Incorporating Six Sigma DMAIC into CAPA -Webinar By GlobalCompliancePanel

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Incorporating Six Sigma DMAIC into CAPA
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Course "Incorporating Six Sigma DMAIC into CAPA" has been

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pre-approved by RAPS as eligible for up to 1.00 credits towards
a participant's RAC recertification upon full completion.

Instructor Profile:
Thursday, September 13, 2012
10:00 AM PDT | 01:00 PM EDT
Duration: 60 Minutes
Instructor: Jose Mora
Jose Mora
Principal Consultant, Atzari
Location: Online
Price : $245.00 (for one participant)
Consulting, LLC

JoseMora is a Principal Consultant
specializing in Manufacturing
Design History Files (DHF), Device Master Records (DMR), and Device
Engineering and Quality Systems.
History Records (DHR) are key building blocks used in the design,
For over 29 years he has worked in
development, manufacturing, and cGMP compliance for the Medical
the medical device industry
Device Industry. Too often, these are cluttered, confusing, and cause
specializing in manufacturing,
process development, tooling, and
many errors due to the way they are created, organized, and
quality systems. Prior to working full
time as a consulting partner for

This webinar applies the Theory of Lean Documents and also
Director of Manufacturing
formulates a corresponding Theory of Lean Configuration to these
Engineering at Boston Scientific and
key elements of medical device documents.
as Quality Systems Manager at

Stryker Orthopedics, where he
introduced process performance,
Why Should You Attend:
problem solving, and quality system
Do you find yourself constantly solving the same problems only to
methodologies. During that time he
have them re-appear? Do you feel that something is amiss when

prepared a white paper on the
application of lean manufacturing
your metrics tell you one thing, but the reality is that you are living
methods to the creation and
with problems? There is a different approach to Corrective and
management of controlled
PreventiveAction.Thiswebinarshowshowto ensure that problems
documents and a template for
are replaced with reliable processes and systems.
strategic deployment.Joseledthe

launch of manufacturing at a start-up
urology products company as
Areas Covered in the Session:
Director of Manufacturing for
UroSurge, Inc. at the University of
Brief introduction to Lean Documents and Lean Configuration
Iowa's business incubator park in
Coralville, IA, creating a world-class
Quality System Regulation, 21 CFR Part 820, as it applies to
medical device manufacturing
operation, with JIT, kanban systems,
The Six Sigma DMAIC process
visual workplace and lean
Types of Corrective and Preventive Actions
manufacturing practices.Jose
Integration of DMAIC into the CAPA process
worked for 10 years at Cordis
Corporation, now a Johnson &
Johnson company, where he led the
Click here to register for this webinar
successful tooling, process ...more
Who Will Benefit:
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Manufacturing Engineering
Quality Assurance
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benefit from this program.

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

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