This webinar examines a critical question facing today’s pharmaceutical quality control laboratories: Are endotoxin testing workflows still fit for purpose in today's laboratory? As testing volumes, compliance expectations, and operational pressures continue to evolve, many laboratories are reassessing traditional Bacterial Endotoxins Test (BET) workflows and exploring opportunities to improve efficiency, standardization, and performance.
Participants will explore why laboratories are rethinking BET today and how the publication of water monographs within USP <86> is creating new opportunities for change. The discussion will address key regulatory considerations, including confidence from agencies and compendia, as well as a practical, step-by-step approach to validation and implementation. Attendees will then learn what an optimized endotoxin testing workflow should look like, including an assessment of the hidden costs and operational burden associated with current processes. Finally, the webinar will demonstrate how GOPLATE™ can help modernize endotoxin testing workflows, delivering measurable operational efficiencies, workflow simplification, regulatory confidence, and tangible business value for the laboratory.
In this webinar you'll learn:
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