USP Reference Standard Endotoxin, RSE (ES-0526-YC146)

Product Overview

During pharmaceutical manufacturing, biologics processing and medical device validation, there is zero margin for error in pyrogen testing. The LAL bacterial endotoxins test is highly sensitive and the quantitative data must be anchored to an indisputable and globally recognized benchmark.
The USP Reference Standard Endotoxin (RSE) is the definitive primary standard used to calibrate testing systems worldwide. The USP RSE serves as the master baseline against which all secondary standards (e.g., Control Standard Endotoxin (CSE)) are qualified. The RSE is a prerequisite for primary assay validation, instrument qualification and regulatory audit compliance. Sourced with high precision and certified under stringent international criteria, it ensures assay data stands up to global regulatory scrutiny.

Applications

As standards for endotoxin testing

Endotoxin Level

10000 EU (USP)

Package

1 vials

Storage

Store at 4°C.