Making the Right Choices in SEC Method Development
Size exclusion chromatography (SEC) is the method of choice for the quantification of aggregates in biotherapeutic samples. Proteins undergo aggregation for a variety of reasons, particularly when exposed to stress conditions such as changing concentration, pH or temperature. It is important to consider these factors when using SEC for quantifying aggregates. We will provide you with practical hints and tips which will help you design optimum methods, select the correct column, and choose the right buffer solution for your analyses. This webcast will be your complete SEC development toolkit.



Demystifying Software Validation: What is It Really and When Do I Need to Do It
The term “software validation” can trigger many responses, including dread and confusion. What is the difference between qualification and validation? What systems need to be validated? When do systems need to be revalidated? How much validation work is enough? In addition to answering these questions, this webinar will provide a foundation for thinking critically (and correctly) about system definitions, software validation, including discussions on the differences between qualification and validation, risk-based validation, and revalidation. You’ll learn from Loren Smith, Agilent’s software compliance expert and a University of California Berkeley instructor with nearly three decades of regulated software experience.

Automated LC Method Development - Fundamentals and Columns
From fundamentals to latest advancements: this three-part webinar series gives you a comprehensive overview to automated method development for liquid chromatography (LC). We will use the Agilent InfinityLab LC Method Development Solution to demonstrate how you can develop methods faster and with maximum efficiency.