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  2. Informed consent - Wikipedia

    en.wikipedia.org/wiki/Informed_consent

    Informed consent is a technical term first used by attorney, Paul G. Gebhard, in the Salgo v. Leland Stanford Jr. University Board of Trustees court case in 1957. [50] In tracing its history, some scholars have suggested tracing the history of checking for any of these practices: [51]: 54

  3. 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.

  4. Nuremberg Code - Wikipedia

    en.wikipedia.org/wiki/Nuremberg_Code

    The Nuremberg Code (German: Nürnberger Kodex) is a set of ethical research principles for human experimentation created by the court in U.S. v Brandt, one of the Subsequent Nuremberg trials that were held after the Second World War.

  5. Informed assent - Wikipedia

    en.wikipedia.org/wiki/Informed_assent

    A child over 14 years old may be able to provide their own informed consent, independent of their parents. [13] The legal precedent is that as an emancipated minor they may consent to any medical procedure they see fit (E.g., Carter v. Cangello, 105 Cal App 3d 348, 164 Cal Rptr 361, 1980; Lacey v.

  6. Common Rule - Wikipedia

    en.wikipedia.org/wiki/Common_rule

    The Common Rule is a 1991 rule of ethics (revised in 2018) [2] regarding biomedical and behavioral research involving human subjects in the United States.The regulations governing Institutional Review Boards for oversight of human research followed the 1975 revision of the Declaration of Helsinki, and are encapsulated in the 1991 revision to the U.S. Department of Health and Human Services ...

  7. Title 21 CFR Part 11 - Wikipedia

    en.wikipedia.org/wiki/Title_21_CFR_Part_11

    Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES).

  8. Implied consent - Wikipedia

    en.wikipedia.org/wiki/Implied_consent

    Specifically addressing implied consent laws, the court in the Birchfield opinion stated that while their "prior opinions have referred approvingly to the general concept of implied-consent laws" that "there must be a limit to the consequences to which motorists may be deemed to have consented by virtue of a decision to drive on public roads ...

  9. Talk:Informed consent - Wikipedia

    en.wikipedia.org/wiki/Talk:Informed_consent

    Unfortunately, it is uncited and surrounded by material that is made up. The legal definition of informed consent is "A person's agreement to allow something to happen, made with full knowledge of the risks involved and the alternatives. • For the legal profession, informed consent is defined in Model Rule of Professional Conduct 1.0(e). 2.