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The International Benchmarking of Childhood Cancer Survival is a research collaboration between multiple population-based cancer registries within and outside of Europe looking to understand why there are variations in childhood cancer survival rates between countries and to highlight any areas that...
NIPT is a way of screening for Down’s syndrome, Edwards' syndrome and Patau's syndrome in a developing baby. NCARDRS supports the evaluative rollout of NIPT by collating the screening data and linking it to registration data.
Patient data was used to measure the benefits of a new treatment for lung cancer
Discover how patient data is being used to improve sarcoma care in England
The International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR) is a voluntary non profit International Organisation affiliated with the World health organisation.
The Ovarian Cancer Audit Feasibility Pilot (OCAFP) is a jointly funded partnership project with the British Gynaecological Cancer Society, Ovarian Cancer Action and Target Ovarian Cancer.
The National Disease Registration Service (NDRS) supports NHS England to improve data collected on cancer recurrence, progression and transformations.
Learn about the Ovarian Cancer Audit Feasibility Pilot (OCAFP), a 3 year collaboration between the charity sector and analysts at the National Disease Registration Service.
EUROCAT is the European network of population-based registries for the epidemiological surveillance of congenital anomalies.
The cancer Quality of Life (QOL) is national survey run by NHS England, aimed at finding out how quality of life may have changed for people diagnosed with cancer.
