Waters recently partnered with United States Pharmacopeia (USP) experts to host a webinar discussing the upcoming changes in the pending USP General Chapter on chromatography that will provide increased flexibility for gradient methods. Here’s an extended Q&A from the webinar.
Q&A from a recent forensic toxicology webinar on using an ACQUITY UPLC I-Class/Xevo TQ-S micro MS system for quantifying cannabinoids in oral fluid.
The development of chromatographic methods for natural products is challenging due to the complexity of the sample matrix and analyte chemistry. However, by understanding the fundamental parameters of your chromatography and strategies for efficient detection,… Read more >
On Wednesday evening after dinner and my usual digestif, I was watching the webcast “Making Ion Mobility Mass Spectrometry Routine” when my son walked by. “Wow dad, that’s kind of cool! What the heck is… Read more >
Are you being asked to reduce laboratory costs and increase laboratory efficiency while ensuring your data meets regulatory expectations? The amount of data being produced by your chromatography data system (CDS) increases every year. Being… Read more >
There is increased concern regarding the authenticity of basmati rice throughout the world. For years, traders have been passing off a lesser quality rice as the world’s finest long-grained, aromatic rice, basmati, in key markets like… Read more >
Empower® 3 Method Validation Manager (MVM) allows you to perform chromatographic method validation, from protocol planning through final reporting, in one application. Recently, we sponsored a webinar showing ways you can streamline your workflow throughout… Read more >
Webinar: QbD Development of a Purity Method Chromicent GmbH (Berlin, Germany) managing directors Alexander Schmidt and Mijo Stanic are experts in the development and validation of analytical methods according to the latest quality-by-design approaches. The… Read more >