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