FDA COMPLIANCE 2011 - Closed-Loop CAPA - Meeting FDA Requirements - Webinar by ComplianceOnline

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Category Closed-loop CAPA;FDA Requirements; Closed-loop CAPA System; CAPA tools; root-cause analysis

Deadline: October 18, 2011 | Date: October 18, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2011-10-04 13:57:34 (GMT+9)

Call For Papers - CFP

This CAPA training will provide 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.

Why Should You Attend:

Repeatable, systematic Failure Investigation and Root Cause Analysis is an often discussed, but little understood discipline among those who could benefit most from its use. The most important area audited by the FDA is CAPA. One of the most cited 483 observation is failure to resolve the key underlying problem and close out CAPA documents in a timely manner -- basically an inability to define, locate and resolve the basic problem(s) or root cause(s).

This webinar will show how regular, defined and systematic use of a few simple but powerful tools can contribute greatly to reduction of product liability, cost reduction efforts, less chance of recalls, and an improved bottom line.