Provision of Culture Media, Labware and Embryoslides

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        {
            "id": "GB-PPON-PXGG-1229-JLQM",
            "name": "QE Facilities Ltd",
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            "contactPoint": {
                "name": "Steven McCallum QEF/QEH",
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                "postalCode": "CV34 4HL",
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                "countryName": "United Kingdom",
                "region": "UKG13"
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            "contactPoint": {
                "email": "Kgresty@vitrolife.com"
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            "id": "2023/54",
            "scheme": "UKPGA",
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        "title": "Provision of Culture Media, Labware and Embryoslides",
        "description": "A 5 year price agreement for the provision of Culture Media, Labware and Embryoslides for use within the Gateshead Fertility Services. Cost based on previous 12 months spend is estimated to be PS323,124.75 ex VAT, PS387,749.70 inc VAT over the term of the 5 year agreement",
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        "procurementMethod": "direct",
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        "procurementMethodRationale": "Embryo culture media is a critical component of the IVF process, with a direct impact on embryo development, clinical pregnancy rates, and potentially the long-term health outcomes of resulting offspring. Any change in culture media therefore represents a significant clinical decision with inherent risk. It is not feasible to conduct a tandem trial using multiple media products concurrently within our service. Such an approach would require formal ethical approval and would introduce substantial complexity into routine clinical practice. Furthermore, any transition between media systems would necessarily affect all patients undergoing treatment during that period, thereby exposing them to potential variability in outcomes. While retrospective analysis could be undertaken to evaluate the impact of a change on key performance indicators, this would only be possible after implementation, at which point any negative effects on patient outcomes would already have occurred. In addition, EmbryoScope time-lapse incubators require the use of EmbryoScope-specific culture dishes (slides), which are the only compatible consumables for this equipment. This creates a technical dependency that further limits the ability to consider alternative suppliers. For these reasons, this direct award is justified under Section 41 of the Procurement Act 2023, relying on Schedule 5, paragraph 6 (single supplier: technical reasons). The requirement can only be supplied by a particular supplier due to technical compatibility and the absence of reasonable alternatives. A change in supplier would result in incompatibility and/or disproportionate clinical and operational risk.",
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