The introduction of USP<232> and ICH Q3D requires the pharmaceutical industry to re-evaluate how elemental impurity (heavy metal) testing is performed.
ICP-MS is often used for this type of analysis, but requires a high level of user expertise and can be time-consuming. USP <735> and EP 2.2.37 enables the use of X-ray fluorescence (XRF) spectrometry as an alternative technology for pharmaceutical elemental impurity testing.
In this webinar, the capabilities of the Epsilon 4 benchtop system set up with our unique calibration solution to analyze elemental impurities according to current regulatory requirements, will be demonstrated.
The webinar will take place on 6 December from 10:30-11:30 (GMT-5:00). Speakers Dr Lieven Kempenaers and Dr Michel Zoontjes will demonstrate how simple and quick XRF is to use for users of all levels of experience, especially with the newly launched calibration solution. There will be a live sample preparation and measurement demonstration taking place during the presentation.
Click here to register for the event.