+1 (800) 638-8174
+1 (800) 521-0390
+ 32 87 321 611
+ 32 87 321 611
Contact your local Lonza Distributor
Tel: +1 (800) 638-8174
Fax: +1 301 845 8291
Listen to Allen Burgenson, Lonza's Regulatory Affairs Manager, review the FDA’s latest guidance on Pyrogen and Endotoxin Testing
Endotoxin Detection is a part of Lonza BioScience’s QC Testing and Analytical Services that offers a comprehensive QC platform.
Endotoxin Detection Expertise
Lonza has been providing endotoxin detection products and services for nearly 40 years, leading the way in innovation for products, methods and software.
In the 1980s, Lonza developed and commercialized the first FDA licensed endpoint quantitative LAL assay, QCL-1000™ Endpoint Chromogenic LAL Assay. We continued to improve upon the quantitative technologies by launching the Kinetic-QCL™ LAL Assay, the kinetic chromogenic LAL method that revolutionized endotoxin detection testing.
In 2003, Lonza brought to market an endotoxin detection method that does not rely on the use of horseshoe crab blood as the raw material. The PyroGene™ assay uses a recombinant form of Factor C (rFC), the endotoxin-sensitive protein that initiates the LAL clotting cascade. The recombinant technology is endotoxin-specific, eliminating false-positive glucan reactions. It offers exceptional performance and reliable, lot-to-lot consistency, compared to biologically based products, while reducing the dependency on the horseshoe crab. In 2009, 510(K) submissions were FDA-approved using PyroGene™ rFC as a final release test.
Welcome to the Evolution
Recognizing the importance that software plays in accurate analysis and reporting, Lonza has made significant investments in software and has its own in-house development systems and programmers, dedicated to producing robust endotoxin detection software.
WinKQCL™ Software is Lonza’s industry leading endotoxin detection and analysis software offering a fully-integrated solution for quantitative endotoxin detection testing, data management and reporting needs. WinKQCL™ Software meets 21 CFR Part 11 technical requirements for electronic records and signatures, audit trails and database archiving.
Endotoxin Testing Services
Our Endotoxin Testing Services (U.S. and Europe) are designed for customers from the pharmaceutical industry, medical device companies, research and environmental laboratories.
Our laboratories in Walkersville, Maryland and Verviers, Belgium, are located in cGMP-certified manufacturing plants, providing a high level of expertise in methods for endotoxin testing.
USP and EP Compliant
Pharmaceutical-grade testing 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, our service complies with the USP Monograph General Chapter, Citation <161> Transfusion and Infusion Assemblies and Similar Medical Devices.
As a primary manufacturer of LAL, we offer a wide range of endotoxin testing solutions to fit your requirements. From the simplicity of gel clot testing to the productivity of fully robotic systems, Lonza covers the LAL evolutionary scale.