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From GlobalCompliancePanel
CAPA Failure Investigation and Root Cause Analysis to Meet FDA Expectations - Webinar By GlobalCompliancePanel
Defined Failure Investigation and Root Cause Analysis is a major tool in product complaint, non-conformance, and OOS failure investigations, and hazard analysis / risk management and mitigation activities, the basic foundation of a viable CAPA system.
Wednesday, November 16, 2011
10: 00 AM PDT | 01: 00 PM EDT
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Root Cause Analysis - The Heart of a Successful CAPA Program - Webinar By GlobalCompliancePanel
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* ID / Document the Problem
* Investigation / Analysis Methodology - The 7 RCA "Tools"
* Find the Solution(s)
* Monitor for Effectiveness
* Lock In the Change - Close the Loop
* Take It to the Next Level
Who will benefit:
* Senior management in Drugs, Devices, Biologics, Dietary Supplements
* QA
* RA
* R&D
* Engineering
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