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.
Using Root Cause Analysis and CAPA for Conducting Effective Investigations of Atypical and Out of Specification Laboratory Results
30 May 2014, michigan., United States
Introduction
Venue
online
online, 201,N Squirrel road,, Auburn Hills,, Suite 1007,, michigan., 48326., United States
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Organised by
Global Compliance Trainings
Contact information
Mr john gordan
201,N Squirrel road, Suite 1007, Auburn Hills, Suite 1007,, Auburn Hills,, michigan., 48326, United States of America
2482120588
Contact us by email
201,N Squirrel road, Suite 1007, Auburn Hills, Suite 1007,, Auburn Hills,, michigan., 48326, United States of America
2482120588
Contact us by email
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