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DTSTAMP:20260513T113426Z
SUMMARY:Webinar on Design Inputs - Design Outputs Traceability Matrix
DESCRIPTION:Overview: \nDesign Inputs, Design Outputs, and Traceabili
 ty matrices present a challenge to almost all industries that apply de
 sign controls.\nTypically, these cause the creation and maintenance of
  duplicate information across various documents - a major source of er
 rors. This webinar applies the Theory of Lean Documents and the corres
 ponding Theory of Lean Configuration to avoiding these errors, while p
 resenting a fresh new approach to these key and related documents.Why 
 you should attend:\nDo you find yourself constantly struggling to crea
 te, manage, and maintain all of the information found in Design Inputs
 , Design Outputs, and traceability matrices - which is often redundant
 , repetitive, and chained together in a cumbersome way? Do you find th
 at your design and manufacturing resources are spending way too much t
 ime on documentation and not enough on engineering and design? This we
 binar presents a fresh new approach based upon solid principles and pr
 oven practices - as well as an alternative that avoids many of the pit
 falls of traditional ways of preparing these documents.\nAreas Covered
  In the Session:\n\nBrief introduction to Lean Documents and Lean Conf
 iguration\nQuality System Regulation, 21 CFR Part 820, and ISO 13485 a
 s these apply to design control documents.\nDesign Inputs - User Requi
 rements Specification; Technical Design Requirements\nDesign Outputs -
  Specifications, Drawings, Documents\nTraceability Matrix\nApplying le
 an document and lean configuration principles to the above\nBringing i
 t all together\n\nWho will benefit:\n\nManagers, Supervisors, Director
 s, and Vice-Presidents in the areas of:\nR&D\nManufacturing Engineerin
 g\nQuality Assurance\nOperations\nDocument Control\n\nSpeaker Profile:
 \n\nJose Mora is a Principal Consultant specializing in Manufacturin
 g Engineering and Quality Systems. For over 30 years he has worked in 
 the medical device industry specializing in manufacturing, process dev
 elopment, tooling, and quality systems. Prior to working full time as 
 a consulting partner for Atzari Consulting, José served as Director o
 f Manufacturing Engineering at Boston Scientific and as Quality System
 s Manager at Stryker Orthopedics, where he introduced process performa
 nce, problem solving, and quality system methodologies.\n\nContact Det
 ail:\nCompliance4All DBA NetZealous,Phone: +1-800-447-9407Email: suppo
 rt@compliance4All.comhttp://www.compliance4all.com/Event Link : http:
 //bit.ly/Design_Outputs_Traceability\nLinkedIn Follow usTwitter Follow
  usFacebook Like us\n\n\n\nFor more information visit https://medtechi
 q.ning.com/events/webinar-on-design-inputs-design-outputs-traceability
 -matrix
DTSTART;TZID=America/New_York:20160503T100000
DTEND;TZID=America/New_York:20160503T110000
CATEGORIES:webinar
LOCATION:Online Event
WEBSITE:http://bit.ly/Design_Outputs_Traceability
URL:http://bit.ly/Design_Outputs_Traceability
CONTACT:18004479407
ORGANIZER;CN="Adam Fleming":https://medtechiq.ning.com/profile/Complia
 nce4all
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562012364?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle
 ming":https://medtechiq.ning.com/profile/Compliance4all
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