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CAPA Practices for FDA Regulated Industry: Practical Tips to Meet FDA's Expectations
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CAPA Practices for FDA Regulated Industry: Practical Tips to Meet FDA's Expectations

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Do you know that FDA inspectors are trained to look for 20 specific items in 3 broad areas specific to Corrective and Preventive Actions (CAPA) during an audit? More often than not FDA 483s and …

Do you know that FDA inspectors are trained to look for 20 specific items in 3 broad areas specific to Corrective and Preventive Actions (CAPA) during an audit? More often than not FDA 483s and Warning Letters list inadequate CAPA practices as one of the major findings.

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http://www.audioeducator.com/pharma-biotech/capa-practices-10-17-13.html

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  • 1. For more information:- http://www.audioeducator.com/pharma-biotech/capa-practices-10-17-13.html For more information:- http://www.audioeducator.com/pharma-biotech/capa-practices-10-17-13.html
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