CAPA within a Device Quality System - 2017

You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you.

Why should you Attend:

Corrective and Preventive Action (CAPA) is the cornerstone of a strong Quality Management System. And yet, many medical device manufacturers struggle to establish and maintain and effective CAPA process.

Areas Covered in the Session:

• FDA and NB expectations for CAPA
• Lessons Learned from 483s and warning letters
• Common problems CAPA
• How to structure your CAPA process
• How to use IT tools to monitor and maintain your CAPAs
• Metrics to ensure your CAPAs are timely and effective
• A toolkit for CAPA
• Best Practices

Who Will Benefit:

• Quality Systems Specialists
• Document Control Specialists
• Quality and Compliance Specialists
• Internal Auditors and Managers
• Training Specialists
• CAPA Specialists