The Ancillary-Care Responsibilities of Medical Researchers: An Ethical Framework for Thinking about the Clinical Care That Researchers Owe Their Subjects

Richardson, Henry S., Belsky, Leah·2004·The Hastings Center Report
DOI 10.2307/3528248

Cited by (217)

Items 101–200 of 217

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  14. Clinical and research ethics as moral strangers
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  15. Planning for Ancillary Care Provision
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  20. Responsibilities to Plan for Ancillary Care Pose Ethical Challenges for Nutrition Research in the Community Setting ,
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  55. Selected Abstracts From the 2018 International Neuroethics Society Annual Meeting
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  60. Human Subjects Research Without Consent: Duties to Return Individual Findings When Participation was Non-Consensual
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  66. Excluded, not dismissed: Enhancing benefit in clinical research
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  71. 5. Genetic Research With Minority Populations
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  74. Policy Needs Regarding the Duty to Protect in Epidemiological Research with High-Risk Populations
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  75. Ancillary Care Obligations for Social Media Platforms
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  76. Ethical considerations around volunteer payments in a malaria Human Infection Study in Kenya: An embedded empirical ethics study
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  77. Incorporating Research Burden and Utility Considerations as Limiting Factors in a Framework for Returning IRR
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  78. La investigación y los conflictos de interés: Una mirada a vuelo de pájaro
    Jorge Luis Manrique, Susana N. Torres, Mariana Andrijic, Alberto Combi · 2015 · Inmanencia. Revista del Hospital Interzonal General de Agudos (HIGA) Eva Perón
  79. Ancillary‐Care Obligations
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  80. El medico y la investigación clínica
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  81. The Investigator-Participant Relationship—Reply
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  82. Exploitation and biomedical research in the developing world
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  83. A Critical Assessment of the Work of Research Ethics Committees.
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  84. Informed Consent for Research Using Biospecimens, Genetic Information and Other Personal Data
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  89. Informed Consent for Research Using Biospecimens, Genetic Information and Other Personal Data
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  90. Ethical Issues in International Research
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  91. Benefits
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  92. Risks
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  93. Informed Consent for Research Using Biospecimens, Genetic Information and Other Personal Data
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  95. Scientific Research and Ethics
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  96. Authorship
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  97. Data Acquisition and Management
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  98. Conclusion
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  99. Mentoring and the Research Environment
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  100. The Protection of Human Subjects in Research
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