Lonza's Endotoxin Testing Service combines their expertise with full service reporting, offering both research and pharmaceutical customers’ routine and customized endotoxin testing.
Lonza’s Endotoxin Detection Testing laboratories are located in their cGMP-certified manufacturing plants in Walkersville, MD USA and in Verviers, Belgium. The Endotoxin Testing Service is designed for customers from the pharmaceutical industry, medical device companies, research and environmental laboratories.
Pharmaceutical-grade testing is offered both in the U.S. and Europe. This service includes all of the validation steps required during a product validation program and requested by regulatory authorities to be compliant with the current harmonized Bacterial Endotoxins Test (BET) as defined in the U.S. Pharmacopeia (USP) and European Pharmacopeia (EP). For the medical device industry, the service complies with the USP Monograph General Chapter, Citation <161> Transfusion and Infusion Assemblies and Similar Medical Devices.
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