Service
Clean Air Technologies will provide peace of mind that the report provided for any cleanroom, bio-containment or hospital facility which we have validated will comply with the highest current regulatory requirements.
Our dedicated team of validation engineers are internally accredited through a rigorous training process, providing documented records of competency in specialist validation techniques. All engineers are fully equipped with state-of-the-art test instruments and are trained in providing targeted diagnostics to underperforming systems.
Based strategically, throughout the UK, we can provide flexible support and
a consistent high quality of service, to a specialist client base.
Cleanroom and Clean Zones
Validation to ISO14644/cGMP requirements:
- HEPA Filter Integrity Testing
- Airborne Particle Counting
- Room Recovery Rates
- Air Change Rates
- Room Pressure Cascades
- Airflow Visualisation
- Critical Air System Re-balancing and Commissioning
Bio-containment Facilities (BSL3, BSL4)
Validation to HSE/ACDP/SAPO requirements:
- HEPA Filter Integrity Testing
- Room Pressure Cascades
- Room Sealability Testing
- Smoke Pencil Testing of Room Penetrations
- Fumigation Cycle Verification Tests
- Biological Safety Cabinet Testing
- Critical Air System Re-balancing and Commissioning
Hospital Facilities
Validation of specialist healthcare facilities to cGMP and HTM03 requirements:
- HEPA Filter Integrity Testing
- UCV Theatre Hood Validation
- General Theatre Ventilation Testing
- Pharmacy Cleanroom and Isolator Testing
- Laminar Air Flow Cabinet Testing
- Biological Safety Cabinet Testing
- Critical Air System Re-balancing and Commissioning
Our comprehensive validation reports are guaranteed within ten working days of visit and provide:
- Clear interpretation and summary of test results
- Graphical representation of the data
- 2D drawings of facility
- Detailed test methods and calibration details