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DOE

Blog posts and articles about the statistical method called DOE (Design of Experiments) in quality improvement.

One of the biggest pieces of international news last year was the so-called "Brexit" referendum, in which a majority of voters in the United Kingdom cast their ballots to leave the European Union (EU). That outcome shocked the world. Follow-up media coverage has asserted that the younger generation prefers to remain in the EU since that means more opportunities on the continent. The older... Continue Reading
For a process improvement practitioner, finishing the Control Phase of the DMAIC process is your ticket to move on to your next project. You’ve done an excellent job leading the project team because they identified root causes, developed and implemented solutions to resolve those root causes, put a control plan in place and transitioned the process back to the Process Owner. Soon, however, you... Continue Reading

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If you have a process that isn’t meeting specifications, using Monte Carlo simulation and optimization can help. Companion by Minitab offers a powerful, easy-to-use tool for Monte Carlo simulation and optimization, and in this blog we'll look at the case of product engineers involved in steel production for automobile parts, and how they could use Companion to improve a process. The tensile... Continue Reading
It's a very exciting time at Minitab's offices around the world because we've just announced the availability of Minitab® 18 Statistical Software. Data is everywhere today, but to use it to make sound, strategic business decisions, you need to have tools that turn that data into knowledge and insights. We've designed Minitab 18 to do exactly that.  We've incorporated a lot of new features, made some... Continue Reading
The 1949 film A Connecticut Yankee in King Arthur's Court includes the song “Busy Doing Nothing,” and this could be written about the Null Hypothesis as it is used in statistical analyses.  The words to the song go: We're busy doin' nothin'Workin' the whole day through Tryin' to find lots of things not to do And that summarises the role of the Null Hypothesis perfectly. Let me explain why. What's... Continue Reading
Rare events inherently occur in all kinds of processes. In hospitals, there are medication errors, infections, patient falls, ventilator-associated pneumonias, and other rare, adverse events that cause prolonged hospital stays and increase healthcare costs.  But rare events happen in many other contexts, too. Software developers may need to track errors in lines of programming code, or a quality... Continue Reading
For the majority of my career, I've had the opportunity to speak at conferences and other events somewhat regularly. I thought some of my talks were pretty good, and some were not so good (based on ratings, my audiences didn't always agree with either—but that's a topic for another post). But I would guess that well over 90% of the time, my proposals were accepted to be presented at the... Continue Reading
by Matthew Barsalou, guest blogger For want of a nail the shoe was lost,For want of a shoe the horse was lost,For want of a horse the rider was lostFor want of a rider the battle was lostFor want of a battle the kingdom was lostAnd all for the want of a horseshoe nail. (Lowe, 1980, 50) According to the old nursery rhyme, "For Want of a Nail," an entire kingdom was lost because of the lack of one... Continue Reading
As someone who has collected and analyzed real data for a living, the idea of using simulated data for a Monte Carlo simulation sounds a bit odd. How can you improve a real product with simulated data? In this post, I’ll help you understand the methods behind Monte Carlo simulation and walk you through a simulation example using Companion by Minitab. Companion by Minitab is a software platform that... Continue Reading
Have you ever tried to install ventilated shelving in a closet?  You know: the heavy-duty, white- or gray-colored vinyl-coated wire shelving? The one that allows you to get organized, more efficient with space, and is strong and maintenance-free? Yep, that’s the one. Did I mention this stuff is strong?  As in, really hard to cut?  It seems like a simple 4-step project. Measure the closet, go the... Continue Reading
Grocery shopping. For some, it's the most dreaded household activity. For others, it's fun, or perhaps just a “necessary evil.” Personally, I enjoy it! My co-worker, Ginger, a content manager here at Minitab, opened my eyes to something that made me love grocery shopping even more: she shared the data behind her family’s shopping trips. Being something of a data nerd, I really geeked out over the... Continue Reading
If you regularly perform regression analysis, you know that R2 is a statistic used to evaluate the fit of your model. You may even know the standard definition of R2: the percentage of variation in the response that is explained by the model. Fair enough. With Minitab Statistical Software doing all the heavy lifting to calculate your R2 values, that may be all you ever need to know. But if you’re... Continue Reading
In Parts 1 and 2 of Gauging Gage we looked at the numbers of parts, operators, and replicates used in a Gage R&R Study and how accurately we could estimate %Contribution based on the choice for each.  In doing so, I hoped to provide you with valuable and interesting information, but mostly I hoped to make you like me.  I mean like me so much that if I told you that you were doing... Continue Reading
Earlier, I wrote about the different types of data statisticians typically encounter. In this post, we're going to look at why, when given a choice in the matter, we prefer to analyze continuous data rather than categorical/attribute or discrete data.  As a reminder, when we assign something to a group or give it a name, we have created attribute or categorical data.  If we count something, like... Continue Reading
You run a capability analysis and your Cpk is bad. Now what? First, let’s start by defining what “bad” is. In simple terms, the smaller the Cpk, the more defects you have. So the larger your Cpk is, the better. Many practitioners use a Cpk of 1.33 as the gold standard, so we’ll treat that as the gold standard here, too. Suppose we collect some data and run a capability analysis using Minitab Statisti... Continue Reading
by Kevin Clay, guest blogger In transactional or service processes, we often deal with lead-time data, and usually that data does not follow the normal distribution. Consider a Lean Six Sigma project to reduce the lead time required to install an information technology solution at a customer site. It should take no more than 30 days—working 10 hours per day Monday–Friday—to complete, test and... Continue Reading
"You take 10 parts and have 3 operators measure each 2 times." This standard approach to a Gage R&R experiment is so common, so accepted, so ubiquitous that few people ever question whether it is effective.  Obviously one could look at whether 3 is an adequate number of operators or 2 an adequate number of replicates, but in this first of a series of posts about "Gauging Gage," I want to look at... Continue Reading
In Part 1 of this blog series, I compared Six Sigma to a diamond because both are valuable, have many facets and have withstood the test of time. I also explained how the term “Six Sigma” can be used to summarize a variety of concepts, including philosophy, tools, methodology, or metrics. In this post, I’ll explain short/long-term variation and between/within-subgroup variation and how they help... Continue Reading
In my last post, I wrote about making a cluttered data set easier to work with by removing unneeded columns entirely, and by displaying just those columns you want to work with now. But too much unneeded data isn't always the problem. What can you do when someone gives you data that isn't organized the way you need it to be?   That happens for a variety of reasons, but most often it's because the... Continue Reading
In its industry guidance to companies that manufacture drugs and biological products for people and animals, the Food and Drug Administration (FDA) recommends three stages for process validation: Process Design, Process Qualification, and Continued Process Verification. In this post, we we will focus on that third stage. Stage 3: Continued Process Verification Per the FDA guidelines, the goal of... Continue Reading