Standard Operating Procedure for Preservative Efficacy Testing in Gels
1) Purpose
The purpose of this SOP is to define procedures for testing the efficacy of preservatives in gel formulations to ensure the prevention of microbial growth over the product’s shelf life.
2) Scope
This SOP applies to all personnel involved in preservative efficacy testing of gel products within the pharmaceutical manufacturing facility.
3) Responsibilities
Quality Control (QC) Analyst: Perform preservative efficacy testing according to this SOP.
Microbiologists: Assist in testing and interpreting results.
Quality Assurance (QA) Team: Review and approve preservative efficacy testing procedures and results.
4) Procedure
4.1 Sample Preparation
4.1.1 Prepare samples according to specified guidelines to ensure representative analysis.
4.1.2 Ensure samples are stored under appropriate conditions before testing.
4.2 Inoculation of Samples
4.2.1 Inoculate gel samples with specified microorganisms according to regulatory guidelines.
4.2.2 Ensure uniform distribution of microorganisms within the samples.
4.3 Incubation
4.3.1 Incubate inoculated samples under controlled conditions for specified time periods.
4.3.2 Monitor and document the conditions throughout the incubation period.
4.4 Microbial Enumeration
4.4.1 Perform microbial counts at designated time intervals (e.g., 7, 14, 21, and 28 days).
4.4.2 Use validated methods such as plate counting or automated microbial detection systems.
4.5 Data Analysis
4.5.1 Analyze data to determine the reduction of microorganisms over time.
4.5.2 Compare results against acceptance criteria to assess preservative efficacy.
4.6 Reporting and Documentation
4.6.1 Document testing procedures, results, and analysis comprehensively.
4.6.2 Maintain detailed records of preservative efficacy testing for batch records and regulatory compliance.
5) Abbreviations, if any
SOP: Standard Operating Procedure
QC: Quality Control
QA: Quality Assurance
6) Documents, if any
– Preservative Efficacy Testing Records
– Method Validation Reports
– SOP for Sample Preparation and Handling
7) Reference, if any
– USP General Chapter <51> Antimicrobial Effectiveness Testing
– ICH Q1A(R2): Stability Testing of New Drug Substances and Products
– Company-specific preservative efficacy testing guidelines
8) SOP Version
Version 1.0
