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UL to Host Webinar on QRM and FMEA in the Pharmaceutical Industry


UL will hold a webinar on Thursday, October 28, at 1:00 p.m. ET, on quality risk management (QRM) in the pharmaceutical industry.

David Peterson, senior advisor and SME at UL, will lead the discussion with topics including:

  • The definition and principles of QRM in the pharmaceutical industry
  • Basic steps of a typical QRM process
  • Process analysis tools – specifically, the failure mode and effects analysis (FMEA)
  • Why FMEA is important in evaluating risk

Registration for “Applying FMEA in the Pharmaceutical Industry” is free. See UL’s website to learn more and register.

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