Wednesday, May 6, 2015

Root Cause Analysis for Better Deviation Investigations - GMP Training

Root Cause Analysis for Better Deviation Investigations - A cGMP Training Course

A top reason why companies receive a 483 is a deficiency in the deviation investigation process. In our experience, most employees need deviation investigation training, and here's why:
  • Staff struggle to solve problems
  • Teams often fail to get results
  • The pharma and biotech sector repeatedly demonstrate difficulty in complying with FDA expectations for thorough deviation investigations.
In this SkillsPlus International Inc. hands-on workshop, employees learn the most effective tools to determine the real root cause of the problem. Attendees use actual plant deviations to practice the use of the tools. Allan Dewes, the lead instructor, has taught this course all over the world with exceptional results.

Call Allan (415) 948-5220, or learn more: http://www.skillsplusinc.com/root_cause.htm

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