Effective Corrective And Preventive Actions (CAPA): 10 Steps to Success

This 120-minute webinar will explain all elements of CAPA process steps as required by ISO and regulatory agencies. In addition, it will be presented in a practical and proven manner, which can be immediately applied in your organization.

Why Should You Attend:

Organizations are pretty good when it comes to corrective actions, yet they are not nearly as good when it comes to the preventive actions. This webinar will provide you with enough ideas, suggestions and HOW TOs that you, your team and the organization overall get much better on the preventive actions and even better on the corrective actions. We will discuss all the elements of CAPA process steps as required by ISO and regulatory agencies. In addition, it is represented in a practical and proven manner which can be immediately applied in your organization.

Areas Covered in the Seminar:

• CAPA Process Steps include all elements.
• Quality Tools For Problem Identification and Definition.
• Verification and Validations of Actions Taken.
• CAPA Ownership and Assignment.
• Corrections versus Corrective Actions.
• Closure and Recognitions.
• Continuous Improvement.

Who Will Benefit:

• Product development engineers
• Quality Engineers
• Quality Managers
• Internal and External Quality Auditors
• Management Representatives
• FDA inspectors
• CAPA investigators
• Project managers
• Consultants
• AdvaMed companies

Event Details:

Date:              September 25, 2012

Time:              09:00 AM - 11:00 AM PDT

Cost:              $299 per attendee per computer terminal

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