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DTSTART:19700308T020000
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UID:2140535:Event:240186
DTSTAMP:20260415T053208Z
SUMMARY:Death By CAPA - Does your CAPA Program Need a CAPA?
DESCRIPTION:This webinar will help you establish an efficient and effe
 ctive CAPA (Corrective and Preventive Action) process leading to impro
 ved quality and compliance for your company.\nYou'll learn how to stre
 amline and monitor your process to ensure compliance and improved perf
 ormance. If your CAPA process needs a CAPA, this webinar is for you. W
 e will discuss requirements, the myths, and the challenges of managing
  CAPAs so you can avoid common problems and pitfalls.We'll discuss bes
 t practices so you can start off on the right foot and always be prepa
 red for an inspection.Why you should Attend:CAPA is the corner stone o
 f an effective Quality Management System. Yet, it frequently perceived
  as a burdensome and bureaucratic exercise. Many companies struggle to
  establish and maintain a CAPA program that is efficient and effective
 . An ineffective CAPA System leads to disastrous consequences such as 
 medical device reports, recalls, 483s, and warning letters. And an ine
 fficient CAPA program results in wasted time, money, and missed opport
 unities. In this webinar, we'll discuss the fundamentals of a CAPA pro
 gram and how you can make your CAPA program more efficient and more ef
 fective.Areas Covered in the Session:\n\nFDA and NB expectations for C
 APA\nLessons Learned from 483s and warning letters\nCommon problems an
 d simple solutions\nHow to structure your CAPA process\nHow to use IT 
 tools to monitor and maintain your CAPAs\nMetrics to ensure your CAPAs
  are timely and effective\nA toolkit for CAPA\n\nLearning Objectives:\
 n\nOverview of the Regulations\nFDA Expectations\nLessons Learned and 
 Common Mistakes\nBest Practices\nPreparing for an FDA Inspection\n\nWh
 o Will Benefit:\n\nQuality Systems Specialists\nDocument Control Speci
 alists\nQuality and Compliance Specialists\nInternal Auditors and Mana
 gers\nTraining Specialists\nCAPA Specialists\nSupplier Quality Enginee
 rs and Auditors\nQuality/Compliance Managers or Directors for Medical 
 Device companies\nGeneral Managers wanting to learn how to understand 
 Quality System Requirements\n\n\n\n\nSpeaker ProfileSusanne Manz ,MBA
 , MBB, RAC, CQA is an accomplished leader in the medical device indust
 ry with emphasis on quality, compliance, and six sigma. She has an ext
 ensive background in quality and compliance for medical devices from n
 ew product development, to operations, to post-market activities. Whil
 e at GE, J&J, and Medtronic, Susanne worked in various world-wide role
 s including Executive Business Consultant, WW Director of Quality Engi
 neering and, Design Quality, and Director of Corporate Compliance. Sus
 anne has a BS in Biomedical Engineering and an MBA from the University
  of NM.\n\nEvent link:\nhttps://www.compliance4all.com/webinar/--50286
 2LIVE?channel=%20medtechiq.ning_2020_SEO\nContact Info\nNetzealous LLC
 ,DBA -Compliance4all\nEmail: support@compliance4All.com\nPhone: +1-800
 -447-9407\nWebsite: https://www.compliance4all.com/\n\n\n\nFor more in
 formation visit https://medtechiq.ning.com/events/death-by-capa-does-y
 our-capa-program-need-a-capa
DTSTART;TZID=America/New_York:20200225T100000
DTEND;TZID=America/New_York:20200225T130000
CATEGORIES:online, event
LOCATION:Online
WEBSITE:https://www.compliance4all.com/webinar/death-by-capa---does-yo
 ur-capa-program-need-a-capa--502862LIVE
URL:https://www.compliance4all.com/webinar/death-by-capa---does-your-c
 apa-program-need-a-capa--502862LIVE
CONTACT:+1-800-447-9407
ORGANIZER:Compliance4all
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/2647295700?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle
 ming":https://medtechiq.ning.com/profile/Compliance4all
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