Date :
Place : United States, Doubletree by hilton houston intercontinental airport
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: ISO standards and FDA/MDD regulations regarding the use of statistics. Basic vocabulary and concepts, including distributions such as binomial, hypergeometric, and Normal, and transformations into Normality. Statistical Process Control Statistical methods for Design Verification Statistical methods for Product/Process QualificationDeadline for abstracts/proposals : 5th December 2017
Organized By :NetZealous DBA as GlobalCompliancePanel
Keynote Speakers : John N. Zorich Statistical Consultant & Trainer, Ohlone College & SV Polytechnic 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 Sc
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.