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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. Free, prior and informed consent - Wikipedia

    en.wikipedia.org/wiki/Free,_prior_and_informed...

    Consent is not defined but is granted or withheld after a process that involves consultation and participation. However, mere consultation by itself is not a substitute for actual consent. [5] The UN Working Group on Business and Human Rights notes that Indigenous Peoples "should determine autonomously how they define and establish consent." [6]

  4. Conscience clause in medicine in the United States - Wikipedia

    en.wikipedia.org/wiki/Conscience_clause_in...

    An informed consent clause, although allowing medical professionals not to perform procedures against their conscience, does not allow professionals to give fraudulent information to deter a patient from obtaining such a procedure (such as lying about the risks involved in an abortion to deter one from obtaining one) in order to impose one's belief using deception.

  5. Right to know - Wikipedia

    en.wikipedia.org/wiki/Right_to_know

    Right to know is a human right enshrined in law in several countries. UNESCO defines it as the right for people to "participate in an informed way in decisions that affect them, while also holding governments and others accountable". [1]

  6. 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.

  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.