VENTILATION SYSTEMS
Healthy air: Guidance to guaranteed compliance
Mathew Hopwood, Sales director at Mansfield Pollard, explores the evolving role of HTM 03-01 in healthcare ventilation. He argues for a more structured approach to compliance, acknowledges industry resistance, and calls for closer collaboration between manufacturers and industry bodies like IHEEM to ensure safer, more consistent air management across healthcare estates.
In healthcare environments, ventilation is far more than a background utility, it is a clinical safeguard. The systems that manage it are integral to infection prevention, patient safety, and the overall resilience of healthcare infrastructure. From operating theatres to isolation rooms, the quality and control of air can directly influence clinical outcomes. Yet despite this critical role, the UK healthcare sector still relies on guidance rather than enforceable standards. At Mansfield Pollard, we believe it’s time for a more robust, system-wide approach. As specialists in air management, and manufacturers
of HTM 03-01 compliant air handling units, we’ve seen first-hand the benefits of rigorous design, validation, and performance assurance. We’ve also seen the confusion, inconsistency, and missed opportunities that arise when compliance is treated as open to interpretation rather than a defined benchmark. We aren’t calling for a blanket regulation. Rather,
we’re calling for clarity, collaboration, and smarter specification, especially in high-risk clinical areas where the consequences of poor ventilation are most severe.
The clinical imperative for ventilation Ventilation in healthcare settings is a cornerstone of clinical safety. Properly designed and maintained systems ensure appropriate air change rates, pressure differentials, and filtration levels, all of which are essential to controlling airborne pathogens. In environments where patients are immunocompromised, or undergoing aerosol-generating procedures, the margin for error is slim. HTM 03-01, the Health Technical Memorandum for specialised ventilation, provides detailed guidance on achieving these outcomes. It outlines best practice for system design, installation, validation, and maintenance. However, it remains exactly that: guidance. Crucially, it is not law. Its use of advisory language, ‘should’ rather than ‘must’, creates a grey area that may compromise patient safety. The term ‘HTM-compliant’ is widely used across the
industry, but without a formal certification framework, it is often self-declared and, as a result, inconsistently applied. In fact, there is no statutory mechanism to enforce compliance. This ambiguity leads to significant variation in system performance across healthcare estates. Manufacturers, contractors, and estates teams may interpret HTM compliance differently. This inconsistency places undue pressure on authorising engineers, particularly those trained and endorsed by IHEEM, who are often engaged too late. By that point, systems are already installed and
October 2025 Health Estate Journal 141
operational, and resolving non-compliance can be costly, disruptive, or even unfeasible. We believe IHEEM’s role is essential, and should be strengthened to close this gap. Their authorising engineers are highly skilled professionals who uphold best practice and protect patient safety. However, they need greater support, particularly through earlier engagement in the design and specification process and stronger collaboration with manufacturers.
Industry resistance and misconceptions Despite the clear benefits of HTM 03-01 compliance, resistance persists across several fronts. Procurement teams may view HTM compliance as a cost burden, focusing on capital expenditure rather than lifecycle value. Yet, the long-term benefits, including reduced infection risk,
Ventilation systems are integral to infection prevention, patient safety, and the overall resilience of healthcare infrastructure.
Air handling unit designed to maintain clean, controlled air in healthcare environments.
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