Access the full text.
Sign up today, get DeepDyve free for 14 days.
E. Emanuel, David Wendler, C. Grady (2000)
What makes clinical research ethical?Australasian Journal of Dermatology, 42
A. Theologis, Ronald Davis (2004)
To Give or Not to Give? That Is the QuestionPlant Physiology, 135
Margaret Chan, M. Kazatchkine, J. Lob-levyt, T. Obaid, Julian Schweizer, M. Sidibé, A. Veneman, Tadataka Yamada (2010)
Meeting the Demand for Results and Accountability: A Call for Action on Health Data from Eight Global Health AgenciesPLoS Medicine, 7
J. Baust (2008)
ISBER: Best Practices for Repositories and Trends at the Institute for Problems of Cryobiology and MedicineCell Preservation Technology, 6
R. Kirby (1982)
Ethics and Regulation Of Clinical ResearchAnesthesia & Analgesia, 61
Alison Thompson, Karen Faith, Jennifer Gibson, Ross Upshur (2006)
Pandemic influenza preparedness: an ethical framework to guide decision-makingBMC Medical Ethics, 7
Nuremberg Tribunal (1996)
The Nuremberg Code.JAMA, 276 20
S. Jasanoff (1996)
Science at the bar : law, science, and technology in AmericaContemporary Sociology, 25
S. Fienberg, Margaret Martin, M. Straf (1985)
Sharing research dataEthics & Behavior, 22
Andrew Weber, N. Lurie, S. Dowell, J. Fischer, J. Kates, S. Morrison (2010)
International Health Regulations
F. Grinnell (1987)
The Scientific Attitude
Heather Piwowar, M. Becich, H. Bilofsky, R. Crowley (2008)
Towards a Data Sharing Culture: Recommendations for Leadership from Academic Health CentersPLoS Medicine, 5
D. Guston (2007)
Between Politics and Science
B. Gray, R. Cooke, A. Tannenbaum (1978)
Research involving human subjects.Science, 201 4361
B. Gandevia, A. Tovell (1964)
DECLARATION OF HELSINKI.The Medical journal of Australia, 2
J. Kaye, C. Heeney, Naomi Hawkins, J. Vries, P. Boddington (2009)
Data sharing in genomics — re-shaping scientific practiceNature Reviews Genetics, 10
Z. Bankowski (1991)
Council for International Organizations of Medical Sciences
E. Campbell, B. Clarridge, M. Gokhale, L. Birenbaum, S. Hilgartner, N. Holtzman, D. Blumenthal (2002)
Data withholding in academic genetics: evidence from a national survey.JAMA, 287 4
C. Foster (1994)
International ethical guidelines for biomedical research involving human subjectsJournal of Medical Ethics, 20
E. Birney, T. Hudson, E. Green, C. Gunter, S. Eddy, J. Rogers, J. Harris, S. Ehrlich, R. Apweiler, Chris Austin, Lisa Berglund, M. Bobrow, C. Bountra, A. Brookes, A. Cambon-Thomsen, N. Carter, R. Chisholm, J. Contreras, R. Cooke, W. Crosby, Ken Dewar, R. Durbin, S. Dyke, J. Ecker, K. Emam, L. Feuk, S. Gabriel, J. Gallacher, W. Gelbart, Antoni Granell, F. Guarner, T. Hubbard, S. Jackson, Jennifer Jennings, Y. Joly, S. Jones, J. Kaye, Karen Kennedy, B. Knoppers, N. Kyrpides, W. Lowrance, Jingchu Luo, John Mackay, Luis Martín-Rivera, W. McCombie, J. McPherson, L. Miller, Webb Miller, Don Moerman, V. Mooser, Cynthia Morton, J. Ostell, B. Ouellette, J. Parkhill, P. Raina, C. Rawlings, S. Scherer, S. Scherer, P. Schofield, C. Sensen, V. Stodden, M. Sussman, Toshihiro Tanaka, Janet Thornton, T. Tsunoda, D. Valle, E. Vuorio, N. Walker, S. Wallace, G. Weinstock, W. Whitman, K. Worley, C. Wu, Jiayan Wu, Jun Yu (2009)
Prepublication data sharingNature, 461
Making research data readily accessible during a public health emergency can have profound effects on our response capabilities. The moral milieu of this data sharing has not yet been adequately explored. This article explores the foundation and nature of a duty, if any, that researchers have to share data, specifically in the context of public health emergencies. There are three notable reasons that stand in opposition to a duty to share ones data, relating to: (i) data property and ownership, (ii) just distribution of benefits and burdens and (iii) the contemporary ethos of science. We argue each reason can be successfully met with corresponding rationale in favour of data sharing. Further support for data sharing has been echoed in policies of health agencies, funding bodies and academic institutions; in documents on the ethical conduct of biomedical research; and in discussions on the nature of public health. From this, we ascertain that sharing data is the morally sound default position. This article then highlights the key roles reciprocity and solidarity play in supporting the practice of data sharing. We conclude with recommendations to regard public health research data as a common-pool resource in order to build a framework for stable data sharing management.
Public Health Ethics – Oxford University Press
Published: Apr 17, 2011
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.