REFERENCES
- Cate, F. H., and V. Mayer-Schönberger. 2013. Notice and consent in a world of Big Data. International Data Privacy Law 3 (2):67–73. doi:10.1093/idpl/ipt005.
- Edwards, S. D. 2003. Three concepts of suffering. Medicine, Health Care, and Philosophy 6 (1):59–66. doi:10.1023/a:1022537117643.
- Fairfield, J. A., and C. Engel. 2015. Privacy as a public good. Duke Law Journal 65:385–457.
- Floridi, L. 2021. The end of an era: From self-regulation to hard law for the digital industry. Philosophy & Technology 34 (4):619–22. doi:10.1007/s13347-021-00493-0.
- Kluge, E.-H W. 2016. Ethics for health informatics professionals: The IMIA code, its meaning and implications. Geneva: International Medical Informatics Association.
- McCoy, M. S., A. L. Allen, K. Kopp, M. M. Mello, D. J. Patil, P. Ossorio, S. Joffe, and E. J. Emanuel. 2023. Ethical responsibilities for companies that process personal data. The American Journal of Bioethics 23 (11):11–23. doi:10.1080/15265161.2023.2209535.
- Sætra, H. S. 2020. Privacy as an aggregate public good. Technology in Society 63:101422. doi:10.1016/j.techsoc.2020.101422.
- Tisné, M. 2020. The data delusion: Protecting individual data isn’t enough when the harm is collective. Luminate: Building Stronger Societies.
- Van der Sloot, B., and E. Keymolen. 2022. Can we trust trust-based data governance models? Data & Policy 4:E45. doi:10.1017/dap.2022.36.
- WHO. 2021. Ethics and governance of artificial intelligence for health. Geneva: World Health Organization.