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ResourcesHuman Research EthicsWho Owns Patient Data in Clinical Research? – CollabPx (Charlotte J. Haug | October 2017)

Australasian Human Research Ethics Consultancy Services Pty Ltd (AHRECS)

Who Owns Patient Data in Clinical Research? – CollabPx (Charlotte J. Haug | October 2017)

 


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Q: Many people are coming to believe that active patient participation will be a key to more rapid movement forward in cancer research. Data sharing can help. But who owns the data? And what rights and responsibilities are thus conferred? Your recent NEJM article provides helpful background. Can you help us better understand?

A: Exchange of data between patients and doctors is essential for the practice of medicine – and patient data are essential for medical research and progress.

Traditionally, doctors collected patients’ health information (typically the medical history, laboratory tests, drugs prescribed, outcome of treatment, etc.) and sometimes shared that information, in confidence, with colleagues to seek advice and advance science. The medical record was the physician’s property, and still is in many countries and legislations. But do physicians own the patient data?

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