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Phone: 1 (800) 962-3058
E-Mail: sales@alliedcleanrooms.com

California - CSLB #730592B
GSA Contract # 47QSWA19D0062

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27 Jan

Posted at 22:28h in Blog by

Introduction

It's a fact: the cleanroom industry is booming. Whether you're a large corporation or small startup, if you have any kind of manufacturing facility or laboratory—and especially if you work with high-risk or fragile materials—then having a cleanroom can be essential to success. But knowing how much space and how many worksurfaces to include in your new modular cleanroom? That's where things get complicated. It's not as simple as just looking at square footage and thinking about what might go on inside your new space. You'll also need to consider your budget, the volume of traffic that will come through every day (if any), whether there are any special requirements for humidity levels or temperature control, and plenty more factors besides!

24 Dec

Posted at 21:41h in Blog by
So-called "hard construction" has many apparent advantages. Business owners often like the idea of "custom" construction, but "custom" can be less than it appears. On the other hand, modular construction might seem "rigid," but that is not the case. Ironically, modular construction including modular cleanroom construction can have impressive advantages that outweigh those of "hard construction." Let's investigate.

21 Dec

Posted at 21:37h in Blog by
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. 

21 Oct

Posted at 20:40h in Blog by
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.

17 Oct

Posted at 20:25h in Blog by
Modular cleanrooms provide many plusses when it comes to the design, installation, and even maintenance of cleanroom. Let's explore how and why. First, when you're renting a building, you don't own it. And when you're done with your lease, you have to return the building exactly as you received it — if not better. Renting, quite frankly, isn't as good as owning.

01 Oct

Posted at 16:45h in Blog by
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.

22 Sep

Posted at 23:13h in Blog by

Introduction

It's a fact: the cleanroom industry is booming. Whether you're a large corporation or small startup, if you have any kind of manufacturing facility or laboratory—and especially if you work with high-risk or fragile materials—then having a cleanroom can be essential to success. But knowing how much space and how many worksurfaces to include in your new modular cleanroom? That's where things get complicated. It's not as simple as just looking at square footage and thinking about what might go on inside your new space. You'll also need to consider your budget, the volume of traffic that will come through every day (if any), whether there are any special requirements for humidity levels or temperature control, and plenty more factors besides!

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