Page results
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Jo Moss has been appointed as director of strategy. Jo is currently chief strategy and transformation officer for North East London Integrated Care Board. Before this she was director of…
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Dozens of babies with spina bifida have been spared paralysis and other life-limiting conditions after a cutting-edge procedure first carried out in the UK by a team of clinicians from UCLH, University Hospitals Leuven in Belgium and Great Ormond Street Hospital for Children NHS Foundation Trust (GOSH) was made available on the NHS.
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Our research The role of research in the adolescent rheumatology clinic is to make sure the care we deliver to patients is the best possible, by using evidence-based practice. Research is fully…
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A mother has written a book about her experience of having a premature baby cared for in the neonatal unit at UCLH.
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Staff at University College London Hospitals recently had the privilege of meeting Barbara Fountain, founder of the global peer-to-peer support group, Young Tongues. Barbara gave a presentation on her…
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Our academic partner UCL has been placed seventh globally for medicine and first for education in the QS World University Rankings by Subject 2022.
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UCL has been ranked number one in the UK in medicine, health and the life sciences for the quality of its research.
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Address Haemostasis Research Unit University College London 1st floor, 51 Chenies Mews London, WC1E 6HX Telephone: 020 7679 6422 Email: louisa.keogh@nhs.net or …
File results
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FOI/2023/0064 - Children's operations cancelled/ delayed for non-clinical reasons from 2018 to 2022
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FOI/2023/0065 - A&E deaths from 2010 to 2022
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FOI/2023/0072 - Contact centre
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FOI/2023/0073 - Telephony and UC/ collaboration, Microsoft 365 licence and on-premise or cloud storage
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FOI/2023/0078 - Total loss written off in 2021/22
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FOI/2023/0088 - Appointments changed from in person to telephone due to industrial action
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FOI/2021/0284 - Sleep respiratory service
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FOI/2023/0099 - Number of autoclaves used at Trust
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FOI/2023/0101 - Trauma protocols in pregnant patients
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FOI/2023/0103 - Genetic Haemochromatosis patients