Cleanroom Testing & Validation
With unrivalled expertise and decades of proven delivery, Total Clean Air builds world-class cleanrooms you can trust. We support many industries with cleanroom validation services & cleanroom testing including UKAS-aligned compliance support.
Cleanroom Validation & Testing
End-to-end, UKAS-aligned validation delivering certainty, compliance, and audit readiness.
We provide a full-service testing and validation offering, ensuring that cleanrooms, biosafety labs, extraction systems and controlled environments are not just built to specification, but proven to perform precisely, safely and in full regulatory and compliance alignment. We equip your facility with scientifically robust, independently verified validation, giving you long-term assurance, audit readiness, and peace of mind.
Our experienced, accredited engineers (CTCB and CPD-trained and working to UKAS ISO 17025 standards) deploy state-of-the-art testing protocols to put your facility through rigorous validation. From airflow mapping and filter integrity to environmental monitoring and containment testing. We ensure every aspect of your controlled environment meets or exceeds requirements.
Cleanroom Testing & Validation: On-Site Steps
Our expert-led cleanroom validation services & testing ensures your facility operates within strict environmental parameters at all times Our accredited engineers follow a systematic, hands-on approach to ensure every aspect of your cleanroom or controlled environment meets design, performance, and compliance requirements.
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Preparation & Baseline Assessment
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Airflow & Pressure Testing
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Filtration & Containment Verification
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Environmental & Operational Monitoring
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Reporting & Compliance Documentation
Comprehensive Cleanroom Validation for Regulated Environments
Our expert-led cleanroom validation services are designed to ensure your controlled environments operate at peak performance while meeting stringent regulatory expectations. Through precise cleanroom validation, we assess every critical parameter—from airflow and pressure differentials to particle counts and environmental conditions—giving you complete confidence in your facility. Our structured approach to cleanroom testing helps identify risks early, maintain ISO classifications, and support consistent product quality across pharmaceutical, biotech, and advanced manufacturing settings.
Cleanroom Validation and Testing Backed by UKAS-Aligned Compliance Support
In addition to core validation, we provide detailed cleanroom ventilation verification to confirm that your air handling systems are functioning efficiently and within required tolerances. Every project is backed by robust documentation and UKAS-aligned compliance support, ensuring you are always audit-ready and aligned with industry standards. Whether you are commissioning a new facility or maintaining an existing one, our comprehensive cleanroom validation services deliver accuracy, reliability, and peace of mind.
End-to-End Cleanroom Services for Full Compliance
Total Clean Air provides end-to-end services for cleanroom projects, from cleanroom construction to decontamination solutions. We also offer dedicated maintenance and servicing solutions to keep cleanroom and ventilation systems operating at peak performance. This includes routine inspections, filter replacements, airflow and pressure checks, and preventative servicing to identify issues before they impact compliance or performance. By combining proactive maintenance with responsive support, their service helps extend equipment lifespan, minimise downtime, and ensure cleanrooms consistently meet required standards without disruption.
We offer a comprehensive suite of testing and cleanroom validation services to suit a wide range of cleanroom types, clean-air systems, and controlled-environment applications — from pharmaceutical cleanrooms to biosafety labs, HVAC and LEV systems, and beyond.
Cleanrooms, Laminar Flow
& Controlled Environments
Full qualification and validation of cleanrooms and laminar-flow systems, including airflow mapping, HEPA/ULPA filter integrity, pressure-cascade verification, particle counts (at rest and in operation), and environmental stability (airflow uniformity, velocity, temperature, and humidity).
Biosafety, Containment
& Specialist Facilities
Comprehensive validation of biosafety labs (CL2/CL3), containment suites, and high-risk or sensitive environments. Services include air-handling and pressure systems testing, airflow visualisation (smoke testing), barrier and filter integrity, interlock verification, containment performance, and operator/product protection assurance.
HVAC, Extract Ventilation
& Exhaust Systems
Testing and certification of HVAC installations, LEV systems, fume cupboards (ducted and ductless), and extract/exhaust systems. This includes airflow volume and velocity surveys, room pressure balancing, hood and capture performance, duct leakage, filter performance, IAQ, thermal comfort, and compliance with relevant standards.
Validation Management, Documentation
& Re-Qualification
End-to-end validation support including Validation Master Plans (VMP), IQ/OQ/PQ protocol development, and detailed audit-ready reporting. We also provide deviation management, corrective actions, trend analysis, ongoing monitoring, and scheduled re-validation to maintain long-term compliance.
Cleanrooms, Laminar Flow
& Controlled Environments
Full qualification and validation of cleanrooms and laminar-flow systems, including airflow mapping, HEPA/ULPA filter integrity, pressure-cascade verification, particle counts (at rest and in operation), and environmental stability (airflow uniformity, velocity, temperature, and humidity).
Biosafety, Containment
& Specialist Facilities
Comprehensive validation of biosafety labs (CL2/CL3), containment suites, and high-risk or sensitive environments. Services include air-handling and pressure systems testing, airflow visualisation (smoke testing), barrier and filter integrity, interlock verification, containment performance, and operator/product protection assurance.
HVAC, Extract Ventilation
& Exhaust Systems
Testing and certification of HVAC installations, LEV systems, fume cupboards (ducted and ductless), and extract/exhaust systems. This includes airflow volume and velocity surveys, room pressure balancing, hood and capture performance, duct leakage, filter performance, IAQ, thermal comfort, and compliance with relevant standards.
Validation Management, Documentation
& Re-Qualification
End-to-end validation support including Validation Master Plans (VMP), IQ/OQ/PQ protocol development, and detailed audit-ready reporting. We also provide deviation management, corrective actions, trend analysis, ongoing monitoring, and scheduled re-validation to maintain long-term compliance.
Total Clean Air offers a complete turnkey package for all your cleanroom requirements
Testing & Validation
Why Choose Total Clean Air for Your Testing & Validation Needs
As a UKAS ISO 17025-accredited organisation, we provide our clients with independent, scientifically validated results. These represent not merely a certificate, but robust, defensible documentation recognised and trusted by regulators worldwide.
We combine deep technical expertise with extensive multi-sector experience, spanning pharmaceuticals, biotechnology, healthcare, aerospace, and advanced manufacturing. This breadth of knowledge ensures we fully understand your regulatory, contamination control, and operational requirements.
Our comprehensive range of services, from design and build through testing, validation, and long-term lifecycle support enables you to work with a single, trusted partner. Whether commissioning a new facility, re-qualifying an existing cleanroom, or maintaining compliance over time, Total Clean Air is committed to supporting you at every stage.
At Total Clean Air, we care about the long-term success of your facility. We provide more than compliance; we deliver peace of mind. You can be confident that your environment not only meets design specifications but demonstrably performs to the required standards, ensuring safety, reliability, and regulatory compliance day after day.