In Michigan, ensuring air quality and compliance goes beyond meeting industry standards, it’s about protecting the people, processes, and products that depend on clean, controlled environments. With over 20 years of expertise, Class 1 Air provides tailored air quality solutions for businesses across the state, from healthcare facilities to pharmaceutical manufacturing and research labs.
Our comprehensive services include cleanroom testing, fume hood testing, and isolator testing, ensuring high industry standards. We partner with prestigious institutions for training, including the Eagleson Institute, CETA, NEBB, Harvard School of Public Health, CDC, NIH, and others, providing our technicians with the latest knowledge and skills.
What sets us apart is being an expert single-source provider, we handle everything from certification and testing to maintenance and repairs, ensuring a seamless experience for our clients. Our efficient reporting processes mean you receive cleanroom reports in as little as 2 weeks and same-day results for biosafety cabinets and hoods, helping you maintain uninterrupted operations.
We provide reliable services designed to meet your unique needs. Contact us today to learn more and receive a free quote!
Following the test procedures implemented by USP in CETA CAG 003 2006, our CETA National Board of Testing(CNBT) accredited technicians provide the expertise needed to keep you compliant and up to date on the latest standards from USP .
BioSafety Cabinets (BSCs) are an essential safety devices found in your laboratory or pharmacy. Following NSF standard 49 annex F, we certify any type of BSC. Protecting your environment, personnel and your product; a properly functioning BSC is indispensable
Cleanrooms play a critical role in maintaining a contamination free process and end product. Class 1 Air can perform complete cleanroom performance testing following international standards to meet and maintain your ISO-14644 classification. Room pressure
Our state of the art ISO microbiology labs can provide end-to-end management of your microbiological samples.
Validation is the process of establishing evidence demonstrating that your process maintains the desired level of compliance at all stages. This can be applied to a facility, a cleanroom, or a process. We have experience writing and executing
Compressed air is used in greater than 70 percent of manufacturing applications, including pharmaceutical, food and beverage, and medical device manufacturing. We can provide you with the peace of mind that your compressed air system passes the tests
Keep your personnel and the environment safe from powders. Inside these enclosures, delicate powders from your weigh stations are captured by a HEPA filter. These enclosures are the first defense in keeping your product contained. Use in non-sterile compounding