A variety of our Wall Panels and Manufactured Buildings integrate with specialized equipment to offer temperature and humidity controlled rooms. Small or large enclosure and environmental control must meet stringent clean room requirements, such as ISO-ratings or clean room classifications and local building codes.

Upon inspection, you must know you can wash down and remove contaminates from your Modular Cleanroom Panels. InPlant’s Modular Building System of aluminum is non-corrosive, and the temperature and humidity controlled rooms handle the extremes. Your moisture-resistant manufactured buildings by InPlant can endure the rigorous cleanings and performance of its ISO-rating. 

InPlant will manufacture and prefabricate a Modular System to meet the clean room requirements of your laboratory, cleanroom, grow room, or any interior Cleanroom Panels and Modular Buildings to fulfill the needs of your business. Also, InPlant will assist with finding the appropriate Cleanroom Specialist to oversee the design, equipment, and installation through code certification and help you understand the Cleanroom Classifications of your project.

An Outline of Cleanroom Classifications

The US and Canada hold standard ratings of the ISO classification system ISO 14644-1. Federal Standards 209E (FS 209E) were in place before the current ISO ratings and rated by “classes,” which was replaced in 1999 by ISO-14644-1. The most current version of Cleanrooms and Associated Controlled Environments Standards is ISO 14644-1:2015, which was last reviewed and confirmed in 2021. 

Cleanroom Standards – ISO 14644-1:
ISO 1, ISO 2, ISO 3, ISO 4, ISO 5, ISO 6, ISO 7, ISO 8 and ISO 9
ISO 1 is the cleanest class, and ISO 9 is often cleaner than a regular room.
ISO ratings measure particle concentration for air cleanliness.

Federal Standards 209E:
Class 100,000, Class 10,000, Class 1,000, Class 100, Class 10, Class 1
These Classes also measure particle concentration for air cleanliness.
Class 1 is equivalent to ISO 3; Class 100,000 to ISO 8

Biosafety Levels:
BSL level P-1, P-2, P-3, and P-4
These cleanrooms use negative air pressure for production and medical research. BSL-1 labs study infectious agents or toxins but are not known to cause disease in healthy adults. BSL-4 labs study infectious agents or toxins that pose a high risk of infections and life-threatening diseases.

FDA & EU GMP (A-B-C-D): applies often in pharmaceutical manufacturing.
The European Union (EU) GMPs require a pharmaceutical quality system (PQS), along with a broad range of quality management. The US GMPs by the US Food and Drug Administration (FDA) help to establish a quality control unit (QCU) and the use of quality systems, but there are no specific requirements for a PQS. Airborne particles with sizes ≥ 5.0 μm have different EU and FDA requirements, among other differences in the FDA and EU standards are being reviewed to eliminate confusion.
• EU GMP Guidance Annex 1
• FDA: Current Good Manufacturing Practice (CGMP) regulations