Cleanroom & Aseptic Suite Validation

End-to-end cleanroom validation and environmental verification services supporting compliance, operational control, and lifecycle performance assurance.
Aligned with:
ISO
14644
EU GMP
Annex 1
MHRA
HSE
HTM 03-01

What We Test

Technical testing and environmental verification services supporting cleanroom compliance, performance and operational integrity across the full facility lifecycle.

Pressure Differentials

Room pressure and cascade balancing

Pressure Differentials

Airflow & ACR

Velocity, volume and air change rate verification

Airflow & ACR

Particle Counting

ISO classification and GMP grading

Particle Counting

Temperature & Humidity

Environmental monitoring and mapping

Temperature & Humidity

HEPA Integrity

Filter integrity testing for AHUs and terminal filters

HEPA Integrity

Recovery Testing

Recovery time and rate verification

Recovery Testing

Our Scope of Testing Include

Commissioning - IQ, OQ, PQ
Routine validation and requalification
Airflow velocity and volume testing
Air change rate verification
Pressure differential testing
HEPA filter integrity testing
Particle counting - ISO & GMP grading
Temperature and humidity mapping
Recovery time and recovery rate testing
Airflow visualisation - smoke studies
Magnehelic Gauge Verification
Microbiological monitoring - Active, Settle, Contact
Why It Matters

Why It Matters

Regular validation ensures your cleanroom operates within required limits, maintaining product quality, regulatory compliance and patient safety.

How We Work

1

Assess

We identify structural and performance issues that may impact compliance and system operation.

2

Advise

We provide recommendations based on our findings, highlighting areas for improvement.

3

Optimise

We address identified issues and implement improvements to enhance performance and compliance.

4

Test

Our engineers carry out testing in line with agreed specifications using calibrated equipment.

5

Report

You receive comprehensive, compliant reports with clear results and findings.

6

Support

Ongoing support, requalification and optimisation to maintain performance over time.

Standards & Compliance

Aligned With Industry Standards

All validation activities are carried out in accordance with ISO 14644 and EU GMP Annex 1, ensuring your facility meets regulatory expectations.

Testing in 'as built', 'at rest' and 'operational' states
GMP-compliant documentation
UKAS traceable equipment calibration
Experienced validation engineers
Industry Standards

Key Benefits

Ensure Compliance

Meet ISO, GMP and regulatory requirements

Protect Product Quality

Reduce contamination risks

Reduce Risk

Identify issues before they impact operations

Improve Performance

Maintain optimal environmental control

Technical Expertise

Delivered by experienced, fully trained engineers

Full Documentation

Clear, audit-ready reports

Speak to a Technical Specialist

Get expert support for your cleanroom, laboratory or critical environment. Our team is ready to help you achieve, maintain and demonstrate full compliance.

Request Consultation

Our Commitment to Excellence

Trusted Experience. Proven Commitment.

20+ Years of Expertise

Decades of hands-on experience in biological safety cabinet certification across a wide range of industries.

Precision Focused

We maintain the highest level of service – no shortcuts, no middle ground.

100% Commitment

Every project receives our full dedication and meticulous attention to detail.

Client Satisfaction First

Your confidence in our service is our top priority, every time.

Pride in Our Work

We take pride in delivering reliable, accurate results and stand behind every certification.

Clear & Transparent Communication

Honest, straightforward communication every step of the way so you're always informed.

AerisFlow — delivering accurate, reliable performance.

YOUR SAFETY. YOUR COMPLIANCE. PROVEN.