Webinar Overview
Long incubation periods and subjective visual assessments have long hampered the efficiency and accuracy of bioburden and sterility, yet these quality control assays are essential to ensure the safety of sterile compounded drugs. As manufacturers of these products, how do we keep patients safe and shelves stocked?
In this webinar, Dr. Wayne DeHaven of Pharmetric Laboratory discusses how amplified adenosine triphosphate (ATP) technology overcomes the limitations of these traditional test methods, eliminating days of sample incubation time while preserving current test protocols and delivering accurate contamination results.
Learn more about:
• Current challenges with traditional quality control assays for microbiology laboratories and manufacturers of sterile compounding drugs
• The distinct benefits of adopting rapid microbial detection test methods to provide compounders with faster and more confident results
• How a contract microbiology testing laboratory can easily switch to these rapid methods for your samples, extending these benefits to you
WEBINAR PRESENTER
Wayne DeHaven, PhD
Director of Quality
Pharmetric Laboratory
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.
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:
Quality Control/Analytical Testing
