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Oct 28, 2021
  • Webinar

Applying FMEA in the Pharmaceutical Industry

Gain insights into the principles of quality risk management (QRM) in the pharmaceutical industry and the basic steps of a typical QRM process.

A doctor operates a computer in a laboratory setting.

Date & Time

Starts

Oct 28, 2021 1:00pm EDT

Ends

2:00pm EDT

Location

Online

Join UL on Thursday, Oct. 28, 2021, for a webinar with David Peterson, senior advisor and SME at UL, as he introduces the definition and principles of quality risk management (QRM) in the pharmaceutical industry and outlines the basic steps of a typical QRM process.

Key takeaways from this webinar include:

  • QRM definition and principles
  • Process analysis tools, specifically, the failure mode and effects analysis (FMEA)
  • Why FMEA is important in evaluating risk:
    • Proactivity vs. reactivity
    • What causes failures
    • Effects of failures
    • Remediation of failures

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