Precision in Practice: Sterisart®️ Manufacturing
Last Updated: May 2024
Overview
Sterility testing is a vital compendial requirement for final release, aimed at verifying that sterile products, including pharmaceuticals and medical devices, are free from viable microorganisms. This essential test determines the suitability of a manufactured batch for release.
To meet these standards, the equipment and tools used for sterility testing must be manufactured to the highest quality.
This video provides an overview of the manufacturing process for our Sterisart® Sterility Testing Canisters.
- Document type: Video
- Watch time: 2 minutes
Key Takeaways
- An overview of Sterisart® manufacturing - stepwise assembly to final packaging
- A glimpse at the integrity test performed on each canister as part of in-process controls
- The care and quality involved in manufacturing each sterility test system
This Resource is Designed for:
- Microbiological Testing Lab Managers
- Microbiology Managers for Pharma QC
- Sterility Testing Operators
- QC Analysts
- Method Validation Experts
Applications Supported:
- Sterility Testing
- Pharmaceutical Applications
- Microbiological Quality Control