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DTSTAMP:20260415T125848Z
SUMMARY:Webinar On \"Corrective and Preventive Action utilizing the pr
 inciples of Lean Documents and Lean Configuration\"
DESCRIPTION:\nDescription :\nThe Theory of Lean Documents is the produ
 ct of applying lean principles to the creation, design, process, and m
 anagement of controlled documents typically found in regulated industr
 ies. Just as lean principles challenge traditional process concepts an
 d \"push\" systems, many traditional document practices are artifacts 
 of a flawed approach. Lean documents presents a fresh departure from t
 hese practices, while building upon proven principles. Lean configurat
 ion comes from the same principles, utilizing the unique power of soft
 ware solutions to take over functions that had previously burdened con
 trolled \"paper\" documents.  Why should you attend :\nMedical Device 
 managers, engineers, QA personnel, as well as lean program leaders.   
 Do you find yourself constantly struggling to create, manage, and main
 tain all of the information found in DHFs, DMRs, and DHRs - which is o
 ften redundant, repetitive, and chained together in a cumbersome way? 
 Do you find that your design and manufacturing resources are spending 
 way too much time on documentation and not enough on engineering and d
 esign? This webinar presents a fresh new approach based upon solid pri
 nciples and proven practices - as well as an alternative that avoids m
 any of the pitfalls of traditional ways of preparing these documents. 
 \n\n\n\n\nAreas Covered in the Session :\n\nBrief introduction to Lean
  Documents and Lean Configuration\nQuality System Regulation, 21 CFR P
 art 820, and ISO 13485 as it applies to Corrective and Preventive Acti
 on\nAlignment of the Six Sigma DMAIC approach to CAPA\nApplying lean p
 rinciples to instituting corrective and preventive actions\n\n\n\n\n\n
 Who Will Benefit:\nManagers, Supervisors, Directors, and Vice-Presiden
 ts in the areas of:\nR&D\nManufacturing Engineering\nDesign Assurance\
 nQuality Assurance\nOperations\nDocument Control\n\n\n\n\n\nAbout Spea
 ker:\nJosé Mora is a Principal Consultant and Project Manager special
 izing in Manufacturing Engineering, Quality Systems, and Lean Transfor
 mations. José is a recognized subject matter expert in process valida
 tion, lean manufacturing, lean controlled document systems, startup op
 erations, process development and quality systems, having lectured int
 ernationally and presented webinars on these subjects.\n\n\n\n\n\n\nFo
 r more information visit https://medtechiq.ning.com/events/webinar-on-
 corrective-and-preventive-action-utilizing-the
DTSTART;TZID=America/New_York:20180207T130000
DTEND;TZID=America/New_York:20180207T143000
CATEGORIES:online, "/", webinar
LOCATION:Online
WEBSITE:http://bit.ly/2BIok0o
URL:http://bit.ly/2BIok0o
CONTACT:1-844-216-5230
ORGANIZER;CN="Sam Miller":https://medtechiq.ning.com/profile/SamMiller
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562015929?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Sam Mill
 er":https://medtechiq.ning.com/profile/SamMiller
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