Libri sul tema "Consent in research"

Glahn, Sandra. Informed consent: A novel. Colorado Springs, CO: David C. Cook, 2007.

Kim, Scott Y. H. Evaluation of capacity to consent to treatment and research. Oxford: Oxford University Press, 2010.

1953-, Smyth Marie, e Williamson Emma, a cura di. Researchers and their "subjects": Ethics, power, knowledge, and consent. Bristol, UK: Policy Press, 2004.

Salmons, Janet, e Kate Orton-Johnson. How to Understand and Gain Informed Consent for Internet Research. 1 Oliver’s Yard, 55 City Road, London EC1Y 1SP United Kingdom: SAGE Publications, Ltd., 2022. http://dx.doi.org/10.4135/9781529608113.

Great Britain. Mental Health Act Commission. Research involving detained patients. Nottingham: The Commission, 1997.

Menikoff, Jerry. Patients at risk: The hidden truth about medical research. New York, N.Y: Oxford University Press, 2006.

American College of Physician Executives., a cura di. Medical risk and the right to an informed consent in clinical care and clinical research. Tampa, Fla: American College of Physician Executives, 1998.

Manipulation and consent: How voters and leaders manage complexity. Vancouver: UBC Press, 1993.

Ellickson, Phyllis L. An assessment of active versus passive methods for obtaining parental consent. [Santa Monica, Calif: Rand Corp.], 1989.

Council for International Organizations of Medical Sciences. e World Health Organization, a cura di. International ethical guidelines for biomedical research involving human subjects. Geneva: CIOMS, 2002.

Research involving persons with mental disorders that may affect decisionmaking capacity. Rockville, Md. (6100 Executive Blvd., Suite 5B01, Rockville 20892-7508): National Bioethics Advisory Commission, 1998.

Tri-Council Working Group on the Ethics of Research Involving Humans (Canada). The ethics of research involving humans. [Toronto]: The Working Group, 1994.

Genetic research on addiction: Ethics, the law, and public health. Cambridge: Cambridge University Press, 2012.

Arscott, Katy J. [Assessing the ability of people with a learning disability to consent to treatment and research]. Birmingham: University of Birmingham, 1996.

Marshall, Patricia Loomis. Ethical challenges in study design and informed consent for health research in resource-poor settings. Geneva, Switzerland: World Health Organization, 2007.

Arscott, Katy J. Assessing the ability of people with a learning disability to consent to treatment and research. Birmingham: University of Birmingham, 1996.

New York (State). Dept. of Health. Advisory Work Group on Human Subject Research Involving the Protected Classes. Recommendations on the oversight of human subject research involving the protected classes. [Albany?]: State of New York Dept. of Health, 1998.

Natural Sciences and Engineering Research Council Canada, Social Sciences and Humanities Research Council of Canada e Interagency Secretariat on Research Ethics (Canada), a cura di. Tri-council policy statement: Ethical conduct for research involving humans. Ottawa: Interagency Secretariat on Research Ethics, 2010.

Price, David P. T. Human tissue in transplantation and research: A model legal and ethical donation framework. Cambridge, UK: Cambridge University Press, 2009.

Bach, Michael. Seeking consent to participate in research from people whose ability to make an informed decision could be questioned: The supported decision-making model. [North York, Ont.]: Roeher Institute, 1996.

Getz, Kenneth. Informed consent: A guide to the risks and benefits of volunteering for clinical trials. Boston, MA: CenterWatch, 2002.

Ethical and legal requirements for transnational genetic research. München: C.H. Beck, 2010.

Mettre en banque l'ADN: Enquête sur une biopolitique du consentement. Paris: L'Harmattan, 2010.

Institute of Medicine (U.S.). Committee on Assessing the System for Protecting Human Research Subjects. Preserving public trust: Accreditation and human research participant protection programs. Washington, D.C: National Academy Press, 2001.

Len, Doyal, e Tobias Jeffrey S, a cura di. Informed consent in medical research. London: BMJ, 2000.

Tobias, Jeffrey. Informed Consent in Medical Research. Blackwell Publishing Limited, 2001.

Sugarman, Jeremy, Jeffrey P. Kahn e Anna Mastroianni. Beyond Consent: Seeking Justice in Research. Oxford University Press, 1998.

Ray, Sumantra (Shumone), Sue Fitzpatrick, Rajna Golubic, Susan Fisher e Sarah Gibbings, a cura di. Informed consent in a research setting. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199608478.003.0009.

P, Kahn Jeffrey, Mastroianni Anna C e Sugarman Jeremy, a cura di. Beyond consent: Seeking justice in research. New York: Oxford University Press, 1998.

(Editor), Jeffrey P. Kahn, Anna C. Mastroianni (Editor) e Jeremy Sugarman (Editor), a cura di. Beyond Consent: Seeking Justice in Research. Oxford University Press, USA, 1998.

Beyond Consent: Seeking Justice in Research. Oxford University Press, Incorporated, 2018.

Glahn, Sandra. Informed Consent. David C. Cook Distribution, 2007.

Alderson, Priscilla. Disabled People and Consent to Medical Treatment and Research (Consent Conference S.). Research & Education Association,U.S., 1993.

Jeremy, Sugarman, e Hastings Center, a cura di. Empirical research on informed consent: An annotated bibliography. [Garison, NY: Hastings Center], 1999.

European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2017.

Megone, Chris, e Su Mason. European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2020.

Megone, Chris, e Su Mason. European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2018.

Megone, Chris, e Su Mason. European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2018.

Megone, Chris, e Su Mason. European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2018.

Megone, Chris, e Su Mason. European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2018.

Megone, Chris, e Su Mason. European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2020.

Megone, Chris, e Su Mason. European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2020.

(Editor), Susan A. Mason, e Chris Megone (Editor), a cura di. European Neonatal Research: Consent, Ethics Committees and Law. Ashgate Publishing, 2001.

Megone, Chris, e Su Mason. European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2020.

Megone, Chris, e Su Mason. European Neonatal Research: Consent, Ethics Committees and Law. Taylor & Francis Group, 2018.

Informed Consent: Information Production and Ideology. The Scarecrow Press, Inc., 2003.

Schiff, Lisa R. Informed Consent: Information Production and Ideology. Scarecrow Press, Incorporated, 2003.

Kim, Scott Y. H. Evaluation of Capacity to Consent to Treatment and Research. Oxford University Press, 2009.

(Editor), Marie Smyth, e Emma Williamson (Editor), a cura di. Researchers and Their 'Subjects': Ethics, Power, Knowledge and Consent. Policy Press, 2004.

Researchers and Their 'Subjects': Ethics, Power, Knowledge and Consent. Policy Press, 2004.