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UID:2140535:Event:71734
DTSTAMP:20260406T203347Z
SUMMARY:Design of Experiments (DOE) for Process Development and Valida
 tion 2017
DESCRIPTION:Course \"Design of Experiments (DOE) for Process Developme
 nt and Validation\" has been pre-approved by RAPS as eligible for up t
 o 12 credits towards a participant's RAC recertification upon full com
 pletion.\nOverview: Prior to developing a process control plan as part
  of an overall risk management strategy, process development studies m
 ust be completed. The objective of these process development studies i
 s to gain knowledge and understanding about how variation in process p
 arameters explains variation in the product quality characteristics of
  the product.\nThe use of DOE methodology provides a means to identify
  process parameters which impact product quality (critical process par
 ameters) and determine the functional relationship that links the proc
 ess parameters to those critical quality attributes. Screening designs
 , such as 2k factorial and D-optimal designs, are used to determine cr
 itical process parameters. Response surface designs, such as Central C
 omposite Designs (CCDs) and I-optimal designs, are used to model the f
 unctional relationship between those critical process parameters and t
 he critical quality attributes.\nThis course will begin by presenting 
 a primer on statistical analysis, focusing on the methods required for
  analysis of designed experiments. It will then present the steps to D
 OE, while demonstrating valuable risk management tools (Ishikawa and F
 MEA) which can be use pre and post DOE studies. Next, participants wil
 l learn to generate and analyze multiple screening and response surfac
 e designs; the participants will leave with an understanding of why an
 d how each are used. Then, the participants will learn how results of 
 the studies can be presented. Lastly, using the results of the studies
 , the risk management tools will then be updated.\n \n\nLocation: Lo
 s Angeles, CA Date: March 30th & 31st, 2017 and Time: 9:00 AM to 6:00 
 PM\n \nVenue: Four Points by Sheraton Los Angeles International Airpo
 rt\nAddress: 9750 Airport Boulevard, Los Angeles, CA, 90045, United St
 ates\n \nPrice:\n \nPrice: $1,295.00 (Seminar Fee for One Delegate)\
 nUntil February 20, Early Bird Price: $1,295.00 from February 21 to Ma
 rch 28, Regular Price: $1,495.00\nRegister for 5 attendees Price: $3,8
 85.00 $6,475.00 You Save: $2,590.00 (40%)*\n \nQuick Contact:\nNetZea
 lous DBA as GlobalCompliancePanel\n \nPhone: 1-800-447-9407\nFax: 302
 -288-6884\nEmail: support@globalcompliancepanel.com     \n\n\n\nFo
 r more information visit https://medtechiq.ning.com/events/design-of-e
 xperiments-doe-for-process-development-and-validatio-1
DTSTART;TZID=America/New_York:20170330T090000
DTEND;TZID=America/New_York:20170331T180000
CATEGORIES:compliance, training, and, latest, information
LOCATION:Los Angeles, CA
WEBSITE:http://www.globalcompliancepanel.com/control/globalseminars/~p
 roduct_id=900794SEMINAR?channel=mailer&camp=Seminar&AdGroup=medtechiq_
 March_2017_SEO.
URL:http://www.globalcompliancepanel.com/control/globalseminars/~produ
 ct_id=900794SEMINAR?channel=mailer&camp=Seminar&AdGroup=medtechiq_Marc
 h_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/2562014850?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="John Rob
 inson":https://medtechiq.ning.com/profile/JohnRobinson
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