Compliant. Controlled. Certified. Cleanroom Validation by Experts.
At METS Lab Abu Dhabi, we provide comprehensive Cleanroom Validation Services to ensure your controlled environments meet international cleanliness and performance standards. Whether you operate in pharmaceuticals, biotechnology, healthcare, electronics, or aerospace, cleanroom validation is a critical step in regulatory compliance and quality assurance.
We help you demonstrate that your cleanroom facilities are operating within the required ISO, EU GMP, and UAE MOHAP specifications — protecting your processes, products, and people.
Why Cleanroom Validation is Essential
Cleanrooms are designed to control airborne particulate levels, temperature, humidity, air pressure, and microbial contamination. Any deviation from required performance parameters can lead to:
- Product contamination
- Regulatory non-compliance
- Batch rejection or recall
- Risk to patient or user safety
Regular validation ensures your cleanroom consistently performs to specification, minimizing risk and ensuring confidence in your controlled operations.
Standards We Follow:
Our cleanroom validation services comply with the following international guidelines:
- ISO 14644-1 to ISO 14644-3 – Cleanroom classification & testing
- EU GMP Annex 1 – Manufacture of sterile medicinal products
- WHO GMP Guidelines
- UAE MOHAP and Health Authority – Abu Dhabi (DoH) Requirements
- Federal Standards (FED-STD-209E) –
Our Cleanroom Validation Services Include:
- Airborne Particle Count Measurement
Cleanroom classification as per ISO 14644-1 (e.g., ISO Class 5, 6, 7, 8) using calibrated particle counters.
- HEPA Filter Integrity Testing
DOP/PAO tests (smoke test) to ensure there are no leaks in filters or housing.
- Airflow Volume and Velocity Measurement
Assessment of laminar and turbulent flow regimes and proper airflow rates.
- Air Change Rate Calculation (ACH)
Evaluation of the number of air changes per hour for maintaining cleanliness levels.
- Room Pressure Differential Measurement
Verifying positive or negative pressure cascades between zones.
- Temperature & Relative Humidity Monitoring
Confirming compliance with environmental control requirements.
- Recovery Time and Containment Leak Testing
Measurement of how quickly the cleanroom returns to cleanliness post-disturbance.
- Microbiological Monitoring (Viable Count)
Air, surface, and personnel microbial monitoring using settle plates and active air samplers.
Industries We Serve:
- Pharmaceutical Manufacturing (Sterile & Non-Sterile)
- Biotechnology and Life Sciences
- Medical Device Assembly
- Hospitals and Operating Theaters
- Research Laboratories
- Semiconductor & Electronics Manufacturing
- Aerospace and Precision Engineering Facilities
