The 2-day seminar explains how to apply statistics to manage risks and verify/validate processes in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry. The flow of topics over the 2 days is as follows:

Date : 13th July 2017 to 14th July 2017

Place : United States, Sfo, ca

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901084SEMINAR?allconferencealerts_july_2017_SEO

Contact Person:Eevnt Manager

Description:

The 2-day seminar explains how to apply statistics to manage risks and verify/validate processes in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry. The flow of topics over the 2 days is as follows:

The 2-day seminar explains how to apply statistics to manage risks and verify/validate processes in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry. The flow of topics over the 2 days is as follows: will be held in Sfo, ca,United States on date 2017-07-14

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Deadline for abstracts/proposals : 11th July 2017

Keynote Speakers : John N. Zorich, has spent 35 years in the medical device manufacturing industry; the first 20 years were as a "regular" employee in the areas of R&D, Manufacturing, QA/QC, and Regulatory; the last 15 years were as consultant in the areas of QA/QC and Statistics. His consulting clients in the area of statistics have included numerous start-ups as well as large corporations such as Boston Scientific, Novellus, and Siemens Medical. His experience as an instructor in statistics include

Conference Highlights :QA/QC Supervisor Process Engineer Manufacturing Engineer QC/QC Technician Manufacturing Technician R&D Engineer

Venue :San Francisco Airport, San Francisco, CA, United States

Check the event website for more details.