Healthcare ventilation service

Ventilation Validation and Verification Testing

IOM tests critical ventilation systems to confirm performance, identify problems early and help protect patient care and service continuity.

Service overview

Is your ventilation still performing as intended?

Critical ventilation systems can lose performance over time. Changes to clinical use, maintenance issues or system faults may also affect whether an area continues to operate as intended.

IOM provides validation and verification testing to help you confirm performance, identify problems and take action before they affect patient care or service delivery.

When this service may be needed

  • A new or refurbished system requires validation
  • Annual or periodic verification is due
  • Performance concerns or changes require targeted investigation

Practical support

Confirm your systems are performing effectively

We test new, refurbished and existing ventilation systems in areas including:

  • Conventional and ultra-clean operating theatres
  • Treatment and minor procedure rooms
  • Isolation rooms
  • Recovery areas and wards
  • Sterile services departments
  • Aseptic suites and pharmacies
  • Intensive and high-dependency units
  • Mortuaries
  • Laboratories
  • In vitro fertilisation treatment suites

Our testing can include airflow measurements, pressure relationships, particle counting and air-handling unit inspections.

From evidence to action

Clear findings and practical next steps

We explain whether the system is performing against the relevant requirements and design intent. Where we identify deficiencies, we provide clear findings to help you assess the risk and prioritise corrective work.

We understand the operational pressures within healthcare. Our team plans testing around theatre and clinical schedules wherever possible.

Need to validate a new system or verify the performance of an existing one? Talk to our healthcare ventilation team.

What the service includes

Measure airflow, pressure, particles and relevant system parameters.
Test theatres, isolation rooms, aseptic areas and other specialised environments.
Assess performance against the relevant requirements and design intent.
Explain deficiencies and support corrective-action decisions.

What you receive

Clear evidence and usable next steps

  • Independent technical findings
  • Clear explanation of the risks or performance issues
  • Prioritised practical recommendations
  • Evidence to support governance, planning and assurance

Get practical advice for your organisation.

Discuss your requirements

Tell us what you need to achieve and your enquiry will be directed to the most appropriate team.

Speak to an expert