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MEDICAL GAS SAFETY PSV PSV


Primary control panel


G


Primary LOX Tank


PSV evaporators Assembly Line Valve Valve Line NC


Return valave


Non


Line Valve Line


Inside the curtilage of the building Line


Assembly Valve Main PSV Regulator G PSV Regulator Lag PSV P Lead


G


PSV


P Assembly Valve Line


Assembly


Valve


Pipeline System


Main LOX Supply on external plinth


Secondary Automatic Manifold Supply


To


xxxxxxxx


Primary, secondary, and tertiary: resilience beyond standby plant Part A also strengthens how resilience is addressed through primary, secondary, and tertiary supplies. This terminology moves the discussion beyond the assumption that resilience is achieved simply by installing duty and standby plant. The more important question is what supply remains available if the normal source, or the route from that source, is compromised. The primary supply supports normal operation. The secondary arrangement provides continuity following the relevant failure scenario. Tertiary provision adds a further layer, determined through the IDP and the clinical risk. Depending on the system and application, that could involve a further fixed pipeline source, a portable manifold, or individual cylinders. The exact arrangement is less important than the principle: the organisation should know how essential patients will continue to receive gas if the first layers of resilience are unavailable. Tertiary supply therefore connects engineering design


directly with emergency and clinical contingency planning. It needs sufficient capacity for the intended scenario, a practical method of deployment or changeover, trained staff, appropriate connections, and a clear understanding of which clinical services are prioritised. A tertiary source that exists on a drawing but cannot be deployed safely or quickly is not meaningful resilience. This is particularly relevant to oxygen. COVID-19


showed that a hospital can have adequate bulk storage while still encountering delivery constraints. Resilience must be considered along the entire chain: storage, evaporators, pressure regulation, distribution mains, risers, branches, area valves, terminal units, and the patient interface. Primary, secondary, and tertiary supplies add protection, but the distribution network must still be capable of carrying the required flow.


Validation and verification: prove the system before it is released for use One of the most important improvements in Part A is the


greater prominence given to validation and verification. This matters because an MGPS can appear complete while still containing defects concealed above ceilings, within risers, or inside a complex sequence of valves and connections. Once the system is placed into clinical service, those defects may only become visible when a patient depends on the supply. The strengthened approach clarifies the assurance sequence. Design defines what the system must achieve. Installation creates a physical system. Engineering validation and verification then confirm that the installation aligns with the design intent and performs correctly. Separate pharmaceutical quality-control testing confirms that the medicinal gas delivered through the system meets the required quality before the relevant sections are released for use. That distinction between engineering verification


and pharmaceutical quality matters. The engineer can demonstrate pressure, flow, identity, alarm operation, valve function, and other engineering requirements, but medical gases are medicines. The final assurance chain therefore needs appropriate pharmacy and QC input alongside engineering evidence. Neither discipline is replaced by the other. The more robust process also improves handover.


Test results, material information, drawings, design assumptions, and commissioning evidence should not be treated as temporary project paperwork. They form part of the technical file and the wider golden thread of information that future APs, designers, maintainers, and governance teams may need when the system is modified or investigated years later. This is ultimately a patient-safety issue. If an


organisation cannot demonstrate what was installed, what was tested, what performance was achieved, and what limitations were accepted, it inherits uncertainty. Part A’s stronger validation, verification, and information requirements are intended to reduce that uncertainty before the system becomes operational.


Figure 2: Liquid Oxygen Supply example.


Rob McCrea


Rob McCrea has worked within the Medical Gas Pipeline Systems (MGPS) industry since 1986, gaining extensive experience with several specialist companies before establishing his own business in 1994. A recognised MGPS specialist and Expert Witness, Rob acts as an Authorising Engineer (MGPS) for both NHS organisations and the Ministry of Defence and is an author of HTM 02-01:2026.


October 2026 Health Estate Journal 65


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