Webinar Overview

A critical component to ensuring a treatment or medical device is safe for use is the Bacterial Endotoxins Test (BET). Compendial BET methods include the gel-clot and kinetic LAL test, but their accuracy can only be as good as the validation performed on them.

Whether you’re new to endotoxin product validations or just need a refresher, this webinar will provide you with information on the steps necessary for LAL product validation, how they’re different for gel-clot and kinetic methods, and product validation examples following guidance from the USP and EP.


Webinar Presenter

Hayden Skalski headshot

Hayden Skalski, BS
Endosafe® Technology and Market Development Manager, 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.