Displaying items by tag: cleaning

ISO-7 cleanroom classification is a common medium level of the cleanroom classes. The ISO cleanroom standards are set by the International Organization for Standardization (https://www.iso.org/standards.html). They are a private international organization with a membership of 167 national standards bodies. The ISO cleanroom classification system used in the United States is primarily for pharmaceutical cleanrooms, medical device cleanrooms, biotech cleanrooms, life-science cleanrooms, and  USP797/800 compounding cleanrooms. Europe and the rest of world uses the ISO cleanroom classification system for all industries except semiconductor.

In accordance with the ISO 14644 standards, ISO Class 7 cleanrooms represent a highly controlled environment that is engineered to maintain specific cleanliness values. The enclosed system encompasses ceiling-mounted fan filter units (FFUs) that generate a continuous supply of HEPA or ULPA-filtered air. In this article, we'll cover top-level considerations and standards for ISO 7 cleanroom design and construction. Additionally, we'll explore general principles for ISO 7 standards including particulate levels, ACH requirements, and equipment-based considerations among several unique applications.

Maintaining a compliant cleanroom is vitally important. CLIN, a leading manufacturer of cleaning and disinfection supplies, is committed to partnering with customers in various industries such as pharmaceutical manufacturing, biotechnology, and ATMP manufacturing.

I have to admit, I’ve also been confused about the cleaning protocols and procedures for a cleanroom environment. The basic techniques, I’ve got that down (but I’ll talk about that too); there’s a lot of products to clean with and rotating your cleaning agents. It’s confusing to say the least and the internet is vast and for something so important how do you trust the information (since you are reading this online – myself included!)? I’ll share my references and you can see where I’m getting this information on clean room protocol. I’ve found a source that not only knows what they’re talking about and have the proper credentials but also speaks on a practical level that makes sense to me. I’ll try to be as concise as possible in explaining this because you’ll see the basics don’t necessarily warrant an hour long discussion.

When you operate a cleanroom, it's imperative to maintain strict standards of cleanliness in the facility at all times. Whether you work in healthcare, biotechnology, pharmaceuticals, aerospace, or any other setting where cleanrooms are employed, a rigorous cleaning protocol is vital.

After investing in a top-of-the-line cleanroom, keeping it in pristine condition is crucial. When properly cared for, a cleanroom will function at peak performance. If not, the quality of the cleanroom can quickly deteriorate, affecting daily operations.

Floors and walls have large surface areas and must therefore need wiping cloths and techniques designed for thorough sterilisation.

Finally, your clean room is installed and fully operational. You put a lot of time and resources into creating your perfect cleanroom. Now you can sit back and relax.

Contamination sources that find their way into your cleanroom can be broadly classified into two categories. Those originating from the physical plant and those from processes/human actions.

Cleanrooms are a crucial part of specialized industries like pharmaceutical production, tech manufacturing, and biological research. Specialized equipment and stringent procedures minimize contaminants, direct airflow, and help protect sensitive business operations and the people they serve.