2014 - Corrective and Preventive Action (CAPA)

Instructor: John Chapman
Description:
Corrective and Preventive Action (CAPA) is a requirement under international standards such as ISO 13485:2003 and FDA under 21CFR 820.
This presentation will define and explain the regulatory requirements and principles of Corrective Action and how they can benefit the organizationas well as the consequences of poor adherence to these principles.
Objectives of the Presentation:
Potential sources for CAPA
Root cause analysis
Effectiveness
Consequences of poor Corrective & Preventive Action
Why CAPA makes good business sense
Who can Benefit:
Companies wishing to understand the risks and complications involved with the application of sound verification and validation principles will gain a better understanding of the differences and benefits. Employees who will benefit include:
Quality & Regulatory Professionals
Manufacturing & Design Engineers
Marketing Product Managers
Corporate & Operations Executives
Register Now:
http://www.onlinecompliancepanel.com/ecommerce/web...
Online Compliance Panel LLC
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Fremont, CA, USA
94536
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