Docstoc

Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration

Document Sample
Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration Powered By Docstoc
					                                                                                                                                        


    Live Webinar            on

        Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean
        Documents and Lean Configuration

    Date & Time:                                                                                                                         

        Tuesday, July 12, 2011             10:00 AM PDT | 01:00 PM EDT
                                                                                                    Register Now                            
        Duration: 60 Minutes               Instructor: Jose Mora

        Location: Online                   Price : $245.00   (for one participant)

                                                                                              Instructor Profile:

        Overview:
                                                                                                              Jose Mora
    Design History Files (DHF), Device Master Records (DMR), and Device                               Principal Consultant, Atzari
    History Records (DHR) are key building blocks used in the design,                                       Consulting, LLC
    development, manufacturing, and cGMP compliance for the Medical
    Device Industry.                                                                          José Mora is a Principal Consultant
                                                                                              specializing in Manufacturing
    Too often, these are cluttered, confusing, and cause many errors due                      Engineering and Quality Systems.
    to the way they are created, organized, and managed. This webinar                         For over 29 years he has worked in
                                                                                              the medical device industry
    applies the Theory of Lean Documents and also formulates a
                                                                                              specializing in manufacturing,
    corresponding Theory of Lean Configuration to these key elements of
                                                                                              process development, tooling, and
    medical device documents.                                                                 quality systems. Prior to working full
                                                                                              time as a consulting partner for
                                                                                              Atzari Consulting, José served as
        Areas Covered in the Session:
                                                                                              Director of Manufacturing
                                                                                              Engineering at Boston Scientific and
          l   Brief introduction to Lean Documents and Lean Configuration                     as Quality Systems Manager at
          l   Quality System Regulation, 21 CFR Part 820, as it applies to                    Stryker Orthopedics, where he
              DHF, DMR, and DHR                                                               introduced process performance,
                                                                                              problem solving, and quality system
          l   Design History Files (DHF) content, development, and
                                                                                              methodologies. During that time he
              management
                                                                                              prepared a white paper on the
          l   Device Master Records (DMR) content, development, and                           application of lean manufacturing
              management                                                                      methods to the creation and
          l   Device History Record (DHR) content, development, and                           management of controlled
              management                                                                      documents and a template for
          l   Applying lean principles to creating, developing, and managing                  strategic deployment. José led the 
              a DHF                                                                           launch of manufacturing at a start-up
                                                                                              urology products company as
          l   Applying lean principles to creating, developing, and managing
                                                                                              Director of Manufacturing for
              a DMR
                                                                                              UroSurge, Inc. at the University of
          l   Applying lean principles to creating, developing, and managing                  Iowa’s business incubator park in
              DHRs                                                                            Coralville, IA, creating a world-class
                                                                                              medical device manufacturing
    Click here to register for this webinar                                                   operation, with JIT, kanban systems,
                                                                                              visual workplace and lean
                                                                                              manufacturing practices. ...more
        Who Will Benefit:

          l   Managers, Supervisors, Directors, and Vice-Presidents in the                   Suggest a Topic       More Webinars
              areas of:
          l   R&D                                                                              Your Necessity is our Priority
          l   Manufacturing Engineering
          l   Quality Assurance
          l   Operations
          l   Document Control
                                                                                                                
     

It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely
benefit from this program.

For more information, please contact the event coordinator. We look forward to seeing you at the webinar.

Best regards,
Event-coordinator
GlobalCompliancePanel



About GlobalCompliancePanel
GlobalCompliancePanel is an online knowledge fulfillment community portal & it has put together a new model for online
compliance training by creating a single window of learning opportunities for compliance professionals & providing a
forum for expert speakers/panelists to render their services through simplified online training delivery mechanisms. Our
commitment is give compliance regulatory training, showcasing of best industry practices & quality enrichment training
sessions in a most cost effective manner. Compliance professionals can benefit from a wide range of training sessions,
giving a diverse choice of events & all sessions being either Live or recorded stream or in the form of audio CDs.
GlobalCompliancePanel portal ensures a secure & cost effective online environment and also support your E-learning
and development on/through our website. Keep track of all webinars arranged for your industry through notifications &
event calendars being mailed to your inbox. GlobalCompliancePanel opens new doors of learning opportunities for
professionals.


GlobalCompliancePanel
www.globalcompliancepanel.com
1000 N West Street Suite,
1200 Wilmington DE 19801

Phone: 800-447-9407 or
Fax your PO to: 302-288-6884


If you do not wish to receive this training alerts from GlobalCompliancePanel Click Unsubscribe

				
DOCUMENT INFO
Shared By:
Stats:
views:47
posted:6/9/2011
language:English
pages:2
Description: Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are key building blocks used in the design, development, manufacturing, and cGMP compliance for the Medical Device Industry. Too often, these are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed. This webinar applies the Theory of Lean Documents and also formulates a corresponding Theory of Lean Configuration to these key elements of medical device documents