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Rosemarie D. L. C. Bernabe [5]Rose Bernabe [1]Rosemarie Bernabe [1]Rosemarie Dlc Bernabe [1]
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  1.  11
    Back to WHAT? The Role of Research Ethics in Pandemic Times.Jan Helge Solbakk, Heidi Beate Bentzen, Søren Holm, Anne Kari Tolo Heggestad, Bjørn Hofmann, Annette Robertsen, Anne Hambro Alnæs, Shereen Cox, Reidar Pedersen & Rose Bernabe - 2021 - Medicine, Health Care and Philosophy 24 (1):3-20.
    The Covid-19 pandemic creates an unprecedented threatening situation worldwide with an urgent need for critical reflection and new knowledge production, but also a need for imminent action despite prevailing knowledge gaps and multilevel uncertainty. With regard to the role of research ethics in these pandemic times some argue in favor of exceptionalism, others, including the authors of this paper, emphasize the urgent need to remain committed to core ethical principles and fundamental human rights obligations all reflected in research regulations and (...)
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  2. News Media Coverage of Euthanasia: A Content Analysis of Dutch National Newspapers. [REVIEW]Rosemarie D. L. C. Bernabe, Ghislaine J. M. W. Van Thiel, Jan A. M. Raaijmakers & Johannes J. M. Van Delden - 2013 - BMC Medical Ethics 14 (1):6-.
    BackgroundThe Netherlands is one of the few countries where euthanasia is legal under strict conditions. This study investigates whether Dutch newspaper articles use the term ‘euthanasia’ according to the legal definition and determines what arguments for and against euthanasia they contain.MethodsWe did an electronic search of seven Dutch national newspapers between January 2009 and May 2010 and conducted a content analysis.ResultsOf the 284 articles containing the term ‘euthanasia’, 24% referred to practices outside the scope of the law, mostly relating to (...)
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  3.  37
    The Fiduciary Obligation of the Physician-Researcher in Phase IV Trials.Rosemarie Dlc Bernabe, Ghislaine Jmw van Thiel, Jan Am Raaijmakers & Johannes Jm van Delden - 2014 - BMC Medical Ethics 15 (1):11.
    BackgroundIn this manuscript, we argue that within the context of phase IV, physician-researchers retain their fiduciary obligation to treat the patient-participants.DiscussionWe first clarify why the perspective that research ethics ought to be differentiated from clinical ethics is not applicable in phase IV, and therefore, why therapeutic orientation is most convivial in this phase. Next, assuming that ethics guidelines may be representative of common morality, we show that ethics guidelines see physician-researchers primarily as physicians and only secondarily as researchers. We then (...)
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  4.  29
    What Do International Ethics Guidelines Say in Terms of the Scope of Medical Research Ethics?Rosemarie D. L. C. Bernabe, Ghislaine J. M. W. van Thiel & Johannes J. M. van Delden - 2016 - BMC Medical Ethics 17 (1):1-18.
    BackgroundIn research ethics, the most basic question would always be, “which is an ethical issue, which is not?” Interestingly, depending on which ethics guideline we consult, we may have various answers to this question. Though we already have several international ethics guidelines for biomedical research involving human participants, ironically, we do not have a harmonized document which tells us what these various guidelines say and shows us the areas of consensus. In this manuscript, we attempted to do just that.MethodsWe extracted (...)
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  5.  21
    The Need to Explicate the Ethical Evaluation Tools to Avoid Ethical Inflation.Rosemarie Bernabe, Ghislaine van Thiel, Jan Raaijmakers & Johannes van Delden - 2009 - American Journal of Bioethics 9 (11):56-58.
  6.  3
    Composition and Capacity of Institutional Review Boards, and Challenges Experienced by Members in Ethics Review Processes in Addis Ababa, Ethiopia: An Exploratory Qualitative Study.Yemisrach Zewdie Seralegne, Cynthia Khamala Wangamati, Rosemarie D. L. C. Bernabe, Bobbie Farsides, Abraham Aseffa & Martha Zewdie - forthcoming - Developing World Bioethics.
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  7.  16
    Ethics and the Marketing Authorization of Pharmaceuticals: What Happens to Ethical Issues Discovered Post-Trial and Pre-Marketing Authorization?Rosemarie D. L. C. Bernabe, Ghislaine J. M. W. van Thiel, Nancy S. Breekveldt, Christine C. Gispen & Johannes J. M. van Delden - 2020 - BMC Medical Ethics 21 (1):1-8.
    Background In the EU, clinical assessors, rapporteurs and the Committee for Medicinal Products for Human Use are obliged to assess the ethical aspects of a clinical development program and include major ethical flaws in the marketing authorization deliberation processes. To this date, we know very little about the manner that these regulators put this obligation into action. In this paper, we intend to look into the manner and the extent that ethical issues discovered during inspection have reached the deliberation processes. (...)
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    Composition and Capacity of Institutional Review Boards, and Challenges Experienced by Members in Ethics Review Processes in Addis Ababa, Ethiopia: An Exploratory Qualitative Study.Yemisrach Zewdie Seralegne, Cynthia Khamala Wangamati, Rosemarie D. L. C. Bernabe, Bobbie Farsides, Abraham Aseffa & Martha Zewdie - forthcoming - Wiley: Developing World Bioethics.
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