The Endotoxin Testing Blog
CMD blog posts is your source for guidance, regulatory insight, and practical strategies in endotoxin testing.
Whether you're working in pharma, biotech, diagnostics or medical devices, this blog is built for scientists, QA teams, and regulatory leads. Each post is authored by our team of scientific and regulatory specialists to help you make informed, compliant, and cost-effective decisions.
How to Validate an Endotoxin-Free Manufacturing Process
This blog outlines the validation process to demonstrate that a manufacturing facility or cleanroom consistently yields endotoxin-free outputs.
The Difference Between Endotoxin and Bioburden Testing
Ensuring the quality and purity of parenterally administered pharmaceutical drugs and medical devices is a key prerequisite for patient safety and for the generation of reliable and accurate laboratory results.
When and Why Do You Need Endotoxin Testing?
Endotoxins, which are strong pyrogens, are a component of the outer membrane of gram-negative bacteria. They are shed by gram-negative bacteria primarily during cell lysis and are widespread in the environment.