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USP 797 is  a standard established by the United States Pharmacopeia Convention (USP), a scientific non-profit organization dedicated to ensuring the quality of the American drug/ pharmaceutical supply, USP 797 also outlines the required procedures for compounding sterile drug preparations. 

If you’re considering designing and constructing a cleanroom, but aren’t exactly sure what ISO classifications are, you’ve come to the right place. Let’s air out some of the confusion. First of all, cleanrooms are classified by how pure the air is. Specifically, classifications are designed to categorize a cleanroom by the number of particles found in the lab’s air. The cleanroom classification standard ISO 14644- 1 uses particular particle count measurements to categorize the cleanliness or air purity level of a clean zone or cleanroom.

Question: Is an Iso class 5 clean room requirement the correct choice for my semiconductor work Answer: Yes, it just might be! It is correct that an ISO class 5 clean room is required for many semiconductor manufacturing processes. A typical semiconductor facility will have several different clean rooms, each with specific requirements to meet the needs of various manufacturing processes.

If you’re considering designing and constructing a cleanroom, but aren’t exactly sure what ISO classifications for cleanrooms are, you’ve come to the right place. Let’s air out some of the confusion. First of all, cleanrooms are classified by how pure the air is.  Specifically, classifications are...

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