Literature DB >> 15072055

Learning from experience: privacy and the secondary use of data in health research.

William W Lowrance1.   

Abstract

In this fast-moving age of data banking, data are a currency, and often a commodity. Electronic health records are being developed everywhere. Increasingly, data collected for various primary purposes are being re-used for research. With personal mobility, contracting of services, and telemedicine, health care data are crossing national borders, and therefore so are genetic information, biological materials, and reimbursement data. There is much public and legal concern about the implications. This article addresses the question: Under what conditions may data not collected specifically for research, such as primary medical data, be re-used for health research without compromising the privacy of the data-subjects?

Keywords:  Biomedical and Behavioral Research; Data Protection Act 1998 (Great Britain); Legal Approach; National Health Service

Mesh:

Year:  2003        PMID: 15072055

Source DB:  PubMed          Journal:  J Biolaw Bus        ISSN: 1095-5127


  9 in total

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6.  Criminal Prohibition of Wrongful Re‑identification: Legal Solution or Minefield for Big Data?

Authors:  Mark Phillips; Edward S Dove; Bartha M Knoppers
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7.  Informed consent and registry-based research - the case of the Danish circumcision registry.

Authors:  Thomas Ploug; Søren Holm
Journal:  BMC Med Ethics       Date:  2017-09-15       Impact factor: 2.652

8.  The anatomy of electronic patient record ethics: a framework to guide design, development, implementation, and use.

Authors:  Tim Jacquemard; Colin P Doherty; Mary B Fitzsimons
Journal:  BMC Med Ethics       Date:  2021-02-04       Impact factor: 2.652

9.  Examination and diagnosis of electronic patient records and their associated ethics: a scoping literature review.

Authors:  Tim Jacquemard; Colin P Doherty; Mary B Fitzsimons
Journal:  BMC Med Ethics       Date:  2020-08-24       Impact factor: 2.652

  9 in total

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