Behsa can conduct cleanroom validation on a quarterly, bi-annual or annual basis to ensure client compliance with relevant standards. Cleanroom validation gives a complete overview of how well the cleanroom is operating. Behsa can conduct feasibility studies which outline any changes required to an existing cleanroom ensure regulatory compliance is met. Prior to a new cleanroom being installed, design data can be reviewed to ensure the system can be easily validated on an ongoing basis. Ensures Cleanroom is designed to be accessible to testing in line with ISO 14644 and WHO guidelines.
Laboratory Equipment Validation:
behsa carry out annual or bi-annual validation of Laminar Airflow Devices, Microbiological Safety Cabinets, Fan filter unit, Dispensing and Sampling Booth and Isolators.
Tests carried out on these devices include:
- Filter integrity testing (DOP testing)
- Sampling for airborne particles
- Airflow – Differential Pressures
- Airflow – Volumes and Air
- Change rates
- Airflow – Uniformity analysis
- Airflow – Visualisation
- Temperature & Humidity Test
Our range of clean air equipment servicing includes:
- HEPA filter inspection and replacement
- Isolators
- Powder Control Booths
- Extract air cabinets
- Safety cabinets
- Microbiological Safety
- abinets
- Vertical Laminar Flow Modules
- Operating Theatre filtered flow systems
- Carbon Filter saturation cabinet tests
- Clean rooms
- Down flow and Containment Booths
- Air Handling Unit filters
- Fume Cupboards Clean Air Workstations
- S.H.H./L.E.V. checks
- Dust Extractor UnitsB
