Learn how to readily perform high-speed analysis of linezolid following the draft guidance of International Harmonization of Pharmacopoeias.
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Learn how to confirm the identity of related impurities and a genotoxic impurity in a drug substance using a single quadrupole mass detector.
This application note will help you understand how trap-free 2D LC-MS allows online conversion of non-volatile to volatile mobile phase conditions.
The aim was to develop a rapid, cost-effective, modified USP <467> HS-GC-FID method for residual solvent determination in pharmaceutical products
Discover a method for the determination of genotoxic nitrosamines in Valsartan according to Chinese Pharmacopoeia and US FDA recommended methodology.
Pharmaceutical impurity method development to a complete HPLC workflow comprising multiple detectors, to strategies to improve productivity & reduce cost.
Discover the vital role of compendial methods in pharmaceutical analysis and how to make adjustments to them for HPLC separations
Here the analysis of irbesartan and amlodipine besilate was performed using Nexera™-i MT with results showing the reliable transfer of the listed analytical conditions for these two...
To better prepare QA/QC lab analysts and technicians for digitalisation, Singapore Polytechnic’s (SP) School of Chemical and Life Sciences (CLS) and Shimadzu, have set up a Scalable,...
This compendium provides detailed methods for the analysis of trace elements in pharmaceutical products using AAS, ICP-OES and ICP-MS covered by the NEW USP chapters 232 and...
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