Powerful Closed-loop CAPA - Meeting FDA Expectations

This 90-minute webinar will show how you can implement a closed-loop CAPA system that meets CGMP requirements and U.S. FDA expectations. You will learn simple, but powerful, tools and methods that you can use regularly and systematically to define and resolve root causes, not just symptoms.

Why Should You Attend:

The most important area audited by the FDA is CAPA - it assures the FDA that companies are in compliance without the agency constantly auditing it.

Closed-loop CAPA mandates a repeatable, systematic failure investigation and root cause analysis - define, locate and resolve the basic problem(s) or root cause(s). A full-capture investigation, verification/validation, monitoring, change control methodology, coupled with accurate root cause analysis is crucial to a closed-loop CAPA system, that meets / exceeds CGMP requirements and U.S. FDA expectations.

Who Will Benefit:

This webinar will provide valuable assistance to all regulated companies that need a repeatable methodology / defined systems, and simple but powerful tools for closed-loop CAPA, including proper failure investigation / root cause analysis and making the fix permanent. This applies to companies in the medical device, diagnostic, pharmaceutical, and biologics fields. The employees who will benefit include:

• Senior management
• Regulatory affairs
• Quality assurance
• Production
• R&D and engineering

Instructor Profile: 

John E. Lincoln is principal of J. E. Lincoln and Associates LLC, a consulting company, with over 33 years’ experience in U.S. FDA-regulated industries and 20 years as a full-time consultant. He has worked with companies from start-up to Fortune 100, in the U.S., Mexico, Canada, France, Germany, Sweden, China and Taiwan.

Note:

Use coupon code NB5SQH8N and get 10% off on registration.

For Registration:

http://www.complianceonline.com/capa-failure-investigation-and-root-cause-analysis-fda-expectations-webinar-training-702012-prdw?channel=sciencedz