The 2-day seminar explains how to apply statistics to manage risk 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: ISO standards and FDA/MDD regulations regarding the use of statistics. Basic vocabulary and concepts. Statistical Process Control Statistical methods for Design Verification Statistical methods for Product/Process Qualification Metrology: the statistical analysis of measurement uncertainty, and how it is used to establish QC specifications How to craft statistically valid conclusion statements (e.g., for reports) Summary, from a risk management perspective Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900928SEMINAR?channel=mailer&camp=Seminar&AdGroup=allconferencealerts_MAY_2017_SEO

Date : 4th May 2017 to 5th May 2017

Place : United States, Houston, tx

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900928SEMINAR?channel=mailer&camp=Seminar&AdGroup=allconferencealerts_MAY_2017_SEO

Contact Person:Eevnt Manager

Description:

The 2-day seminar explains how to apply statistics to manage risk 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: ISO standards and FDA/MDD regulations regarding the use of statistics. Basic vocabulary and concepts. Statistical Process Control Statistical methods for Design Verification Statistical methods for Product/Process Qualification Metrology: the statistical analysis of measurement uncertainty, and how it is used to establish QC specifications How to craft "statistically valid conclusion statements" (e.g., for reports) Summary, from a risk management perspective Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900928SEMINAR?channel=mailer&camp=Seminar&AdGroup=allconferencealerts_MAY_2017_SEO

The 2-day seminar explains how to apply statistics to manage risk 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: ISO standards and FDA/MDD regulations regarding the use of statistics. Basic vocabulary and concepts. Statistical Process Control Statistical methods for Design Verification Statistical methods for Product/Process Qualification Metrology: the statistical analysis of measurement uncertainty, and how it is used to establish QC specifications How to craft statistically valid conclusion statements (e.g., for reports) Summary, from a risk management perspective Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900928SEMINAR?channel=mailer&camp=Seminar&AdGroup=allconferencealerts_MAY_2017_SEO will be held in Houston, tx,United States on date 2017-05-05

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Deadline for abstracts/proposals : 3rd May 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 :Houston, TX, United States

Check the event website for more details.