Pharmaceutical compounding cleanrooms provide an essential environment for the processing of sterile and non-sterile drugs. This CleanPro® modular sterile compounding cleanroom is designed for USP 797 and USP 800 compliance for compounding chemotherapy drugs. Safe handling of sterile compounds requires special considerations, including heat-welded floors, anterooms, and buffer areas.
For this customer, CleanPro® also sourced and provided furniture and equipment for the cleanroom and anteroom, including clean tables, seating, storage, and waste receptacles.
If you find yourself overwhelmed in a jungle of acronyms, terminology, and technical cleanroom specs, there might be a better way. CleanPro® helps you achieve the correct pressurization differentials, ACPH and ISO classification requirements (i.e., cleanroom construction, retrofitting, HVAC, HEPA filters, temperature/humidity gauges) for each space. Our engineering team conducts preliminary research to determine what types of facility changes you will need to upgrade from USP 795 or USP 797 compliance.
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PAC (that’s us) helps industrial, government, and enterprise customers target a specific cleanroom classification or isolate an operation to keep it cleaner.
