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Citations of this work
Biobanks--When is Re-consent Necessary?K. S. Steinsbekk & B. Solberg - 2011 - Public Health Ethics 4 (3):236-250.
A Preliminary Study to Explore the Informed Consent Approach and the Ethical Challenges in the Malaysian Biobanking for Research.Amnah Azahar, Aimi Nadia Mohd Yusof & Zahir Izuan Azhar - 2022 - Asian Bioethics Review 15 (2):141-154.
A Trade Secret Model for Genomic Biobanking.John M. Conley, Robert Mitchell, R. Jean Cadigan, Arlene M. Davis, Allison W. Dobson & Ryan Q. Gladden - 2012 - Journal of Law, Medicine and Ethics 40 (3):612-629.
Incorporating Exclusion Clauses into Informed Consent for Biobanking.Zubin Master & David B. Resnik - 2013 - Cambridge Quarterly of Healthcare Ethics 22 (2):203-212.
Breite Einwilligung (broad consent) zur Biobank-Forschung – die ethische Debatte.Gesine Richter & Alena Buyx - 2016 - Ethik in der Medizin 28 (4):311-325.
References found in this work
Declaration of Helsinki. Ethical Principles for Medical Research Involving Human Subjects.World Medical Association - 2009 - Jahrbuch für Wissenschaft Und Ethik 14 (1):233-238.
How Can One Person Represent Another?A. Griffiths & Richard Wollheim - 1960 - Aristotelian Society Supplementary Volume 34:187-224.
DNA databanks and consent: A suggested policy option involving an authorization model. [REVIEW]Timothy Caulfield, Ross Upshur & Abdallah Daar - 2003 - BMC Medical Ethics 4 (1):1-4.
Public attitudes to participating in UK BioBank: A DNA bank, lifestyle and morbidity database on 500,000 members of the UK public aged 45–69. [REVIEW]Darren Shickle, Rhydian Hapgood, Jane Carlisle, Phil Shackley, Ann Morgan & Chris McCabe - 2003 - In Bartha Maria Knoppers (ed.), Populations and genetics: legal and socio-ethical perspectives. Boston: Martinus Nijhoff.
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