Christine Grady mainly focuses on Informed consent, MEDLINE, Health care, Clinical trial and Nursing. Her Informed consent research is multidisciplinary, incorporating perspectives in Social psychology, Vulnerability, Bioethics, Research ethics and Beneficence. In her study, Professional ethics is inextricably linked to Inclusion, which falls within the broad field of Beneficence.
Her MEDLINE study integrates concerns from other disciplines, such as Clinical research, Payment, Pediatric research, Inclusion and Empirical research. Her Health care research includes elements of Developing country, Quality and Professional association. Her work carried out in the field of Clinical trial brings together such families of science as Helsinki declaration, Response rate, Therapeutic misconception and Risk assessment.
Christine Grady spends much of her time researching Informed consent, Family medicine, Clinical trial, Nursing and MEDLINE. In her research, Harm and Law is intimately related to Research ethics, which falls under the overarching field of Informed consent. Her Family medicine research incorporates elements of Psychological intervention, Cancer, Consent Forms, Acquired immunodeficiency syndrome and Response rate.
Her study looks at the relationship between Clinical trial and topics such as Alternative medicine, which overlap with Clinical research. She interconnects Social work and Health care in the investigation of issues within Nursing. Her Health care study combines topics from a wide range of disciplines, such as Developing country and Public health.
Christine Grady focuses on Health care, Nursing, MEDLINE, Family medicine and Coronavirus disease 2019. Her studies deal with areas such as Autonomy, Bioethics, Psychiatry and Clinical Ethics as well as Health care. The Nursing study combines topics in areas such as Patient participation, Payment, Moral distress and Ethics education.
The various areas that Christine Grady examines in her MEDLINE study include Clinical trial, Coercion and Informed consent. Her Informed consent research integrates issues from Genetic privacy, Public policy and Medical education. Her studies in Family medicine integrate themes in fields like Cancer, Cancer clinical trial, Clinical research, Disease burden and Transplantation.
The scientist’s investigation covers issues in Health care, Nursing, MEDLINE, Coronavirus disease 2019 and Bioethics. Her Health care study combines topics in areas such as Young adult, Demography, Family medicine, Autonomy and Developing country. Her Nursing research includes themes of Health professions, Qualitative research, Course of illness and Ethics education.
Her research integrates issues of Genetic privacy, Respondent and Public policy in her study of MEDLINE. Her Coronavirus disease 2019 research focuses on Scarcity and how it relates to Global health, Workforce, Pandemic, Nursing ethics and Public relations. Her study in Bioethics is interdisciplinary in nature, drawing from both Brain research, Ethnic group, Cognitive science and Neuroethics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
What Makes Clinical Research Ethical
Ezekiel J. Emanuel;David Wendler;Christine Grady.
What Makes Clinical Research in Developing Countries Ethical? The Benchmarks of Ethical Research
Ezekiel J. Emanuel;David Wendler;Jack Killen;Christine Grady.
The Journal of Infectious Diseases (2004)
Ethical climate, ethics stress, and the job satisfaction of nurses and social workers in the United States.
Connie Ulrich;Patricia O'Donnell;Carol Taylor;Adrienne Farrar.
Social Science & Medicine (2007)
What's the price of a research subject? Approaches to payment for research participation.
Neal Dickert;Christine Grady.
The New England Journal of Medicine (1999)
How Much Is Life Worth: Cetuximab, Non–Small Cell Lung Cancer, and the $440 Billion Question
Tito Fojo;Christine Grady.
Journal of the National Cancer Institute (2009)
Risks and benefits of phase 1 oncology trials, 1991 through 2002.
Elizabeth Horstmann;Mary S. McCabe;Louise Grochow;Seiichiro Yamamoto;Seiichiro Yamamoto.
The New England Journal of Medicine (2005)
Clinical Trials and Medical Care: Defining the Therapeutic Misconception
Gail E Henderson;Larry R Churchill;Arlene M Davis;Michele M Easter.
PLOS Medicine (2007)
The Limitations of “Vulnerability” as a Protection for Human Research Participants
Carol Levine;Ruth Faden;Christine Grady;Dale E Hammerschmidt.
American Journal of Bioethics (2004)
Payment of clinical research subjects
Journal of Clinical Investigation (2005)
Enduring and Emerging Challenges of Informed Consent
The New England Journal of Medicine (2015)
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