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June 1, 2018 - December 31, 2019

Root Cause Analysis and CAPA Controls for a Compliant Quality System

United States

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Event Details

Begins: June 1, 2018

End: December 31, 2019

Event Location: United States

Website: https://www.compli..5698-prdw

Event Organizer

Event Organizer: ComplianceOnline

Contact Person: Sreeraj Mathilassery

Phone Number: +1-888-717-2436

Website: https://www.complianceonline.com/

Overview

In this CAPA webinar, learn various regulations governing Corrective and Preventive Actions (CAPA) and how organization should collect information, analyze information, identify, investigate product and quality problems, and take appropriate and effective corrective and/or preventive action to prevent their recurrence.

Why Should You Attend:

As simple as it sounds, the Root Cause Analysis and CAPA has always posed challenges to the organization and has been the #1 reason for 483 observations and Warning Letters for the last 15 years. Strong CAPA controls make an organization compliant and less vulnerable to customer complaints, nonconformance, deviations, etc. The CAPA controls rely on three important concepts namely, remedial correction; understanding the root cause and come up with corrective actions; and to have preventive actions to avert recurrence. If the root cause analysis is not done correctly, all the subsequent steps towards correction and prevention would be rendered ineffective and cause the issue to reoccur.

You will learn insights into root cause analysis and develop a logical approach to problem solving by accurately identifying causes of problems and have permanent solutions in place. This would help drive compliance and towards an organizational success.

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