- How Democracy Can Inform Consent: Cases of the Internet and Bioethics.Carol C. Gould - 2019 - Journal of Applied Philosophy 36 (2):173-191.details
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The Ethics of Research with Human Subjects: Protecting People, Advancing Science, Promoting Trust.David B. Resnik - 2018 - Cham: Springer Verlag.details
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Broad Consent for Research With Biological Samples: Workshop Conclusions.Christine Grady, Lisa Eckstein, Ben Berkman, Dan Brock, Robert Cook-Deegan, Stephanie M. Fullerton, Hank Greely, Mats G. Hansson, Sara Hull, Scott Kim, Bernie Lo, Rebecca Pentz, Laura Rodriguez, Carol Weil, Benjamin S. Wilfond & David Wendler - 2015 - American Journal of Bioethics 15 (9):34-42.details
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Own Data? Ethical Reflections on Data Ownership.Patrik Hummel, Matthias Braun & Peter Dabrock - 2020 - Philosophy and Technology 34 (3):545-572.details
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The biobank consent debate: why ‘meta-consent’ is still the solution!Thomas Ploug & Soren Holm - 2019 - Journal of Medical Ethics 45 (5):295-297.details
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The biobank consent debate: Why ‘meta-consent’ is not the solution?Neil C. Manson - 2019 - Journal of Medical Ethics 45 (5):291-294.details
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Coding and Consent: Moral Challenges of the Database Project in Iceland.VilhjÁlmur Rnason - 2004 - Bioethics 18 (1):27-49.details
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Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.Isabelle Budin-Ljøsne, Harriet J. A. Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D’Abramo, Heike Felzmann, Teresa Finlay, Muhammad Kassim Javaid, Erica Jones, Višnja Katić, Amy Simpson & Deborah Mascalzoni - 2017 - BMC Medical Ethics 18 (1):4.details
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The ‘Expiry Problem’ of broad consent for biobank research - And why a meta consent model solves it.Thomas Ploug & Søren Holm - 2020 - Journal of Medical Ethics 46 (9):629-631.details
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Informed consent and routinisation.Thomas Ploug & Soren Holm - 2013 - Journal of Medical Ethics 39 (4):214-218.details
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In Defence of informed consent for health record research - why arguments from ‘easy rescue’, ‘no harm’ and ‘consent bias’ fail.Thomas Ploug - 2020 - BMC Medical Ethics 21 (1):1-13.details
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“It’s my blood”: ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants.Keymanthri Moodley, Nomathemba Sibanda, Kelsey February & Theresa Rossouw - 2014 - BMC Medical Ethics 15 (1):4.details
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Broad consent for biobanks is best – provided it is also deep.Rasmus Bjerregaard Mikkelsen, Mickey Gjerris, Gunhild Waldemar & Peter Sandøe - 2019 - BMC Medical Ethics 20 (1):1-12.details
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The ethics of biobanking: Assessing the right to control problem for broad consent.Neil C. Manson - 2019 - Bioethics 33 (5):540-549.details
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Communicating Identifiability Risks to Biobank Donors.T. J. Kasperbauer, Mickey Gjerris, Gunhild Waldemar & Peter Sandøe - 2018 - Cambridge Quarterly of Healthcare Ethics 27 (1):123-136.details
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The Nuremberg Code.A. S. Duncan, G. R. Dunstan & R. B. Welbourn - 1981 - Journal of Law, Medicine and Ethics 19 (3-4):130--2.details
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Scientific research is a moral duty.J. Harris - 2005 - Journal of Medical Ethics 31 (4):242-248.details
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Broadening consent--and diluting ethics?B. Hofmann - 2009 - Journal of Medical Ethics 35 (2):125-129.details
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Broad consent under the GDPR: an optimistic perspective on a bright future.Dara Hallinan - 2020 - Life Sciences, Society and Policy 16 (1):1-18.details
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Controversies between regulations of research ethics and protection of personal data: informed consent at a cross-road.Eugenijus Gefenas, J. Lekstutiene, V. Lukaseviciene, M. Hartlev, M. Mourby & K. Ó Cathaoir - 2021 - Medicine, Health Care and Philosophy 25 (1):23-30.details
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Rethinking informed consent in bioethics.Neil C. Manson - 2007 - New York: Cambridge University Press. Edited by Onora O'Neill.details
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The Re-emergence of the Liberal-Communitarian Debate in Bioethics: Exercising Self-Determination and Participation in Biomedical Research.E. Christensen - 2012 - Journal of Medicine and Philosophy 37 (3):255-276.details
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Where Did Informed Consent for Research Come From?Alexander Morgan Capron - 2018 - Journal of Law, Medicine and Ethics 46 (1):12-29.details
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From “Informed” to “Engaged” Consent: Risks and Obligations in Consent for Participation in a Health Data Repository.Elizabeth Bromley, Alexandra Mendoza-Graf, Sandra Berry, Camille Nebeker & Dmitry Khodyakov - 2020 - Journal of Law, Medicine and Ethics 48 (1):172-182.details
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Coding and Consent: Moral Challenges of the Database Project in Iceland.Vilhjálmur Árnason - 2004 - Bioethics 18 (1):27-49.details
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