This seminar focuses on how to establish a systematic approach to pharmaceutical development that is defined by Quality-by-Design (QbD) principles using Design of Experiments (DOE). In addition, this course teaches the application of statistics for setting specifications, assessing measurement systems (assays), developing a control plan as part of a risk management strategy, and ensuring process control/capability. All concepts are taught within the product Quality System framework defined by requirements in regulatory guidance documents. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901008SEMINAR?allconferencealerts_SEO

Date : 12th June 2017 to 13th June 2017

Place : Singapore, Singapore

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901008SEMINAR?allconferencealerts_SEO

Contact Person:Eevnt Manager

Description:

This seminar focuses on how to establish a systematic approach to pharmaceutical development that is defined by Quality-by-Design (QbD) principles using Design of Experiments (DOE). In addition, this course teaches the application of statistics for setting specifications, assessing measurement systems (assays), developing a control plan as part of a risk management strategy, and ensuring process control/capability. All concepts are taught within the product Quality System framework defined by requirements in regulatory guidance documents. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901008SEMINAR?allconferencealerts_SEO

This seminar focuses on how to establish a systematic approach to pharmaceutical development that is defined by Quality-by-Design (QbD) principles using Design of Experiments (DOE). In addition, this course teaches the application of statistics for setting specifications, assessing measurement systems (assays), developing a control plan as part of a risk management strategy, and ensuring process control/capability. All concepts are taught within the product Quality System framework defined by requirements in regulatory guidance documents. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901008SEMINAR?allconferencealerts_SEO will be held in Singapore,Singapore on date 2017-06-13

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Deadline for abstracts/proposals : 11th June 2017

Keynote Speakers : eath Rushing is the cofounder of Adsurgo LLC and co-author of the book Design and Analysis of Experiments by Douglas Montgomery: A Supplement for using JMP. Previously, he was the JMP and Six Sigma training manager at SAS. He led a team of nine technical professionals designing and delivering applied statistics and quality continuing education courses. He created tailored courses, applications, and long-term training plans in quality and statistics

Conference Highlights :Process Scientist/Engineer Design Engineer Product Development Engineer Regulatory/Compliance Professional Design Controls Engineer Six Sigma Green Belt

Venue :Singapore

Check the event website for more details.