The essential guide to modernise your bacterial
Reliability and compliance for modern endotoxin testing
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.
This Essential BET Guide has been created by Sievers experts to help laboratories modernise their endotoxin testing strategy with practical advice, regulatory insights and proven automation solutions.
What will you learn inside?
- Key endotoxin testing improvements: reduce retests, gain efficiency, ensure sustainability, and compliance
- Practical steps to reduce assay time and human error
- Sustainable BET practices: minimising LAL reagent use and improving efficiency
- Side-by-side comparison of endotoxin methods and testing systems
- How automation ensures compliance with USP <85>, EP 2.6.14, and JP 4.01
- Case insights on transitioning from manual to automated testing
Who should read this guide?
- QC Managers and Lab Directors seeking to improve efficiency, reduce retests, and ensure data integrity
- Microbiologists and Lab Technicians looking to optimise assay setup and reduce testing time
- QA and Regulatory Specialists ensuring compliance with GMP, 21 CFR Part 11, SOPs, and validation

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