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2. Informed consent - Wikipedia

   en.wikipedia.org/wiki/Informed_consent

   Example of informed consent document from the PARAMOUNT trial. Informed consent is a principle in medical ethics, medical law, media studies, and other fields, that a person must have sufficient information and understanding before making decisions about accepting risk, such as their medical care.

3. Dynamic consent - Wikipedia

   en.wikipedia.org/wiki/Dynamic_consent

   Dynamic consent is an approach to informed consent that enables on-going engagement and communication between individuals and the users and custodians of their data. It is designed to address the many issues that are raised by the use of digital technologies in research and clinical care that enable the wide-scale use, linkage, analysis and integration of diverse datasets and the use of AI and ...

4. Unethical human experimentation - Wikipedia

   en.wikipedia.org/wiki/Unethical_human...

   Beecher believed that rules requiring informed consent were not alone sufficient, as truly informed consent was an unattainable ideal. He worked both to define the rules and conditions for informed consent, and to establish institutional review boards as an additional layer of oversight regarding research protocols. [74] [75]

5. Informed Consent in Medical Research - Wikipedia

   en.wikipedia.org/wiki/Informed_Consent_in...

   Informed Consent in Medical Research is a medical textbook on medical ethics, authored by Jeffrey S. Tobias and Len Doyal, and published by Wiley in 2001. It was produced in response to the debates between the authors in 1997, following the response to the 1990's British Medical Journal publications of studies in which consent was not obtained by participants.

6. Belmont Report - Wikipedia

   en.wikipedia.org/wiki/Belmont_Report

   The Belmont Report is a 1978 report created by the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research.Its full title is the Belmont Report: Ethical Principles and Guidelines for the Protection of Human Subjects of Research, Report of the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research.

7. The Regulation Of This Acne Drug Is Eerily Similar To Project ...

   www.aol.com/feel-just-registered-uterus...

   Then you’ll read through and sign pages of informed consent forms, a standard practice for many drugs with significant risks and side effects. ... for example—this could mean you have to delay ...