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DTSTAMP:20260521T024918Z
SUMMARY:Webinar On \"Supplier Quality Management Utilizing Principles 
 of Lean Documents and Lean Configuration\"
DESCRIPTION:\nDescription :\nAll life science businesses are required 
 to maintain their Quality Management System (QMS) processes in a state
  of control, via controlled documents and objective evidence in the fo
 rm of records.  Utilizing suppliers as an extension of an organization
 ´s design and manufacturing capabilities presents unique challenges.\
 nBackground :\nMany companies have outsourced both their design and ma
 nufacturing to specialized suppliers.  As new medical device technolo
 gies push the boundaries of miniaturization, 3D printing and solid mod
 eling, imaging, drug-device combinations, and new applications, the de
 mand for specialized suppliers has left gaps in the common understandi
 ng of medical device requirements.  Also, changes to ISO 13485:2016 h
 ave required a risk-based approach to all QMS processes – including 
 those associated with supplier management and processes associated wit
 h them.\nWhy should you attend - Fear, uncertainty and doubt (FUD) lin
 er for the marketing purpose :\nChanges in technologies and supply-cha
 in arrangements have coincided with the expansion of regulations and s
 tandards to the entire supply chain.  Unfortunately, many suppliers h
 ave not kept up or find themselves in a strange new world.\nRather tha
 n wait to be surprised by unexpected situations, or to implement requi
 rements haphazardly, it is better to understand what the hands-on chal
 lenges of dynamic cross-functional and cross-organizational teams as t
 hey push the boundaries of technology and new applications.\nThis webi
 nar is an overview of the coming changes and their implications, using
  a new approach yet is based upon solid principles and proven practice
 s.\n\n\n\n\n\nAreas Covered in the Session :\nReview of Lean Documents
  and Lean Configuration concepts;\nOverview of Supplier Quality Manage
 ment:\n\nBasics of supplier quality management\nIssues around design c
 ontrols and design freeze\nIssues around manufacturing and quality met
 rics\nAlignment of supplier to designer/manufacturer\nRisk management 
 including risk mitigation\nRisks around supplier quality during design
  changes\nRisk Management File and Design History File\n\n\n\n\n\nWho 
 Will Benefit:\nManagers, Supervisors, Directors, and Vice-Presidents i
 n the areas of: • R&D • Manufacturing Engineering • Design Assur
 ance • Quality Assurance • Operations • Document Control\n\n\n\n
 \nAbout Speaker:\nJosé Mora is a Principal Consultant and Project Man
 ager specializing in Manufacturing Engineering, Quality Systems, and L
 ean Transformations. José is a recognized subject matter expert in pr
 ocess validation, lean manufacturing, lean controlled document systems
 , startup operations, process development and quality systems, having 
 lectured internationally and presented webinars on these subjects.\n\n
 \n\n\n\n\nFor more information visit https://medtechiq.ning.com/events
 /webinar-on-supplier-quality-management-utilizing-principles-of
DTSTART;TZID=America/New_York:20180109T130000
DTEND;TZID=America/New_York:20180109T143000
CATEGORIES:online, "/", webinar
LOCATION:Online
WEBSITE:http://bit.ly/2E5Irrw
URL:http://bit.ly/2E5Irrw
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/2562016311?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Sam Mill
 er":https://medtechiq.ning.com/profile/SamMiller
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