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Governing the research-care divide in clinical biobanking: Dutch perspectivesEthical and deontological issues in Transfusion MedicineEvaluating the consent preferences of UK research volunteers for genetic and clinical studiesActive choice but not too active: public perspectives on biobank consent models.Consent for the use of human biological samples for biomedical research: a mixed methods study exploring the UK public's preferences.Big Data in medical research and EU data protection law: challenges to the consent or anonymise approachPublic perspectives on biospecimen procurement: what biorepositories should considerBiobanking residual tissues.Biobanking research on oncological residual material: a framework between the rights of the individual and the interest of society.Extending the surrogacy analogy: applying the advance directive model to biobanks.Ethical aspects of human biobanks: a systematic review.Can Broad Consent be Informed Consent?A Randomised Controlled Trial of Consent Procedures for the Use of Residual Tissues for Medical Research: Preferences of and Implications for Patients, Research and Clinical Practice.The Bio-PIN: a concept to improve biobanking.Informed consent for living donation: a review of key empirical studies, ethical challenges and future research.Why do participants enroll in population biobank studies? A systematic literature review.Survey of motivation to participate in a birth cohort.Participants' Understanding of Informed Consent for Biobanking: A Systematic Review."Trust is not something you can reclaim easily": patenting in the field of direct-to-consumer genetic testing.An Assessment of a Shortened Consent Form for the Storage and Research Use of Residual Newborn Screening Blood Spots.Withdrawal from biobank research: considerations and the way forward.Consent and research governance in biobanks: evidence from focus groups with medical researchers.The ethics of biobanking: key issues and controversies.The Googlization of health research: from disruptive innovation to disruptive ethics.Good health checks according to the general public; expectations and criteria: a focus group study.Q56775158
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
Reconsidering the value of consent in biobank research.
@en
Reconsidering the value of consent in biobank research.
@nl
type
label
Reconsidering the value of consent in biobank research.
@en
Reconsidering the value of consent in biobank research.
@nl
prefLabel
Reconsidering the value of consent in biobank research.
@en
Reconsidering the value of consent in biobank research.
@nl
P1433
P1476
Reconsidering the value of consent in biobank research.
@en
P2093
Beverley McNamara
Judy Allen
P304
P356
10.1111/J.1467-8519.2009.01749.X
P577
2011-03-01T00:00:00Z