On-Demand Webinar:Elemental Impurities - A Deep Dive into Potential Contamination Sources

With less than six months until the retirement of the methods outlined in USP General Chapter <231> on January 1, 2018, there’s still plenty to discuss regarding this regulatory change. An often overlooked scenario when testing for elemental impurities is the possible contamination from everyday pharmaceutical machinery. It’s important to understand and implement policies that can assist in a successful right-first-time risk assessment that accurately reflects your process.

This webinar will address:

  • What has changed since our last webinar, Elemental Impurities- Everything you Need to Know
    • The change to USP <232>, effective August 1, 2017
  • An overview of the upcoming regulatory change and what it means for you
  • Possible contamination sources that could affect the results of your elemental impurities analysis
  • Elemental impurity evaluation on container closure systems (USP <661>) and packaging components (USP <670>)

Length: 60 Minutes



Chris Williams, Manager






Ashley Taylor, Senior Scientist

Download On-Demand Webinar