Design of Experiments (DOE) is an important technique for root cause analysis (RCA) and process improvement. As an example, when potential trouble sources are identified from a cause and effect diagram, DOE can be used to determine which of the factors are likely to be important. DOE can also develop quantitative models of the nature y=f(x) (y is a function of x) where y is often a critical quality characteristic.
WHY SHOULD YOU ATTEND?
While DOE is normally a subject for full-length college courses, the basics can be covered in a one-hour webinar. These fundamentals include hypothesis testing, which also carries over into acceptance sampling and statistical process control, as well as the design of the experiment to exclude extraneous variation sources (randomization and blocking techniques).
AREA COVERED
- Value of DOE in the language of time and money, as shown by comparison of an experiment performed by Frederick Winslow Taylor during the late 19th century, and an even more complicated one performed by a pharmaceutical company that sought FDA approval for a diagnostic test
- Hypothesis testing is the foundation of most industrial statistics applications including not only DOE but also statistical process control and acceptance sampling (e.g. ANSI/ASQ Z1.4 and ANSI/ASQ Z1.9)
- Interactions, or situations in which the whole is greater or less than the sum of its parts. Interactions cannot be detected by one variable at a time experimentation.
- Experimental design considerations include randomization, blocking, and replication.
- This webinar will provide a sufficient foundation for attendees to work effectively with industrial statisticians, Six Sigma Green and Black Belts, and similar subject matter experts.
LEARNING OBJECTIVES
Attendees will learn the fundamentals of DOE, some of which carry over into other industrial statistics applications such as acceptance sampling and statistical process control.
- Hypothesis testing is the foundation of almost everything we do with industrial statistics.
- The null hypothesis, or starting assumption, is that there is no difference between the experiment and the control, a production lot is acceptable, or a process is in control.
- The alternate hypothesis is that the experiment differs from the control (is better than the control in an improvement activity), a production lot should be rejected, or a process is out of control and needs adjustment.
- We must prove the alternate hypothesis beyond a quantitative reasonable doubt that is known as the Type I risk, alpha risk, or, in acceptance sampling, the producer’s risk (of wrongly rejecting an acceptable lot).
- DOE can save an enormous amount of time and money, as shown by a comparison of an experiment performed in the late 19th century (prior to the development of industrial statistics) and an even more complex one performed roughly 100 years later. This underscores the value of DOE in the language of money, i.e. the language of upper management.
- Understand the concepts of factors, levels, and interactions (the whole is greater or less than the sum of its parts). Factors such as machine or material are often identified from a cause and effect diagram during root cause analysis.
- Recognize the need to exclude extraneous variation sources from the experiment through randomization and blocking, and also the need to use a sufficiently large sample to get meaningful results (replication).
- Explain the results of an experiment in terms of its significance level or P value(the chance that the observed results are due to random chance).
WHO WILL BENEFIT?
- Manufacturing Departments
- Lab Supervisors and Managers
- Quality Departments
- Quality Technicians
While DOE is normally a subject for full-length college courses, the basics can be covered in a one-hour webinar. These fundamentals include hypothesis testing, which also carries over into acceptance sampling and statistical process control, as well as the design of the experiment to exclude extraneous variation sources (randomization and blocking techniques).
- Value of DOE in the language of time and money, as shown by comparison of an experiment performed by Frederick Winslow Taylor during the late 19th century, and an even more complicated one performed by a pharmaceutical company that sought FDA approval for a diagnostic test
- Hypothesis testing is the foundation of most industrial statistics applications including not only DOE but also statistical process control and acceptance sampling (e.g. ANSI/ASQ Z1.4 and ANSI/ASQ Z1.9)
- Interactions, or situations in which the whole is greater or less than the sum of its parts. Interactions cannot be detected by one variable at a time experimentation.
- Experimental design considerations include randomization, blocking, and replication.
- This webinar will provide a sufficient foundation for attendees to work effectively with industrial statisticians, Six Sigma Green and Black Belts, and similar subject matter experts.
Attendees will learn the fundamentals of DOE, some of which carry over into other industrial statistics applications such as acceptance sampling and statistical process control.
- Hypothesis testing is the foundation of almost everything we do with industrial statistics.
- The null hypothesis, or starting assumption, is that there is no difference between the experiment and the control, a production lot is acceptable, or a process is in control.
- The alternate hypothesis is that the experiment differs from the control (is better than the control in an improvement activity), a production lot should be rejected, or a process is out of control and needs adjustment.
- We must prove the alternate hypothesis beyond a quantitative reasonable doubt that is known as the Type I risk, alpha risk, or, in acceptance sampling, the producer’s risk (of wrongly rejecting an acceptable lot).
- DOE can save an enormous amount of time and money, as shown by a comparison of an experiment performed in the late 19th century (prior to the development of industrial statistics) and an even more complex one performed roughly 100 years later. This underscores the value of DOE in the language of money, i.e. the language of upper management.
- Understand the concepts of factors, levels, and interactions (the whole is greater or less than the sum of its parts). Factors such as machine or material are often identified from a cause and effect diagram during root cause analysis.
- Recognize the need to exclude extraneous variation sources from the experiment through randomization and blocking, and also the need to use a sufficiently large sample to get meaningful results (replication).
- Explain the results of an experiment in terms of its significance level or P value(the chance that the observed results are due to random chance).
- Manufacturing Departments
- Lab Supervisors and Managers
- Quality Departments
- Quality Technicians
Speaker Profile

William A. Levinson, P.E., is the principal of Levinson Productivity Systems, P.C. He is an ASQ Fellow, Certified Quality Engineer, Quality Auditor, Quality Manager, Reliability Engineer, and Six Sigma Black Belt. He is also the author of several books on quality, productivity, and management, of which the most recent is The Expanded and Annotated My Life and Work: Henry Ford’s Universal Code for World-Class Success.
Upcoming Webinars

Contractor vs Employee: How to Tell the Difference and What…

Imposter Syndrome: How to Define, Understand & Shift Your E…

FDA current recommendations related to timely initiation of…


Impact Assessments For Supplier Change Notices

Implicit Bias: Becoming Aware of Your Inner Storyteller

Complying with the NEW I-9 and E-Verify Regulations - The I…

The Federal Anti-Kickback Statute & Stark Law: What Physici…

Building an Effective Injury Management Process

Fatal Errors Employers Make When Updating Employee Handbook…

Understanding the Changes Coming to NCCI's Experience Mod i…

From Awareness to Action: Going Beyond the Law in Preventin…

Onboarding is NOT Orientation - How to Improve the New Empl…


From Awareness to Action: Going Beyond the Law in Preventin…


FDA Compliance and Clinical Trial Computer System Validation

5 Proven Ways To Engage & Retain Your Team Even During The …


Customer Relationship Management: Strategic Methods to Mana…

Navigating New Paths: Unveiling Your Unique Abilities for a…

Form 1099 Update 2023: Latest Forms, Rules and Reporting Re…

Strategic Interviewing & Selection: Getting the Right Talen…



Project Management for Non-Project Managers - How to Effect…

Implementing a Robust Change Control Program - Key Elements…

Amazing (!) AI Tools For Building Your Business



Excel - Unleashing the Full Potential of New Functions (Exc…

How to Conduct Annual Product Reviews to Achieve GMP Compli…



What Business Leaders Need to Know About Cybersecurity Prep…

Responding to EEOC Discrimination Charges-What's Your Busin…

Harassment, Bullying, Gossip, Confrontational and Disruptiv…