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  2. Institutional review board - Wikipedia

    en.wikipedia.org/wiki/Institutional_review_board

    An institutional review board (IRB), also known as an independent ethics committee (IEC), ethical review board (ERB), or research ethics board (REB), is a committee at an institution that applies research ethics by reviewing the methods proposed for research involving human subjects, to ensure that the projects are ethical. The main goal of IRB ...

  3. Human subject research legislation in the United States

    en.wikipedia.org/wiki/Human_subject_research...

    [6] [14] The Commission work from 1974-1978 resulted in 17 reports and appendices, of which the most important were the Institutional Review Board Report and the Belmont Report ("Ethical Principles and Guidelines for the Protection of Human Subjects of Research"). [3] [14] The IRB Report endorsed the establishment and functioning of the ...

  4. Ethics committee - Wikipedia

    en.wikipedia.org/wiki/Ethics_committee

    In the United States, an ethics committee is usually known as an institutional review board (IRB) or research ethics board (REB) and is dedicated to overseeing the rights and well-being of research subjects participating in scientific studies in the US. Similarly in Canada, the committee is called a Research Ethics Board (REB).

  5. Office for Human Research Protections - Wikipedia

    en.wikipedia.org/wiki/Office_for_Human_Research...

    An institutional review board (IRB) is a type of committee that reviews human based bio-research. Under 45 C.F.R 46, each IRB that is designated by an institution must be registered with the Office for Human Research Protections (OHRP) of the Department of Health and Human Services (HHS). When registering an IRB, the following information must ...

  6. Belmont Report - Wikipedia

    en.wikipedia.org/wiki/Belmont_Report

    The Belmont Report allows for the protection of participants in clinical trials and research studies. Seven things nurses, as primary caregivers for individuals participating in a study, must do to ensure the rights of the participant are met are. [9] Ensure the study is approved by an IRB; Get informed consent from the patient

  7. Human subject research - Wikipedia

    en.wikipedia.org/wiki/Human_subject_research

    Medical human subject research often involves analysis of biological specimens, epidemiological and behavioral studies and medical chart review studies. [1] A specific, and especially heavily regulated, type of medical human subject research is the " clinical trial ", in which drugs, vaccines and medical devices are evaluated.)

  8. Certified IRB Professional - Wikipedia

    en.wikipedia.org/wiki/Certified_IRB_Professional

    The Certified IRB Professional (CIP) program is a certification initiative in the United States for individuals administering and overseeing the daily activities of institutional review boards (IRBs). IRBs are committees that are charged with determining if a research project conforms to ethical principles and federal regulations that protect ...

  9. Guidelines for human subject research - Wikipedia

    en.wikipedia.org/wiki/Guidelines_for_human...

    The study was influential in shaping public perceptions of research involving human subjects. After the press exposed the study, the US Congress appointed a panel that determined that the study should be stopped immediately and that the oversight of human research was inadequate. The panel recommended that federal regulations be designed and ...

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