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