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DTSTART:19700308T020000
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UID:2140535:Event:65821
DTSTAMP:20260521T003903Z
SUMMARY:Applied Statistics for Scientists and Engineers at Zurich, Swi
 tzerland
DESCRIPTION:Throughout 21 CFR and guidance documents for the pharmaceu
 tical, biopharmaceutical, and medical device industries, the applicati
 on of statistical methods are specified for: setting validation criter
 ia and specifications, performing measurement systems analysis (MSA), 
 conducting stability analysis, using design of experiment (DOE) for pr
 ocess development and validation, developing process control charts, a
 nd determining process capability indices.\nDifferent statistical meth
 ods are required for each of these particular applications. Data and t
 olerance intervals are common tools used for setting acceptance criter
 ia and specifications. Simple linear regression and analysis-of-covari
 ance (ANCOVA) are used for setting expiries and conducting stability a
 nalysis studies. Two-sample hypothesis tests, analysis-of-variance (AN
 OVA), regression, and ANCOVA are methods used for analyzing designed e
 xperiment for process development and validation studies. Descriptive 
 statistics (distribution, summary statistics), run charts, and probabi
 lity (distributions) are used for developing process control charts an
 d developing process capability indices.\nAreas Covered in the Session
 :\nObjectives:\n\ndescribe and analyze the distribution of data\ndevel
 op summary statistics\ngenerate and analyze statistical intervals and 
 hypothesis tests to make data-driven decisions\ndescribe the relations
 hip between and among two or more factors or responses\nunderstand iss
 ues related to sampling and calculate appropriate sample sizes\nuse st
 atistical intervals to setting specifications/develop acceptance crite
 ria\nuse Measurement Systems Analysis (MSA) to estimate variance assoc
 iated with: repeatability, intermediate precision, and reproducibility
 \nensure your process is in (statistical) control and capable\n\nWho W
 ill Benefit:\nThis seminar is designed for pharmaceutical, biopharmace
 utical, and medical device professionals who are involved with product
  and/or process design:\n\nProcess Scientist/Engineer\nDesign Engineer
 \nProduct Development Engineer\nRegulatory/Compliance Professional\nDe
 sign Controls Engineer\nSix Sigma Green Belt\nSix Sigma Black Belt\nCo
 ntinuous Improvement Manager\n\nSpeaker:\nDr. Heath Rushing, is the c
 ofounder of Adsurgo and author of the book Design and Analysis of E
 xperiments by Douglas Montgomery: A Supplement for using JMP. Previou
 sly, he was the JMP and Six Sigma training manager at SAS. \nPrice: $
 2,095.00 (Seminar for One Delegate)\nRegister now and save $200. (Earl
 y Bird)\nUntil June 10, Early Bird Price: $2,095.00\nFrom June 11 to J
 uly 14, Regular Price: $2,295.00\nContact Information:\nNetZealous LLC
 ,\nDBA GlobalCompliancePanel\n161 Mission Falls Lane,\nSuite 216, Frem
 ont, CA 94539, USA         \nUSA Phone: 800-447-9407\nFax: 30
 2-288-6884\nsupport@globalcompliancepanel.com          \nhtt
 p://www.globalcompliancepanel.com\nEvent Registration Link - http://bi
 t.ly/1OwI6ew\n\nFor more information visit https://medtechiq.ning.com/
 events/applied-statistics-for-scientists-and-engineers-at-zurich
DTSTART;TZID=America/New_York:20150716T090000
DTEND;TZID=America/New_York:20150717T180000
CATEGORIES:clinical, food, fda, medical, device, defence, and, navy, a
 erospace, mining
LOCATION:Zurich, Switzerland
WEBSITE:https://www.globalcompliancepanel.com
URL:https://www.globalcompliancepanel.com
CONTACT:18004479407
ORGANIZER:GlobalCompliancePanel
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562011438?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="John Rob
 inson":https://medtechiq.ning.com/profile/JohnRobinson
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