High-Quality USP 800 Clean Room Construction
Cleanroom Logic provides high-quality USP 800 clean room construction for many industries, including pharmaceutical, healthcare, and other industries. USP 800 clean room construction depends upon constructing a cleanroom that adheres to USP 800 standards, namely that the room is capable of containing both sterile and non-sterile hazardous materials. Trust Cleanroom Logic to properly construct, install, and enclose this cleanroom to ensure it can properly handle and contain both non-sterile and sterile hazardous materials.
What is a USP 800 Cleanroom?
A USP 800 cleanroom is a cleanroom that adheres to USP 800 standards set by the United States Pharmacopoeia (USP) to ensure that hazardous drugs are properly handled and contained throughout its many stages from delivery to storage to administration. A USP 800 cleanroom is designed to properly contain hazardous medicines used in such medical procedures and practices as chemotherapy, bioengineered drugs, immunosuppressants, hormone therapies, and more. USP 800 guidelines and the corresponding cleanroom are designed to protect patients, healthcare workers, and the environment from exposure to these hazardous medicines and materials.
How is a USP 800 Clean Room Designed?
In order to design a USP 800 clean room, all materials and surfaces within must be non-shedding, non-porous, and smooth. Hazardous materials cannot be allowed to accumulate within walls or hard-to-reach areas. There should be sufficient lighting to ensure for safe operations within the USP 800 clean room, and noise should be minimized to ensure the environment is both comfortable and safe. In addition, high-efficiency particulate air (HEPA) filters must be present to ensure airflow within this clean room is controlled to prevent the spreading of dangerous particles.
Contact us to learn more about our experienced team and how they can help to build your custom cleanroom and fulfill your specific requirements.