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  2. Informed consent - Wikipedia

    en.wikipedia.org/wiki/Informed_consent

    Informed consent is documented by means of a written, signed, and dated informed consent form. [33] In medical research, the Nuremberg Code set a base international standard in 1947, in response to the ethical violation in the Holocaust. Standards continued to develop.

  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. 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.

  5. Glossary of clinical research - Wikipedia

    en.wikipedia.org/wiki/Glossary_of_clinical_research

    Informed consent is documented by means of a written, signed, and dated informed consent form. (ICH E6) Informed consent document A document that describes the rights of the study participants, and includes details about the study, such as its purpose, duration, required procedures, and key contacts. Risks and potential benefits are explained ...

  6. National Commission for the Protection of Human Subjects of ...

    en.wikipedia.org/wiki/National_Commission_for...

    2) assessing the risks and benefits of the appropriateness of research involving human subjects 3) determining appropriate guidelines for how human subjects can be chosen for the participation in such research 4) defining what informed consent is in each research setting.

  7. 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.

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