Our global Endosafe® technical support laboratories operate in a shared network of expertise and experience dedicated to solving your endotoxin detection problems and increasing your laboratory efficiency. Wherever you need us, we can be a flexible, efficient, and cost-effective extension of your internal quality control laboratory.
In addition to order processing and price quotations within the United States, our Customer Service department can help you with product information and shipping details. Contact our Customer Service department at [email protected] or 1.800.762.7016.
Charles River Endosafe® products are also available internationally through a collection of distributors. For a list of worldwide locations, view our Partners page. To place an order from outside the United States, please contact us at [email protected].
|Software||Current Release Notes||Effective Date|
|Endosafe® EndoScan-V™ Endotoxin Measuring & Analysis Software 5.5.5 (SP3)||RNENDO-ESV555SP3-06||Nov 26, 2019|
|Endosafe® EndoScan-V™ Endotoxin Measuring & Analysis Software 6.0||RNENDOESV6-02||Dec 6, 2019|
|Charles River Cortex™ 1.1.2||RNENDO-COR112-02||May 21, 2019|
|Endosafe® nexgen-PTS™ and nexgen-MCS™||RNENDO-NEX1022-05||Dec 2, 2019|
|Endosafe® Nexus™ software version 2.6.0||RNENDO-NEXUS26-03||Aug 27, 2019|
|Endosafe® EndoScan-V™ Endotoxin Measuring & Analysis Software 6.0.1||RNENDO-ESV601-00||Dec 16, 2019|
Please contact your local representative for release notes and further information.
For further assistance on in-house troubleshooting, methods development, regulatory guidance, or other technical questions, please contact our technical support team at
Learn about our Endosafe®-PTS™ end-of-life policy and request information about upgrading to the Endosafe® nexgen-PTS™ (PTS150). Time to upgrade
Hints and Tips for Ensuring a Successful LAL Product Validation
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.