Saltar al contenido principal

ETHNOS_APP

Inicio • Búsqueda • Revistas • Lista 0

Liza Dawson

Datos Biográficos

ID3930069
NOMBRELiza Dawson
NOMBRESLiza
APELLIDODawson
FIRMADAWSON L
AFILIACIONESJohns Hopkins University
ORCID0000-0002-0980-4107
VERIFICADOSí
TOTAL DE OBRAS7
TOTAL DE CITAS18
TOTAL COMO AUTOR7
TOTAL COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN2003
AÑO MÁS RECIENTE DE PUBLICACIÓN2026
ÍNDICE H1
  • Establishing Clinical Trial Priorities for Military Global Health Research

    Open Access•Liza Dawson, Hunter Jackson Smith et al.•ARTICLE•Developing World Bioethics•2026

    Military leaders must support health care and research to protect the health and readiness of their forces. Part of this effort entails conducting human subjects research to address current and emerging international health threats. The military is also attentive to the national security interests associated with global health, such as protection from widespread disruption due to disasters and epidemics. While military leaders’ global health rese…

  • Using an Equivalent Protections Framework to Improve Oversight of International Human Subjects Research

    Open Access•Liza Dawson, Hunter Jackson Smith•ARTICLE•Developing World Bioethics•2026

    Current US military international research protocols involving human subjects are reviewed, approved, and overseen by both US and regulatory bodies. In some cases host nation research partners are disadvantaged due to slower processing times and redundant protocol reviews when competing for opportunities to conduct clinical trials. This article considers international legal and regulatory tensions between protecting host nations’ patient‐subjects…

  • Understanding the ‘De Jure’ Standard of Care for Research

    Open Access•Liza Dawson, Adnan A Hyder•ARTICLE•Developing World Bioethics•2007

  • Defining Standard of Care in the Developing World

    Open Access•Adnan A Hyder, Liza Dawson•ARTICLE•Developing World Bioethics•2005

    In recent years there has been intense debate regarding the level of medical care provided to 'standard care' control groups in clinical trials in developing countries, particularly when the research sponsors come from wealthier countries. The debate revolves around the issue of how to define a standard of medical care in a country in which many people are not receiving the best methods of medical care available in other settings. In this paper, …

  • Views of US researchers about informed consent in international collaborative research

    Open Access•Liza Dawson, Norman Ka et al.•ARTICLE•Social Science & Medicine•2005•Citada por: 18•Referencias: 15

  • Public Stem Cell Banks

    Ruth Faden, Ruth R Faden et al.•ARTICLE•The Hastings Center Report•2003

    Ruth R. Faden, Liza Dawson, Alison S. Bateman-House, Dawn Mueller Agnew, Hilary Bok, Dan W. Brock, Aravinda Chakravarti, Xiao-Jiang Gao, Mark Greene, John A. Hansen, Patricia A. King, Stephen J. O'Brien, David H. Sachs, Kathryn E. Schill, Andrew Siegel, Davor Solter, Sonia M. Suter, Catherine M. Verfaillie, LeRoy B. Walters, John D. Gearhart, Public Stem Cell Banks: Considerations of Justice in Stem Cell Research and Therapy, The Hastings Center …

  • Ethical Oversight of Research in Developing Countries

    Norman Ka, Nancy Kass et al.•ARTICLE•IRB Ethics and Human Research•2003

    by private companies on products that are regulated by the Food and Drug Administration must adhere to FDA regulations (2z CFR 50, 56), which require review by a single IRB, but do not specify where that IRB must be located. (Studies conducted for reasons other than marketing approval need not undergo ethics review.) The International Conference on Harmonisation's guidelines are frequently used for private research carried out in industrialized

  • Views of US researchers about informed consent in international collaborative research

    Open Access•Liza Dawson, Norman Ka et al.•ARTICLE•Social Science & Medicine•2005•Citada por: 18•Referencias: 15

  • Public Stem Cell Banks

    Ruth Faden, Ruth R Faden et al.•ARTICLE•The Hastings Center Report•2003

    Ruth R. Faden, Liza Dawson, Alison S. Bateman-House, Dawn Mueller Agnew, Hilary Bok, Dan W. Brock, Aravinda Chakravarti, Xiao-Jiang Gao, Mark Greene, John A. Hansen, Patricia A. King, Stephen J. O'Brien, David H. Sachs, Kathryn E. Schill, Andrew Siegel, Davor Solter, Sonia M. Suter, Catherine M. Verfaillie, LeRoy B. Walters, John D. Gearhart, Public Stem Cell Banks: Considerations of Justice in Stem Cell Research and Therapy, The Hastings Center …

  • Ethical Oversight of Research in Developing Countries

    Norman Ka, Nancy Kass et al.•ARTICLE•IRB Ethics and Human Research•2003

    by private companies on products that are regulated by the Food and Drug Administration must adhere to FDA regulations (2z CFR 50, 56), which require review by a single IRB, but do not specify where that IRB must be located. (Studies conducted for reasons other than marketing approval need not undergo ethics review.) The International Conference on Harmonisation's guidelines are frequently used for private research carried out in industrialized

  • Defining Standard of Care in the Developing World

    Open Access•Adnan A Hyder, Liza Dawson•ARTICLE•Developing World Bioethics•2005

    In recent years there has been intense debate regarding the level of medical care provided to 'standard care' control groups in clinical trials in developing countries, particularly when the research sponsors come from wealthier countries. The debate revolves around the issue of how to define a standard of medical care in a country in which many people are not receiving the best methods of medical care available in other settings. In this paper, …

  • Views of US researchers about informed consent in international collaborative research

    Open Access•Liza Dawson, Norman Ka et al.•ARTICLE•Social Science & Medicine•2005•Citada por: 18•Referencias: 15

  • Understanding the ‘De Jure’ Standard of Care for Research

    Open Access•Liza Dawson, Adnan A Hyder•ARTICLE•Developing World Bioethics•2007

  • Establishing Clinical Trial Priorities for Military Global Health Research

    Open Access•Liza Dawson, Hunter Jackson Smith et al.•ARTICLE•Developing World Bioethics•2026

    Military leaders must support health care and research to protect the health and readiness of their forces. Part of this effort entails conducting human subjects research to address current and emerging international health threats. The military is also attentive to the national security interests associated with global health, such as protection from widespread disruption due to disasters and epidemics. While military leaders’ global health rese…

  • Using an Equivalent Protections Framework to Improve Oversight of International Human Subjects Research

    Open Access•Liza Dawson, Hunter Jackson Smith•ARTICLE•Developing World Bioethics•2026

    Current US military international research protocols involving human subjects are reviewed, approved, and overseen by both US and regulatory bodies. In some cases host nation research partners are disadvantaged due to slower processing times and redundant protocol reviews when competing for opportunities to conduct clinical trials. This article considers international legal and regulatory tensions between protecting host nations’ patient‐subjects…

Ethics in Clinical Research (5 obras) · Political science (5 obras) · Research ethics (4 obras) · Biomedical Ethics and Regulation (3 obras) · Health Systems, Economic Evaluations, Quality of Life (3 obras) · Law (3 obras) · Medicine (3 obras) · Developing country (2 obras) · Economic growth (2 obras) · Economics (2 obras)

Ethnos_APP • Proyecto Open Source • Licencia MIT • Frontend v2.0.0 • Privacidad y Cookies • Documentación de la API: api.ethnos.app/docs • Código de la API: GitHub • DOI: 10.5281/zenodo.17049435 • Código del Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae