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    Heterogeneity in IRB Policies with Regard to Disclosures About Payment for Participation in Recruitment Materials.Megan S. Wright & Christopher T. Robertson - 2014 - Journal of Law, Medicine & Ethics 42 (3):375-382.
    Although the Federal Common Rule requires that informed consent documents include all material information, it does not specify the content of materials used to recruit human subjects. In particular, there is no federal regulation relating to how payment for research participation is to be advertised. Rather, the FDA has issued guidance, advising researchers not to emphasize payment information. In order to determine how IRBs have interpreted this guidance, we coded the policies of the top 100 institutions by receipt of NIH (...)
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  2. Heterogeneity in IRB Policies with Regard to Disclosures About Payment for Participation in Recruitment Materials.Megan S. Wright & Christopher T. Robertson - 2014 - Journal of Law, Medicine and Ethics 42 (3):375-382.
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  3. Guardianship and Clinical Research Participation: The Case of Wards with Disorders of Consciousness.Megan S. Wright, Michael R. Ulrich & Joseph J. Fins - 2017 - Kennedy Institute of Ethics Journal 27 (1):43-70.
    Incapacitated adults with a legally appointed guardian or conservator may be recruited for or involved with medical, behavioral, or social science research. Much of the research in which such persons participate is aimed at evaluating medical interventions for them, or contributing to general knowledge about disorders from which they may suffer. In this paper we will consider how the appointment of guardians for patients with disorders of consciousness —severe brain injuries that affect a patient’s level of arousal and ability to (...)
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