Standard Operating Procedure for Microbial Testing in Granules

1) Purpose

The purpose of this SOP is to outline the procedure for conducting microbial testing on granule formulations in the pharmaceutical industry to ensure compliance with microbiological quality standards.

2) Scope

This SOP applies to all personnel involved in the microbial testing of granule formulations within the pharmaceutical quality control (QC) department.

3) Responsibilities

Microbiology Analyst: Responsible for performing microbial testing and documenting results.
Quality Assurance (QA) Department: Responsible for reviewing and approving the microbial testing procedure and results.

4) Procedure

1. Sample Collection:
   1. Collect representative samples of the granule formulation as per sampling plan.
   2. Follow aseptic techniques during sample collection to avoid contamination.
2. Sample Preparation:
   1. If necessary, prepare the sample for testing (e.g., dilution) according to specified procedures.
   2. Ensure that sample preparation does not compromise the integrity of microbial analysis.
3. Testing Method:
   1. Perform microbial testing using appropriate methods such as membrane filtration or plate count techniques.
   2. Incubate samples under suitable conditions to promote microbial growth.
4. Data Collection:
   1. Record all relevant details including sample identification, testing dates, and incubation conditions.
   2. Document any deviations or incidents encountered during testing.
5. Interpretation of Results:
   1. Interpret test results based on established acceptance criteria for microbial limits.
   2. Evaluate the presence of objectionable microorganisms that could pose a risk to product safety.
6. Reporting:
   1. Prepare a microbial testing