LCMS webinars focusing on LC/MS - page 60

Throughout this session, we will examine essential facets of manufacturing, the critical role of USP standards in guaranteeing quality, and optimized workflows designed for thorough quality assessment.

In this webinar we will outline the main factors that can influence proteomic and more generally, mass spectrometry quantitation and provide advice on how to prevent potential quantitation biases.

Different Perspectives and Strategies for Liquid Chromatography Peak Capacity Optimization and Method Development.

Discover how direct analysis in real time (DART), with high-resolution mass spectrometry (HRMS), allows the generation of reliable analytical results faster and easier than alternative techniques.

In this webinar we present an enhancement to the well-established two-tier testing strategy which not only addresses fraud but also other key attributes such as quality, potency, and purity.

Learn how a quantitative shotgun lipidomics solution is used for establishing a lipidomics atlas, and mapping cell and disease-specific lipid changes.

The objective of this work is to develop an efficient method for the untargeted characterization of various açaí extracts.

This presentation will detail the development of two new Total Organic Fluorine methods that use combustion-ion chromatography to more comprehensively capture PFAS, capturing known and unknown organic fluorine.

We will focus on trends in analytical workflows in pharma from drug discovery and development right through to quality control of manufactured drugs, that help pharma labs succeed in these challenges.

This webinar shows tips to setting up nSEC-MS on BioAccord LC-MS, data generated and lessons learned from case studies, and method optimization and options do consider depending on your analytical needs.