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

  November 22, 2013  
Global Compliance Trainings, 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.

Organized by: Global Compliance Trainings
Invited Speakers: Gregory P.Martin
Deadline for Abstracts: 2014-01-20
Registration: 2013-11-22
E-mail: globalcompliancetrainings1@gmail.com
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