Markets

Pharmaceutical facilities must adhere to strict ISO standards and industry guidelines to ensure process contamination is controlled to the highest of standards. These include ISO 14644-1, outlining particulate control, USA FDA Aseptic Guidance, cGMP, and ISPE Good Practices.

Data Centers focus on the control of airflow and particulate matter. This can be achieved by applying fluid dynamics in addition to installing Hot Aisle Containment or Cold Aisle Containment systems.

Defense and Aerospace cleanrooms are constructed to control environmental contamination in the precision manufacturing of critical hardware, electronics, and other sensitive equipment. These cleanrooms are typically constructed as non-outgassing, with electro-static discharge materials, silicone-free, and follow ISO 14644 standards.

Battery Facilities focus on the control of particulate matter, humidity, and temperature. These cleanrooms follow ISO 14644-1 standards outlining particulate matter parameters, in addition to dry room relative humidity standards.

These facilities are critical in the development of life saving treatments and therapies. Standards and industry guidelines can include ISO 14644, ASME BPE, and USA FDA Aseptic Guidance in addition to many others.

Semiconductor facilities require a stringent cleanroom design to achieve and maintain strict cleanliness standards without hindering process and workflow. These cleanrooms typically comply with ISO 14644, ASTM standards and NASA Standards.

Medical Device manufacturing processes are held to ISO 14644 standards to control particulate matter and contamination of potentially life saving equipment.

Research laboratory requirements can vary based on the industry being served. Typically these control measures are centered around particulate matter, microbes, ESD, and others.  These facilities are constructed to be a sterile environment with controlled environmental interference.

Food and Beverage facilities are considered a controlled environment, in which cleanliness and processes follow strict standards and industry guidelines. These can include ISO 22000, food safety management, cGMP, and FDA 21 CFR, in addition to others.