Why clean the room? It’s a cleanroom, isn’t it? This was the most popular question when we began cleaning cleanrooms in 1980. Owners and operators often assumed that because their cleanrooms were equipped with state-of-the-art air filtration systems and other safeguards, normal cleaning procedures were optional or even unnecessary.
Modular CMM enclosures are used to provide a controlled environment for your coordinate measuring machines. Using your equipment inside a CMM room protects it from environmental factors and allows your machine to provide X, Y, and Z coordinates with increased accuracy.
Flooring can be at the bottom of the ladder when planning a new cleanroom. As contamination has a downward flow it is an element not often given as much consideration as those featuring higher in the cleanroom; wall construction, for example. But, a non-cleanroom compliant floor could introduce and harbour contamination to the environment thus putting manufacturing processes at risk.
“The choices and the technology out there in the market are growing,” says Rebecca Smith, national territories manager at Connect 2 Cleanrooms. Smith believes it is important to consider flooring right at the beginning of the cleanroom planning stage, so the correct type is selected. She points out that considerations including GMP requirements, the existing flooring, process compatibility, cleaning protocol and cleanroom type will drive the selection decision.
There are two main cleanroom flooring options, namely loose lay flooring and vinyl flooring. Each has many variants, bringing its own benefits and opportunities. Smith comments: “Both types are available in multiple colours, meaning areas can be colour coded to signal separate zones within the cleanroom, or pathways can be created to signpost operatives.”
Windows are among the most essential parts of a well-maintained cleanroom. Here are tips for cleaning windows in your cleanroom.
A cleanroom is a controlled environment where products are packed, manufactured, and assembled. The room eliminates sub-micron airborne contamination generated from people, processes, facilities and equipment. The higher the level of cleanliness, the lower the likeliness of particles or microbes damaging or corrupting production processes by tainting sterile and non-sterile products.
Clean Rooms are workplaces where contamination is controlled. The Clean Rooms are said to provide a conducive environment (for research, development and manufacturing of equipment or processes) with a low level of environmental pollutants such as dust, airborne microbes, aerosol particles, and chemical vapors.
A clean room is a controlled work area that maintains a specified level of air particulates and other contaminants. Clean rooms are common in many industries, such as pharmaceuticals, medical device manufacturing, scientific research, chemical processing, and electronics manufacturing. Clean room design requires careful consideration of its intended use, permissible particle concentration, location, manufacturing process, and cost. The design and specification of a clean room require close coordination between the design team and all of the departments or parties that will use the room.
In most large-scale FDA-regulated pharmaceutical manufacturing operations, it is required that the product be manufactured in a clean room classified between Class 100 and Class 100,000. In an operation where medical tubing is being extruded, the classification would likely be Class 100,000. In a process where inject-able drugs are being manufactured, the classification would most likely be Class 100 or Class 1000.
Cleanrooms and their controlled environments have long been associated with the pharmaceutical and medical industries, but thousands of jobs in cleanrooms have been created in other industries where practitioners perform some amazing applications and experiments within the cleanroom setting. Because the cleanroom can be designed to precision specifications and may operate in accordance with strict industry practices, their clean environment lends itself to many manufacturing pursuits that depend upon its enhanced quality controls. The following are just a few of the amazing applications that cleanroom technology fosters.
Clean rooms are “created” when clean room designers like Vernick & Associates bring together engineering design, fabrication, finish, and operational controls to convert a “normal” room to a “clean room” so that they can be used for manufacturing. These clean rooms must meet the requirements defined in the Sterile Code of Annex 1 of both the EU and PIC/S Guides to GMP and other standards and guidance as required by local health authorities.
 |
 |
 |
 |
 |
 |
 |
 |
 |