CLIMATE GRIP
Non-Viable Particle Count Test
SERVICE / 02Cleanroom Classification

Non-Viable Particle Count Test

Airborne particle measurement and cleanroom classification for controlled manufacturing and research environments.

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Measured
Documented
Why this test matters

Evidence for confident environmental control.

Calibrated aerosol particle counters quantify and size airborne particles to establish the actual cleanliness level of a controlled space. Sampling can be performed in the As-Built, At-Rest or Operational state so the result reflects the facility condition required by the validation plan.

A documented view of airborne particulate performance across the tested environment.
Particle Count Testing reference from the Climate Grip company brochure
Validation activity from the company brochure
Typical scope

Defined around the room, risk and required evidence.

Use particle classification during facility qualification, after significant HVAC or layout changes, and at the periodic frequency established by the contamination-control programme.

  • Cleanrooms and controlled support spaces
  • Defined particle sizes and classification limits
  • Representative sampling locations
  • Room state and operating-condition observations
Our method

A disciplined path from measurement to report.

01
Stage 1

Confirm room state, classification target and sampling grid

02
Stage 2

Establish sample locations and calibrated flow volume

03
Stage 3

Collect and review particle data at each location

04
Stage 4

Compare results and issue traceable classification records

Climate Grip Particle Count Testing field service
On-site validation by Climate Grip
Validation framework

Testing aligned with the operating context.

The final protocol is confirmed against the facility classification, process risk and applicable quality requirements.

  • As-Built testing
  • At-Rest testing
  • Operational testing
Reporting package

Results your engineering and quality teams can use.

Every assignment is structured for review, traceability and practical follow-through.

01

Sampling plan and room-state record

02

Location-by-location particle results

03

Classification comparison and exception summary

04

Signed test report with equipment traceability

Need a clear validation scope?

Plan the test with our technical team.

Discuss your requirement