2min chapter

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Most Common Problems Found During FDA Inspections in 2022

Global Medical Device Podcast powered by Greenlight Guru

CHAPTER

CAPA Design Controls - Root Cause Analysis

A lot of the reasons you go again is not establishing the documentation or not performing, whether it's risk analysis and connecting those things. I wonder sometimes, well, with CAPA particularly how much of industry truly knows how to do root cause analysis. A lot of people talk about the root cause of the problem but rarely, rarely. Do I see anybody get anywhere remotely close to the actual to real root cause they're oftentimes dancing around the surface. And so in my opinion, and again,. I know this is going to sound harsh to some people. I think what is the rootCause of many if not most of the problems that we run into isn't up here. It's between

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