The essential guide to modernize your bacterial endotoxin testing
Achieve reliability and compliance for modern BET
Bacterial endotoxin testing (BET) plays a vital role in ensuring the safety of pharmaceuticals, medical devices and water-for-injection systems. Yet many laboratories still face operational challenges, from time-consuming manual processes to data integrity risks and resource constraints.
The Streamlined Endotoxin Testing Guide has been created by Sievers experts to help laboratories reduce retest rates and improve endotoxin testing reliability.
What will you learn?
- Endotoxin testing improvements - how to reduce retests, gain efficiency, and ensure sustainability
- Practical steps to reduce assay time and risk from human error
- Side-by-side comparison of endotoxin methods and testing platforms
- How automation ensures compliance with USP <85>, EP 2.6.14, JP 4.01, and ChP 1143
- Case studies on transitioning from manual to automated testing
- Sustainable BET practices: minimizing LAL reagent use and transitioning to recombinant reagents
Who should read this guide?
- QC Managers, Lab Directors, or anyone seeking to improve efficiency, reduce retests, and ensure data integrity
- QA Managers and Regulatory Specialists who develop SOPs, oversee validation with an eye for compliance with GMP and 21 CFR Part 11
- Microbiologists or Lab Technicians seeking to optimize assay setup and reduce testing time