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  2. Institutional review board - Wikipedia

    en.wikipedia.org/wiki/Institutional_review_board

    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 ...

  3. Employee monitoring - Wikipedia

    en.wikipedia.org/wiki/Employee_monitoring

    Employee monitoring is the (often automated) surveillance of workers' activity. Organizations engage in employee monitoring for different reasons such as to track performance, to avoid legal liability, to protect trade secrets, and to address other security concerns. [1] This practice may impact employee satisfaction due to its impact on the ...

  4. Belmont Report - Wikipedia

    en.wikipedia.org/wiki/Belmont_Report

    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 ...

  5. Data monitoring committee - Wikipedia

    en.wikipedia.org/wiki/Data_Monitoring_Committee

    Data monitoring committee. (Redirected from Data Monitoring Committee) An early recipient of the COVID-19 vaccine. A data monitoring committee ( DMC) – sometimes called a data and safety monitoring board ( DSMB) – is an independent group of experts who monitor patient safety and treatment efficacy data while a clinical trial is ongoing.

  6. Monitoring in clinical trials - Wikipedia

    en.wikipedia.org/wiki/Monitoring_in_clinical_trials

    Clinical monitoring is the oversight and administrative efforts that monitor a participant's health and efficacy of the treatment during a clinical trial.Both independent and government-run grant-funding agencies, such as the National Institutes of Health (NIH) and the World Health Organization (WHO), require data and safety monitoring protocols for Phase I and II clinical trials conforming to ...

  7. Good clinical practice - Wikipedia

    en.wikipedia.org/wiki/Good_Clinical_Practice

    Good clinical practice ( GCP) is an international quality standard, which governments can then transpose into regulations for clinical trials involving human subjects. GCP follows the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), and enforces tight guidelines on ethical aspects of ...

  8. Research ethics - Wikipedia

    en.wikipedia.org/wiki/Research_ethics

    Research ethics is a discipline within the study of applied ethics. Its scope ranges from general scientific integrity and misconduct to the treatment of human and animal subjects. The societal responsibilities science and research has are not traditionally included and less well defined.

  9. APA Ethics Code - Wikipedia

    en.wikipedia.org/wiki/APA_Ethics_Code

    APA Ethics Code. The American Psychological Association (APA) Ethical Principles of Psychologists and Code of Conduct (for short, the Ethics Code, as referred to by the APA) includes an introduction, preamble, a list of five aspirational principles and a list of ten enforceable standards that psychologists use to guide ethical decisions in ...