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Tag Archives: Administrative Datasets
Big Data and Public Health (Parliamentary Office of Science and Technology POST Note PN 474 / PN 468)
Summary This Parliamentary Office of Science & Technology (POST) note on “Big Data and Public Health” considers the growing use of patients’ health records and large-scale medical and administrative datasets as valuable sources of information for the study and improvement … Continue reading →
Posted in Commissioning, Department of Health, For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), National, NHS, NHS England, Public Health England, Quick Insights, Standards, Statistics, UK, Universal Interest
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Tagged Academic Research, Administrative Data, Administrative Data Research Network, Administrative Datasets, Aggregate Level Data Sources, Aggregated Data, Analytics, Anonymised Patient Medical Records, Applications of Big Data, Arts and Humanities Research Council, Avon Longitudinal Study of Parents & Children (ALSPAC), Be Clear on Cancer (BCOC), Big Data, Big Data Analytics, Big Data Funding and Research, Big Data Overview, Big Data: One of UK Government's Eight Great Technologies, Biotechnology and Biological Sciences Research Council, Care Act 2014, care.data, Care.data: Modern Data Service for the NHS, Clinical Audits, Clinical Commissioning Groups (CCGs), Clinical Practice Research Datalink (CPRD), Common Law Duty of Confidentiality, Data Extraction and Linkage, Data Linkage and Extract Service, Data Linkage to Support Surveillance, Data Protection Act (1998), Data Quality and Accuracy, Data Security and Identifiability, Data Security Techniques, Digital Care Records, Economic and Social Research Council, Eight Great Technologies, Electronic Care Records, Epidemiology, Epidemiology and Statistics, EU Data Protection Regulation, European Data Protection Regulation, Farr Institute, General Practice Extraction Service (GPES), Governance of Data Access, GPES Independent Advisory Group (IAG), Health and Social Care Act (2012), Health and Social Care Information Centre (HSCIC), Health Improvement, Health Informatics, Health Protection (Notification) Regulations 2010, Health Protection Agency, Health Service (Control of Patient Information) Regulations 2002, Healthcare Planning, Hospital Episode Statistics (HES), House of Commons Library, House of Commons Library POST Note PN 474, Human Rights Act (HRA), Increasing Efficiency, Informatics, Information Sharing, Innovation in Bioinformatics, Interoperability, Interoperability Standards, Legislation and Governance, Leveraging Big Data, Management of Big Data, Medical Informatics, Medical Research, National Cancer Data Repository, National Cancer Intelligence Network (NCIN), National Pupil Database, Natural Environment Research Council, NHS Electronic Patient Records, NHS Records, Office of National Statistics (ONS), Office of National Statistics Mortality Data, Office of Science & Technology POSTnote, Open Data, Open Data and Big Data, Open Data in Health and Social Care, Open Data in the NHS, Parliament, Parliamentary Office of Science & Technology, Parliamentary Office of Science & Technology (POST), Patient Records, Population Risk Stratification, POST Note PN 468, POST Note PN 474, POSTnote No.468, POSTnote No.474, POSTnotes, Primary Use Within the NHS, Pseudonymised Data, Public Health, Public Health and Health Improvement, Public Health England (PHE), Public Health Improvement, Public Health Informatics, Public Health Monitoring, Publicly-Funded UK Big Data Research, Records Management: NHS Code of Practice, Records Standards in Health and Social Care, Risk Stratification, Risk Stratification Programmes, Routes to Diagnosis (NCIN), Science and Technology Facilities Council, Secondary Use Beyond the NHS, Secondary Use Within the NHS, Secondary Uses Data Set, Secondary Uses Service (SUS), Social Epidemiology, Standardised Electronic Health Records, Summary Care Records, Summary Level Statistics, Transparency, Transparency and Accountability, Transparency and Open Data, Transparency and Public Trust, Use of Identifiable Records Without Consent: Section 251 of the National Health Service Act 2006, Uses of Data, Uses of Medical Records
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