Page results
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There are rail strikes currently planned for Wednesday 27, Saturday 31 of July.
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The NHS has become the first healthcare system in the world to provide a new blood group genotyping test which is set to transform care for patients living with sickle cell disorder and thalassaemia.
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Our staff have rated UCLH as the top trust in London to work at, and the third best in the country, during what has been another incredibly challenging year.
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The Clinical Research Facility at UCLH has been awarded £10 million in funding to deliver cutting edge early phase health research in areas including cancer and dementia.
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This page explains what patient-initiated follow-up (PIFU) involves after your treatment for endometrial (uterine or womb) cancer.
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North Mid, UCLH and Whittington Health are running a fun, uplifting, informative event for people with sickle cell on Saturday 25th June 2022.
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UCLH Pain Management Centre is a nationally recognized centre of excellence for people with longstanding pain.
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While you're pregnant you will have a nominated professional lead which will be a midwife or an obstetrician.
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UCLH has recruited the first patient in Europe for an early phase trial of a potential new medicine for patients that have a specific sub-type of multiple myeloma (MM), a type of bone marrow cancer.
File results
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FOI/2023/0237 - Software solution to manage patient e-consent for school vaccinations/ immunisations and waitlist validation
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FOI/2023/0244 - IT systems for digital dictation, speech recognition, outsourced transcription, video consultation and health information systems
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FOI/2023/0247 - Treatment guidelines for Idiopathic Pulmonary Fibrosis
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FOI/2023/0242 - Treatment of Haemophilia A
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FOI/2023/0262 - Clinical trial participation
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FOI/2023/0360 - Minutes of Board of Director meetings and Declarations of Interests (DoI) statements 2008-2023
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FOI/2023/0275 - Trust statistics on spiking
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FOI/2023/0231 - Patients seen at A&E with symptoms of taking nitrous oxide gas
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FOI/2023/0332 - Eating disorder services and Advance Decisions/ Directives to refuse medical treatment (ADRTs)
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FOI/2023/0260 - Treatment for rare diseases: Fabry, Gaucher and Pompe disease and Hunter Syndrome