any
FDA Guidance for Industry – Container Closure Systems for Packaging Human Drugs and Biologics8) SOP Version
