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As a research funder and research partner of the NHS, public health and social care, the NIHR complements the work of the Medical Research Council. [5] NIHR focuses on translational research (translating discoveries from the laboratory to the clinic), clinical research and applied health and social care research. [5] [6]
There was a similar scheme in the NHS in Northern Ireland, but there has been no award scheme run for several years. [2] In the Welsh NHS there are local commitment awards for consultants and a parallel national clinical impact award scheme. Wales has an additional National 0 award level to that in England, valued at £10,000 a year also for 5 ...
This group consists of medical professionals, representatives of patient and carer groups and technical experts. They work together to assess the evidence for the guideline topic (e.g. clinical trials of competing products) before preparing a draft guideline. There are then two consultation periods in which stakeholder organisations are able to ...
Health Research Authority logo. The Health Research Authority (HRA) is an arm's length body of the Department of Health and Social Care (DHSC) in England. [1] The HRA exists to provide a unified national system for the governance of health research. The current chair of the HRA is Professor Sir Terence Stephenson, who succeeded Sir Jonathan ...
In addition to official NHS charities, many other charities raise funds that are spent through the NHS, particularly in connection with medical research and capital appeals. [citation needed] Regional lotteries were also common for fundraising, and in 1988, a National Health Service Lottery was approved by the government before being found illegal.
The Clinical Practice Research Datalink (CPRD) is an observational and interventional research service that operates as part of the Department of Health and Social Care.It is jointly funded by the National Institute for Health and Care Research (NIHR) and the Medicines and Healthcare products Regulatory Agency (MHRA).
The Cass Review, which was an independent review of gender identity services for children and young people in the NHS, said that for the majority of young people a medical pathway “may not be ...
The DRKS is an open access, free of charge online register for clinical trials and is available both in English and German. DRKS is part of the WHO's ICTRP. The DRKS works with two partner registries in Germany, DeReG (German Registry for Somatic Gene-Transfer Trials) and Clinical Trial Registry of the University Medical Center Freiburg. [4]