LCMS webinars focusing on Academy/Principles - page 2

Join the Biopharma Fundamentals masterclass to learn practical LC-MS strategies for protein identity, purity, sequence, and PTM characterization in biopharmaceutical workflows.

This webinar will cover the guidelines defined in <621> and provide practical examples of how to apply them.

Discover why LC method transfer between legacy and modern systems is challenging. Learn which hidden parameters affect retention, peak shape, and robustness—and how to achieve reliable results.

Learn how to set up HRMS screening for success. Explore instrument capabilities, software tools, validation strategies, and workflow design to achieve reliable, unbiased LC/QTOF screening results.

Demystify high-resolution LC/MS screening. Learn how to design reliable HRMS workflows, avoid false results, and unlock the full potential of LC/QTOF screening for complex analytical applications.

Join us to learn about the best practices upon opening your new LC Column, how to clean and regenerate, and additional products and practices that can be used to minimize contamination getting onto LC columns!

Session 1 introduces accurate mass fundamentals, explaining why mass accuracy and resolution matter, what nominal mass can miss, and how accurate mass improves data interpretation and confidence.

Join USP and Waters experts to learn how to navigate regulatory updates, track open comment periods and Calls-for-Data, and understand how consumable and hardware inertness impacts analytical reliability.

Take a deep dive into typical mobile phase compositions; pH, buffers, organic solvents and other additives.

End-to-end Sequence Mapping and CQA Monitoring Workflows. LNP Characterization and Monitoring.