Cleanroom corridor with workstations

Cleanroom performance testing and ISO 14644 certification in Singapore

Independent, NEBB-certified testing to ISO 14644, FS 209E, and IEST standards. Covering cleanrooms, laminar flow cabinets, HVAC systems, controlled environments, and compressed gases.

Overview

Clean Aire is an independent, NEBB-certified cleanroom testing and certification specialist delivering ISO 14644-compliant measurement across pharmaceutical, semiconductor, healthcare, and research facilities since 2010.

Our ISO 9001:2015-governed methodology combines on-site testing to internationally recognised standards (ISO 14644, FS 209E, IEST RP), traceable instrumentation calibration, and peer-reviewed reports — evidence your regulators, auditors, and insurers accept without question.

  • NEBB Certified
    NEBB Certified National Environmental Balancing Bureau
  • ISO 9001:2015
    ISO 9001:2015 Quality Management System Certified
  • SAC Accredited
    SAC Accredited Singapore Accreditation Council certification body
  • bizSafe3
    bizSafe3 Workplace Safety & Health
Cleanroom maintenance and validation near airlock door

Services

From third-party cleanroom certification to HVAC airflow balancing, microbiological monitoring, and airflow visualisation, we deliver a full suite of controlled-environment testing to ISO 14644 and NEBB standards. Each service is calibrated to the regulatory, safety, and operational demands of Singapore's pharmaceutical, semiconductor, and healthcare facilities.

  1. 01

    Cleanroom Certification & Performance Testing

    ISO 14644-1 classification, ISO 14644-2 monitoring, and ISO 14644-3 test methods — non-viable particle counts, recovery tests, pressure cascades, and HEPA installation leak tests, delivered as peer-reviewed certification reports.

  2. 02

    Clean Air Equipment Testing

    Face velocity, HEPA integrity via PAO/DOP aerosol challenge (IEST-RP-CC034), containment testing per NSF/ANSI 49, and smoke-pattern visualisation — covering laminar flow cabinets, clean booths, biological safety cabinets, fume hoods, and isolators.

  3. 03

    HVAC Airflow Measurement & Balancing

    NEBB-certified procedures for air-change-rate calculation, pressure-differential verification, and multi-point Pitot-traverse balancing — ensuring supply, return, and exhaust conform to facility design intent and GMP operational envelopes.

  4. 04

    Microbiological & Air Quality Monitoring

    Viable sampling via settle plates and active air impaction (TSA/SDA), contact-plate swabbing, non-viable particulate counts per ISO 14644-1, and SS554 indoor air quality — CO₂, CO, formaldehyde, VOCs, and particulates for pharmaceutical, healthcare, and educational environments.

  5. 05

    Compressed Dry Air & Process Gas Testing

    Dewpoint, oil aerosol, oil vapour, particulate, and microbiological verification to ISO 8573-1 purity classes — validating the compressed air, nitrogen, and process gases feeding your critical production environments.

Technician running equipment checklist on tablet
Cleanroom operators behind protective curtains
Wide cleanroom with swirl diffusers and HVAC infrastructure
Technician sanitising gloved hands during environmental sampling
Technician monitoring compressed dry air gauges at cleanroom equipment panel
Trusted by

Our testing and certification services support pharmaceutical, semiconductor, healthcare, and research facilities across Singapore and the region.

  • Pharmaceuticals
  • Semiconductors / Electronics
  • Healthcare
  • Food & Beverages
  • Bio-Science
  • Schools & Institutions
  • Research Laboratories
  • Pfizer
  • Novartis
  • Roche
  • AbbVie
  • BioNTech
  • Mead Johnson
  • STMicroelectronics
  • UMC
  • Soitec
  • Coherent
  • National University Hospital
  • DSO National Laboratories

Need your cleanroom tested to ISO 14644 or FS 209E?

Our NEBB-certified team delivers audit-ready particle counts, recovery tests, smoke studies, and HVAC balancing — with peer-reviewed reports regulators and GMP auditors accept without question.

Schedule an Audit