Webinar Overview
With the USP recently rejecting recombinant Factor C (rFC) as a compendial endotoxin test, the technology has been receiving more attention in the media and our industry. Late 2019, we presented our initial LAL and recombinant study data from global pharmaceutical organizations’ water samples. After a careful analysis of the data, we conducted a second, larger study with hundreds of global water samples evaluating the ruggedness, repeatability, and specificity of commercially available recombinant Factor C products, as well as our own recombinant product in development, against a large panel of endotoxins.
View this webinar for a discussion of these new results and learn where recombinant products stacked up against LAL when it comes specificity and non-inferiority when testing relevant, real-world contaminated pharmaceutical water samples.
WEBINAR PRESENTER
Nicola Reid
Associate Director of Endotoxin Products
Charles River
We are providing digital education options to keep you learning about topics you may be interested in. For more information, visit criver.com/digital-education.
Charles River’s QC microbiology testing portfolio brings you modern products and services that deliver accurate, relevant, and reliable data to allow you to make confident decisions on your product quality and contamination control. Our unique combination of Endosafe® endotoxin testing, Celsis® rapid microbial detection, and Accugenix® microbial identification and strain typing keeps your manufacturing operations running efficiently and smoothly, lowers your cost to manufacture, and protects your reputation.
This post is related to:
Contamination Control: Quality Control, Lab Testing Services
