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 them.
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, and 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.
This webinar will present simple but powerful tools, the systematic and regular use of which, can resolve the key underlying problem and close out CAPA documents in a timely manner. The information and tools presented in this webinar can contribute greatly to the reduction of product liability, cost reduction efforts, less chance of recalls, and an improved bottom line.
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:
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