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DTSTART:19700308T020000
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UID:2140535:Event:72119
DTSTAMP:20260520T180606Z
SUMMARY:Quality by Design using Design of Experiments (QbD) 2017
DESCRIPTION:\nCourse \"Quality by Design using Design of Experiments (
 QbD)\" has been pre-approved byÂ RAPSÂ as eligible for up toÂ 12Â cred
 its towards a participant's RAC recertification upon full completion\n
 Â \nOverview:\nThis seminar focuses on how to establish a systematic a
 pproach to pharmaceutical development that is defined by Quality-by-De
 sign (QbD) principles using design of experiments (DOE). In addition, 
 this course teaches the application of statistics for setting specific
 ations, assessing measurement systems (assays), developing a control p
 lan as part of a risk management strategy, and ensuring process contro
 l/capability. All concepts are taught within the product quality syste
 m framework defined by requirements in regulatory guidance documents.\
 nUsing a QbD approach for pharmaceutical development studies should in
 clude a systematic understanding of the process and using this underst
 anding to establish a control strategy as part of a comprehensive qual
 ity risk management program.\nThis systematic understanding should inc
 lude both identification of significant process parameters and determi
 nation of a functional relationship (mathematical model) linking these
  significant process parameters to the critical quality attributes (CQ
 As). The original guidance document on pharmaceutical development prov
 ides general guidance on how these are identified: gaining knowledge a
 bout which variation in factors explains variation in product quality 
 characteristics of drug product. It also provides a means to achieving
  this knowledge: through the use of formal experimental designs. The u
 se of DOE methodology provides a means to identify those factors that 
 impact product quality characteristics of drug product (or significant
  process parameters) and determine the functional relationship that li
 nks the process parameters to the CQAs.\n\nÂ \nLocation:Â Baltimore, M
 D Date: April 6th & 7th, 2017 and Time: 9:00 AM to 6:00 PM\nVenue: The
  DoubleTree Baltimore-BWI Airport\nAddress: The DoubleTree Baltimore-B
 WI AirportÂ Â  890 Elkridge Landing Road - Linthicum, MD 21090\nÂ \nPr
 ice:\nÂ \nRegister now and save $200. (Early Bird)\nÂ \nPrice: $1,295.
 00 (Seminar Fee for One Delegate)\nÂ \nUntil February 28, Early Bird P
 rice: $1,295.00 from March 01 to April 04, Regular Price: $1,495.00\nÂ
  \nRegister for 5 attendeesÂ Â  Price: $3,885.00 $6,475.00 You Save: $
 2,590.00 (40%)*\nÂ \nÂ \nQuick Contact:\nNetZealous DBA as GlobalCompl
 iancePanel\nPhone: 1-800-447-9407\nFax: 302-288-6884\nEmail: support@g
 lobalcompliancepanel.com Â Â Â Â Â Â Â Â Â Â Â Â Â Â \n\nÂ \nFollow us
  on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel?\
 nLike us our Facebook page: https://www.facebook.com/TrainingsAtGlobal
 CompliancePanel/\nFollow us on Twitter: https://twitter.com/GCPanel\nÂ
  \n\nÂ \n\nFor more information visit https://medtechiq.ning.com/event
 s/quality-by-design-using-design-of-experiments-qbd-2017
DTSTART;TZID=America/New_York:20170406T090000
DTEND;TZID=America/New_York:20170407T180000
CATEGORIES:quality, by, design, using, of, experiments, "(qbd)", 2017
LOCATION:Baltimore, MD
WEBSITE:http://www.globalcompliancepanel.com/control/globalseminars/~p
 roduct_id=900802SEMINAR?channel=mailer&camp=Seminar&AdGroup=medtechiq_
 April_2017_SEO
URL:http://www.globalcompliancepanel.com/control/globalseminars/~produ
 ct_id=900802SEMINAR?channel=mailer&camp=Seminar&AdGroup=medtechiq_Apri
 l_2017_SEO
CONTACT:800-447-9407
ORGANIZER:NetZealous DBA as GlobalCompliancePanel
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562032911?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="John Rob
 inson":https://medtechiq.ning.com/profile/JohnRobinson
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