Updated April 26, 2018
You asked for it, so we delivered!
The most popular class with Allan Dewes, “Root Cause Analysis and Investigation Report Writing” is now available as an online self-study course. In 3-1/2 hours you’ll learn about the tools used to conduct a thorough deviation investigation. You’ll also learn great tips and get clear guidance on how to write a deviation investigation report. This class is not just theory and offers clear examples. Private email-based coaching is also available.
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Free GMP tip on root cause analysis (RCA)
The FDA says, “Human error is not a root cause.” If your first reflex is blaming human error, it’s time to re-think the situation in order to identify the real root cause of the human error.
There are several categories of human errors: slips, lapses, and induced errors. These can account for a large percentage of errors. In order to understand these human errors in more detail, they can be investigated through the use of investigative tools such as a Walk Through Analysis or Control Barrier Analysis.
Once the underlying contributing factors and real root cause(s) are understood, then they can be controlled (in many cases).
Learn more about this topic by taking these courses by SkillsPlus Intl Inc:
Root Cause Analysis for Better Investigations – A cGMP QSR GMP Training Course
Deviation Investigation Report Writing – A GMP QSR cGMP Training Workshop
You might also be interested in:
GMP Training – Live, onsite courses taught by SkillsPlus Intl Inc.
Go to www.GMPprof.com – Our GMP E-learning & Multimedia Resources website
Tags: cGMP, Compliance training, Corrective and preventive action, course, deviation, FDA, GMP, QSR, RCA, report, root cause analysis, training, workshop, writing