What has your experience with endotoxin systems and product validation been like? In this webinar, we will look at what steps are needed for a new platform to be considered fully validated, and we’ll dive into some of the challenges that the typical Quality Control lab may experience.

Then, we'll discuss what the optimal validation process looks like and how an organization can save time and resources using the Sievers Eclipse BET Platform. Finally, we’ll explain how the platform simplifies and streamlines validation of product samples and wrap up by showcasing some of the software’s most convenient features. Getting a validated, automated system deployed has never been so easy.

In this webinar, you will learn why endotoxin product validation has traditionally been challenging and how a new bacterial endotoxins testing platform can eliminate some common complexities. You’ll also learn about the requirements for a fully validated system, and what the ideal validation scenario looks like.

Who should attend:

• QC Analysts
• QC Managers
• QC supervisors
• Metrology
• Validation engineers