Cleanrooms are determined by their level of cleanliness based on the particle counts in the environment. The ISO-14644-1 Standards range from ISO1(cleanest) to ISO9. The classifications are based on the 0.5micron size of particles per cubic meter and are maximum limits allowable in the air.
ISO1- xx
ISO2- 4
ISO3- 35 or Fed STD 209 Class1
ISO4- 352E or Fed STD 209 Class10
ISO5- 3,520 or Fed STD 209 Class100
ISO6- 35,200 or Fed STD 209 Class1,000
ISO7- 352,000 or Fed STD 209 Class10,000
ISO8- 3,520,000 or Fed STD 209 Class100,000
ISO9- 35,200,000
Cleanetics tests to meet ISO14644-1 standards and utilizes top testing equipment.
A cleanroom is not simply a room that gets cleaned. It is a carefully engineered environment designed to control particles, airflow, temperature, humidity, and pressure simultaneously. Every wall, seal, filter, and material choice plays a role in whether a facility passes certification or struggles with ongoing compliance. Understanding how cleanrooms are built helps facility managers, engineers, and operations teams make informed decisions that protect long-term performance. The process begins with detailed planning, where regulatory requirements, ISO classifications, product sensitivity, workflow design, equipment needs, and personnel movement patterns are evaluated. Mistakes at this stage are expensive to correct later and can limit performance for years if airflow design, layout, or system capacity are miscalculated.
At Cleanetics, we understand that a cleanroom is only as effective as the process behind it. From early planning to long-term maintenance, cleanrooms require precision, discipline, and expertise at every stage. Whether supporting pharmaceuticals, biotechnology, aerospace, or advanced manufacturing, Cleanetics partners with clients to ensure cleanroom environments meet strict performance and compliance standards — before, during, and after construction.
As we step into a new year, many organizations are setting goals for growth, efficiency, and innovation.
For companies in biotech, pharmaceutical manufacturing, medical device production, advanced
materials, and high-precision industries, a cleanroom isn’t just a part of the facility—it's the heart of
operations. And the new year is the perfect time to ensure that heart is performing at its best.
At Cleanetics, we believe that a cleanroom should evolve with the demands of your industry. Whether
you need an upgrade, a full-build custom solution, or an evaluation of your current environment, the
start of the year is the ideal moment to invest in a cleaner, safer, more compliant future.
Cleanrooms represent a significant investment, but without proper maintenance, they can quickly become liabilities. Preventive care is essential to protecting both financial and operational resources. **Reduced Downtime**: Malfunctioning systems can...
Building a cleanroom is a complex project that involves design, engineering, construction, and compliance. A turnkey solution simplifies the process by providing a single point of accountability. With turnkey construction, Cleanetics manages every...
At Cleanetics, we design, build, certify, and maintain cleanrooms that meet the highest industry standards. Our team supports healthcare, pharmaceuticals, biotechnology, and advanced manufacturing by delivering safe, compliant, and reliable environments.
At Cleanetics, we understand that a cleanroom is more than just a controlled space—it’s the heart of critical work in healthcare, pharmaceuticals, research, and advanced manufacturing.
We are always adding new features and updating our content to bring you the most up to date information about our company. Check back often for updates.
