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Using Root Cause Analysis & CAPA for Conducting Effective Investigations of Atypical & Out of Specification Laboratory Results

Posted on Aug 23, 2014 3:16:00 AM

 

Webinar - Online

This webinar focuses on the use of Root Cause Analysis, Corrective and Preventive Action to address the investigation of Out of Specification (OOS) or atypical results, in the context of the procedures recommended by the FDA OOS Investigation Guidance, to complete investigations more quickly and effectively.Using this approach will decrease the likelihood that investigations for the same root cause will occur.

Speaker: Gregory P. Martin

Organization: Global Compliance Trainings

For more information, please visit: http://www.globalcompliancetrainings.com/index.php?rout...

May 25, 2014 (10:00 AM - 01:00 PM) Recorded Webinar

201,N Squirrel road, Suite 1007, Auburn Hills, Michigan United States - 48326

 Contact: John Gordan (webinar@globalcompliancetrainings.com)

Phone: 2482120588

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Tags: 2014, Michigan, United States, Webinar, May, Quality Control, Life Sciences, Conference, MI, laboratory

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