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Design of Experiments (DOE) for Process Development and Validation 2017

Start Date:
Thursday, 30 March, 2017
End Date:
Friday, 31 March, 2017 6:00pm
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Course "Design of Experiments (DOE) for Process Development and Validation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.Overview: Prior to developing a process control plan as part of an overall risk management strategy, process development studies must be completed. The objective of these process development studies is to gain knowledge and understanding about how variation in process parameters explains variation in the product quality characteristics of the product.The use of DOE methodology provides a means to identify process parameters which impact product quality (critical process parameters) and determine the functional relationship that links the process parameters to those critical quality attributes.

Screening designs, such as 2k factorial and D-optimal designs, are used to determine critical process parameters. Response surface designs, such as Central Composite Designs (CCDs) and I-optimal designs, are used to model the functional relationship between those critical process parameters and the critical quality attributes.This 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 DOE, while demonstrating valuable risk management tools (Ishikawa and FMEA) which can be use pre and post DOE studies. Next, participants will learn to generate and analyze multiple screening and response surface designs; the participants will leave with an understanding of why and 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.

Why should you attend?The Global Harmonization Task Force (GHTF) Process Validation Guidance for Medical Device Manufacturers provides guidance on where design of experiments should be applied during process validation; it suggests the use of both screening and response surface designs during Operational Qualification. In addition, DOE should be used during multiple phases of design controls: design and development planning, design verification, design validation, design transfer, and design changes.In Guidance for Industry Q8 Pharamaceutical Development (as well as the annex to Q8), suggests applying experimental design to demonstrate " enhanced knowledge of product performance over a range of...process parameters." Using this "...enhanced, quality by design approach..." leads to greater system understanding.

That greater system understanding has two elements: identifying critical process parameters and developing a functional relationship that link those critical process parameters to your critical quality attributes (CQAs). This suggests the use of both screening and response surface designs during pharmaceutical development studies.The need for DOE in product and process development is not only suggested, but imperative for both medical device and drug manufactures.

Areas Covered in the Session:Learn how to effectively use JMP to:identify critical quality attributes (CQAs) that will be used as responses in your designsutilize risk management tools to identify and prioritize potential critical process parametersidentify critical process parameters and develop a functional relationship between those process parameters and your critical-to-quality attributes (CQAs) using both screening and response surface designsbe able to design and analyze screening designs including a factorial, fractional factorial, and D-optimal designunderstand the need for adding center points to a designbe able to design and analyze response surface designs including central composite designs (CCDs), Box-Behnken designs, and I-optimal designspresent results of DOE studiesuse systematic understanding from DOE studies to update the control plan that is part of the overall risk management plan Who will benefit:This webinar is designed for pharmaceutical, biopharmaceutical, and medical device professionals who are involved with product and/or process design:Process Scientist/EngineerDesign EngineerProduct Development EngineerRegulatory/Compliance ProfessionalDesign Controls EngineerSix Sigma Green BeltSix Sigma Black BeltContinuous Improvement ManagerAgenda:Day 1 ScheduleLecture 1:Primer on Statistical Analysisbasic statisticstwo-sample t-testANOVAregressionLecture 2:Introduction to Design of Experiments (DOE)steps to DOEdefining critical quality attributes (CQAs)/responsesidentifying and prioritizing potential process parametersLecture 3:Screening Designsfull factorial designs2k factorial designsDay 2 ScheduleLecture 1:Screening Designs (continued)fractional factorial designsD-optimal designsLecture 2:Response Surface Designs2k factorial designs with center pointsCentral Composite Designs (CCDs)Box-Behnken designsI-optimal designsLecture 3:Utilizing Systematic Understanding from DOE Studiespresenting resultscontrol plan/risk management strategSpeaker: Jim WisnowskiJim Wisnowski 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.

He has over 25 years of experience and currently provides training and consulting services to industry and government in Design of Experiments (DOE), Reliability Engineering, Data Visualization, Predictive Analytics, and Text Mining. Dr. Wisnowski has been an invited speaker on applicability of statistics for national and international conferences. Prior to his current position, he was a senior program manager for URS, Chief of the Statistics Division in the Mathematics Department at the Air Force Academy, and a retired military officer.

He is currently a member of the editorial board of Quality Engineering and has published numerous international refereed journal articles on statistics. Jim has a PhD in Industrial Engineering from Arizona State University Location: Los Angeles, CA Date: March 30th & 31st, 2017 and Time: 9:00 AM to 6:00 PM Venue: Four Points by Sheraton Los Angeles International AirportAddress: 9750 Airport Boulevard, Los Angeles, CA, 90045, United States Price: Price: $1,295.00 (Seminar Fee for One Delegate)Until February 20, Early Bird Price: $1,295.00 from February 21 to March 28, Regular Price: $1,495.00Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)* Quick Contact:NetZealous DBA as GlobalCompliancePanel Phone: 1-800-447-9407Fax: 302-288-6884Email:


Four Points by Sheraton Los Angeles International Airport 9750 Airport Boulevard,
Los Angeles,
United States

Organizer Details

Conference organized by NetZealous DBA as GlobalCompliancePanel

NetZealous LLC-globalcompliancepanel, 161 Mission Falls Lane, Suite 216, Fremont,CA94539, USA
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