Webinar Overview

The newest USP chapter on endotoxin testing fills in the regulatory gaps that have resulted following the withdrawal of the 1987 FDA Guideline and implementation of its replacement Q&A. In this webinar, we analyze the most important points introduced by this guideline and their potential impact on our daily lab work. Join us as we discuss:

  • Preparatory requirements on RSE/CSE, consumables, analyst qualification, calibration, and the laboratory environment
  • Method suitability for endotoxin limits, MVD, suitability testing, and common test interferences
  • Routine testing for sampling, pooling, out of specification results, and retesting considerations and standard curve control
  • Alternate test methods


Webinar Presenter

Ben Fischer Headshot

Ben Fischer
Technical Service Specialist
Charles River


During this time of uncertainty, we are focused on providing digital education options to keep you learning about topics you may be interested in. For more information, visit criver.com/digital-education.