20-Oct-2020 15:30 - 16:00 Europe/Berlin (UTC+01:00) English

Using ED-XRF for Screening of Pharmaceutical Products for Elemental Impurities According to ICH Q3D

The production of pharmaceutical products requires the analysis of a series of trace elements. Maximum concentration limits can be found in the ICH Q3D guideline. During the webinar the calibration and validation of an ED-XRF spectrometer for the screening of class 1 and class 2A elements as listed in ICH Q3D will be discussed. Aspects of installation qualification (IQ) and operational qualification (OQ) will be covered.