Cleanroom Testing & Different Industries

Cleanroom Testing & Different Industries

Providing Cleanroom Testing For Different for Industries

There are many different types of industries that use cleanrooms, so what makes a cleanroom in one industry different than another? It’s quite a common question. Let’s have a look at the different cleanroom industries in more detail along with varying ISO requirements.

Biotechnology and Pharmaceutical Cleanroom TestingBiotechnology and Pharmaceutical Cleanroom Testing
Many biotechnology and pharmaceutical cleanrooms are specified at ISO Class 5 to ISO Class 8 and apply to a large portion of the cleanroom standards. If you’re not familiar, ISO classes and standards are set by the International Organisation for Standardisation.

The many ISO standards provide various requirements, specifications, guidelines and characteristics that can be used consistently to ensure that materials, products, processes and services are fit for their intended purpose.

In all cleanrooms, particulate matter is a great concern. Specifically, viable particulate contamination should receive careful consideration and attention. Viable particulate contamination refers to the ability to keep the room clean by typically using modular or stick-built components with integral cove bases and corners, as well as coved ceilings in order to maintain a cleanable surface condition. This high grade finish is crucial for biotechnology and pharmaceutical cleanroom standards.

In all instances concealed areas may allow for bacterial growth which is unacceptable. These clean rooms typically use cleanroom technology that keeps the seal unbroken during sanitation and filter changes. Biotechnology and pharmaceutical cleanrooms typically have a heavy focus on pressurisation control, the elimination of cross contamination and the on-going filtration of outdoor air and indoor air.

Defence Industry Cleanroom Testing Defence Industry Cleanroom Testing
The defence and optic industries use cleanrooms for many of their applications, including biotech, pharmaceutical, and medical device. These applications may also include items such as like chip making for controlling missiles and electronic and radar components, laser technology for guidance systems and even biological components for vaccines etc.

Defence Industry Cleanrooms usually require the highest levels of security and clearance. Due to the sensitive/high security nature of various defence industry operations, this typically leads to the stick-built type of construction to allow for the perimeter to meet government security requirements.

Medical Device Cleanroom Testing
Cleanrooms for medical device technology typically fall under ISO Class 7 and ISO Class 8 range. As you can imagine the manufacturing process for these products ensures that the surface of the product does not have particulate contamination when it is completed. So, it is imperative that the cleanliness level inside the room is maintained both from a cleanroom standpoint.

In many cases people/personal is the major contaminator in most processes. This is why personnel are required to wear full gowns, booties, gloves, and hairnets in medical device manufacturing, as well as the biotech, pharmaceutical and semiconductor industries. While some medical device cleanrooms may not always adhere to the same stringent gowning practices as pharmaceutical cleanrooms, the protocol and cleaning process is just as important. The cleanroom environment for medical devices usually aims to eliminate surface contamination, or viable particulate, on their products.

Medical Device Cleanroom TestingMicroelectronic and Nanotech Cleanroom Testing
Microelectronic and Nanotech Cleanrooms are designed to maintain temperature, humidity, particulate, static and pressure levels. This is due to the fact that these factors, as well as static forces, can easily affect or compromise the final product, taking into account the huge costs associated with these types of works there’s simply no room for error.

A high level of cleanliness must be maintained at all times within nanotech and microelectronic cleanroom environments since defects can occur at any stage in this process. Many steps are involved in order to come to a final product, and a defect along the way might not be discovered until the very end. Most of these cleanrooms typically operate in a cleanroom classification range from ISO Class 1 to ISO Class 6 with various processes occurring at different levels of cleanliness.

Microelectronic and Nanotech Cleanroom TestingAutomotive Cleanroom Testing
Since the early invention of the assembly line, the automotive industry has made incredible strides in their manufacturing processes. Indeed, a wide range of attention is given to mass defects, or preventing them. Like other industries the need for manufacturing auto components inside cleanrooms has become a key factor in the automotive industry. .

In Automotive Cleanrooms factors like pressure, temperature and humidity are just as important to other rooms designed in the cleanroom classification range of ISO 7 and ISO 8. The defects that can (and do) occur in the automotive manufacturing industry are vast, including costly errors like glass coatings, electrical components, and painting to the bodywork.

Automotive Cleanroom Testing APT Cleanroom Testing Has Your Industry Covered
I hope the above information was informative. If you would like some more information in regards to our cleanroom testing service please don’t hesitate to contact Darren directly on 07775623464.

APT Cleanroom Testing provides clients with a reliable and proactive clean room testing service. If you would like to know more about our particulate testing service and/or HEPA filter testing service to cleanrooms, please don’t hesitate to contact us at: info@airpressuretesting.net


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