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This e-book shows how you can establish an effective CAPA system, which interfaces there are to other systems and what content a CAPA SOP should have.
1st edition 2015
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Excerpt from the GMP Compliance Adviser Inadequate CAPA procedures continue to be among the leading findings in U.S. FDA and European GMP inspections. During the implementation of a CAPA system it should be ensured that the CAPA system is understood as an important element of the pharmaceutical quality system and, consequently, that it is implemented uniformly company-wide or group-wide, as a governing system. How to Manage Corrective and Preventive Actions (CAPA) in a GMP Environment is the ultimate guide on building and implementing an effective CAPA compliance program. The e-book shows how you can establish an effective CAPA system, which interfaces there are to other systems and what content a CAPA SOP should have. Here’s an overview of what you’ll discover in its pages:
Reading Sample "How to Manage Corrective and Preventive Actions (CAPA) in GMP Environment"
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