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A Standard Procedure For Quality Assurance Deviation Management What is a Deviation: A Deviation is a departure from standard procedures or specifications resulting in non-conforming material and/or processes or where there have been unusual or unexplained events which have the potential to impact on product quality, system integrity or personal safety. For compliance to GMP and the sake of continuous improvement, these deviations are recorded in the form of Deviation Report (DR). [VIEW ARTICLE]Comments RSS Feed For This Article: 
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Subject: Manage Reported Deviation
This is a very interesting article. But, in my opinion, the "How to Manage Reported Deviation" section should contain more information.. It's a crucial part!
Thanks!