Skip to main content
  • On-demand 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.

View our on-demand 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:

  • 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

Speaker: David Peterson, senior advisor and subject matter expert at UL

Watch the on-demand webinar

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

Get in touch

Have questions, need specifics? Let's get this conversation started.

Help and support

How can we help?