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DTSTART:19700308T020000
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UID:2140535:Event:56411
DTSTAMP:20260516T030432Z
SUMMARY:Powerful Closed-loop CAPA - Meeting FDA Expectations
DESCRIPTION:This 90-minute webinar will show how you can implement a c
 losed-loop CAPA system that meets CGMP requirements and U.S. FDA expec
 tations. You will learn simple, but powerful, tools and methods that y
 ou can use regularly and systematically to define and resolve root cau
 ses, not just symptoms.\nWhy Should You Attend:\nThe most important ar
 ea audited by the FDA is CAPA - it assures the FDA that company is in 
 compliance without the Agency constantly auditing it.\nClosed-loop CAP
 A mandates a repeatable, systematic Failure Investigation and Root Cau
 se Analysis - define, locate and resolve the basic problem(s) or root 
 cause(s). A full-capture investigation, verification/validation, monit
 oring, change control methodology, coupled with accurate root cause an
 alysis is crucial to a \"closed-loop\" CAPA system, that meets / excee
 ds CGMP requirements and U.S. FDA expectations.\n\n\nFor more informat
 ion visit https://medtechiq.ning.com/events/powerful-closed-loop-capa-
 meeting-fda-expectations
DTSTART;TZID=America/New_York:20120807T100000
DTEND;TZID=America/New_York:20120807T113000
CATEGORIES:medical, training
LOCATION:Online Event
WEBSITE:http://www.complianceonline.com/ecommerce/control/trainingFocu
 s/~product_id=702012?channel=MedtechIQ
URL:http://www.complianceonline.com/ecommerce/control/trainingFocus/~p
 roduct_id=702012?channel=MedtechIQ
CONTACT:+1-650-620-3915
ORGANIZER;CN=Referral:https://medtechiq.ning.com/profile/Referral
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562006613?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Referral:
 https://medtechiq.ning.com/profile/Referral
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