What Equipment is Actually Required for a USP 797 Compliant Cleanroom?
USP 797 compliance is a federal standard for healthcare facilities and is subject to regulatory oversight. If you’re setting up or auditing a pharmacy compounding cleanroom,…
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ISO Cleanroom Standards Explained: ISO Classes 1–9
Understanding ISO cleanroom classifications is essential when specifying, designing, or evaluating controlled environments. Classifications such as ISO 7 and ISO 8 directly impact product quality, regulatory…
Cleanroom Airlocks vs Cleanroom Air Showers
In specialized manufacturing, semiconductor, pharmaceutical, medical, or food and beverage production facilities, cleanrooms maintain contaminant-free, temperature- and humidity-controlled conditions for sensitive items and processes. As workers…
Our HOMAG Automation Cleanroom Featured on Thomasnet.com
We recently updated our cleanroom equipment manufacturing process by purchasing a new Homag CENTATEQ P-110 Series, used to automate the manufacturing of laminar flow benches. Learn…
HEPA vs. ULPA Filters
Depending on your cleanroom setup and filtration needs, you can opt for either a HEPA or ULPA filter. Knowing the differences between ULPA vs. HEPA filters…
Cleanroom Certification for Critical Manufacturing
Items including semiconductors, pharmaceuticals, medical devices, aerospace components, and others are easily damaged or compromised by dust, dirt, and temperature or humidity fluctuations. These highly sensitive…
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