THE CONTENT OF THIS WEBINAR IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT INTENDED TO CONVEY LEGAL OR OTHER PROFESSIONAL ADVICE.
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.
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