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Demystifying Design of Experiments (DOE)
A Simple and Understandable Pathway to Using DOE
Conducted by Gamal Amer, Ph.D.
Principal - Premier Compliance Services, Inc.
June 20, 2014
This webinar will discuss the concepts associated with Design Of Experiments (DOE) or experimental design. Although DOE is a branch of statistics, this webinar will not address the statistical methods associated with the approach. Rather, the webinar will present an overview of the subject in simple and understandable language without encumbering the discussion with involved statistical discussion.
We will review the definition of DOE, its history and historical application and then review the application of DOE as part of developing responses to questions such as:
- What are the key factors in a process?
- What are the process settings that would deliver acceptable product quality with minimum variation?
- What are the interactions between the various variables associated with the process and their importance?
The presentation will discuss the concept associated with the Fisher methodology for DOE. These are comparison, randomization, replication, blocking, orthogonality, and factorial design. These concepts will be discussed individually in sufficient detail to give the uninitiated a feel for the capabilities and complexity of applying DOE in processes such as Process Validation. We will also present several examples detailing how to apply some of these concepts individually or in combination.
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All registrations include handout materials. Once you’re registered, you will receive via e-mail (the e-mail address you provide in your registration) the presentation handout materials the day before the seminar.
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Get the MP3 file and handout
GMP140620E - MP3 audio file and Handout materials
Gamal Amer, Ph.D.
Gamal Amer, Ph. D. is Principal at Premier Compliance Services, Inc.; Management Consultants for compliance and manufacturing operations performance in the life sciences industry. He holds a Ph. D. in Chemical Engineering and has over two decades experience in the Pharmaceutical and related industries. He has held positions of increased responsibility with leading pharmaceutical, consumer product and engineering consulting firms over the years. His experience includes comprehensive process design in bulk pharmaceutical manufacturing, biotechnology manufacturing, pharmaceutical solid dosage manufacturing and containment of potent and radioactive therapeutics. He is also experienced with facility development for therapeutic products operations.
Dr. Amer is a recognized expert in GMP compliance and validation. He has consulted for many of the leading pharmaceutical, biotechnology and medical device manufacturers. He has lectured extensively in the US, Europe, Asia and the Middle East, taught many courses, and authored many papers which were published in peer reviewed publication. He is a member of ISPE, PDA, ACS and AIChE.
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