The Ethics and Laws of Medical Big Data (under review)

Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

The COVID-19 pandemic has highlighted that leveraging medical big data can help to better predict and control outbreaks from the outset. However, there are still challenges to overcome in the 21st century to efficiently use medical big data, promote innovation and public health activities and, at the same time, adequately protect individuals’ privacy. The metaphor that property is a “bundle of sticks”, each representing a different right, applies equally to medical big data. Understanding medical big data in this way raises a number of questions, including: Who has the right to make money off its buying and selling, or is it inalienable? When does medical big data become sufficiently stripped of identifiers that the rights of an individual concerning the data disappear? How have different regimes such as the General Data Protection Regulation in Europe and the Health Insurance Portability and Accountability Act in the US answered these questions differently? In this chapter, we will discuss three topics: (1) privacy and data sharing, (2) informed consent, and (3) ownership. We will identify and examine ethical and legal challenges and make suggestions on how to address them. In our discussion of each of the topics, we will also give examples related to the use of medical big data during the COVID-19 pandemic, though the issues we raise extend far beyond it.
Original languageEnglish
Title of host publicationThe Cambridge Handbook of Life Science, Information Technology and Human Rights
Number of pages18
PublisherCambridge University Press
Publication statusSubmitted - 31 Jul 2020

    Research areas

  • Faculty of Law - Big data, Ethics, Ownership, COVID-19, Data Sharing, informed consent, EU Law, US Law

ID: 245426353