Content By Bruce McDuffee

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By: Bruce McDuffee

Quality of compressed air is a broad term. One person may deem his compressed air quality as “poor” if he finds water at the end-use point. Another may tell you that her compressed air is high quality because she is able to maintain a dew point temperature at –40°F or lower. As with any measurement, in order to be consistent, we must have a reference for comparison. In the world of compressed air, the most common reference is ISO 8573.1.

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By: Bruce McDuffee

Humidity is a tough measurement. It’s very hard to get a repeatable measurement with low uncertainty. This post discusses seven best practices that will help you make a more accurate, repeatable, and reliable humidity measurement. The recommendations are primarily based on the NPL document, “A Guide to the Measurement of Humidity.” 

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By: Bruce McDuffee

Ask any metrologist, and you’ll likely get quite a diatribe about the challenge of making a good measurement of humidity. There are, however, some specific steps or best practices you can follow that will help improve your measurement of humidity through better accuracy, better repeatability, and fewer errors.

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By: Bruce McDuffee

Please tell me how to map this chamber!” This is a plea we hear at every Vaisala current Good Manufacturing Practice (cGMP) seminar. The question deals with environmentally controlled chambers, everything from small refrigerators or freezers, to walk-in chambers or even large warehouses regulated under cGMP rules and guidelines. Attendees who ask the question are usually more interested in how to map a chamber for maximum reliability or effectiveness as opposed to meeting the U.S.

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By: Bruce McDuffee

If you’re in the business of manufacturing drugs, medical devices, nutraceuticals, or manufacturing or importing any product in the United States that falls under current Good Manufacturing Processes (cGMP) regulations, your facility will be inspected by the U.S. Food and Drug Administration (FDA).

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