A newly commissioned cleanroom, or one that has just been modified — a changed layout, a relocated piece of equipment, a filter bank replacement — hasn't yet demonstrated that it performs to the classification it was designed for. Clean room qualification is the baseline testing exercise that closes that gap: it measures the space against its intended design classification before, or immediately after, it is put into operational use.
This is different from a routine test on an already-running room, and different from a scheduled validation programme that re-confirms performance over time. Qualification is tied to an event — a new facility, a modification, a relocation — not a calendar.
Operation theatres & critical care
Manufacturing & sterile areas
Research & QC environments
Precision manufacturing
We review the room's intended classification, layout and design documentation before testing begins.
Testing is carried out against ISO IEC 17025:2017 procedures to confirm the space performs to its design intent.
You receive a report confirming baseline performance, ready for your commissioning or handover file.
Where a future modification could affect performance, we advise on when the space should be requalified.