The essential guide to modernise 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 Efficient 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?

Endotoxin testing improvements and how they 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, and JP 4.01
Case insights on transitioning from manual to automated testing
Sustainable BET practices: minimising LAL reagent use and improving efficiency

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, Lab Technicians, or lab techs looking to optimise assay setup and reduce testing time